Patentkrav

1. Forbindelse eller salt deraf med formel (I):





fl l OR 1 x' "u 2

0

hvor:

Ri er H eller -C(0 )Ri, R4 er hydrogen, alkyl, cycloalkyl,

alkenyl, alkynyl, aryl, alkyaryl, arylakyl, arylalkenyl,



arylalkynyl og heterocyklisk;

R3 er hydrogen, R2 er substitueret alkyl, der har i intervallet fra 1 op til 8 carbonatomer, hvor substituenten er -NR7R8, og dens farmaceutisk acceptable salte dannet med uorganisk og/eller organisk syre og inklusive dens kvaternære ammoniumsalte dannet med R9Z;

hvor R7 og Rg er udvalgt blandt hydrogen, alkyl, der har i intervallet fra 1 op til 8 carbonatomer, eller cycloalkyl;

Z er fluor, chlor, brom, iod, tosylat, methansulfonat, benzensulfonat,    trifluormethansulfonat,    R9 er alkyl,

cycloalkyl, alkyl substitueret med hydroxyl, alkenyl, alkynyl, aryl, heterocyklisk, arylakyl, arylalkenyl, arylalkynyl, cyanomethyl, alkoxy eller aryloxyalkyl; den uorganiske eller organiske syre er flussyre, saltsyre, brombrintesyre, iodbrintesyre, svovlsyre, salpetersyre, phosphorsyre, carbonsyre, borsyre, selensyrling, phosphormolybdænsyre, phosphorsyre, svovlsyrling, citronsyre, maleinsyre, D-æblesyre, L-æblesyre, DL-æblesyre, L-mælkesyre, D-mælkesyre, DL-mælkesyre, oxalsyre, methansulfonsyre, valerianesyre, oleinsyre,      laurinsyre,      para-toluensulfonsyre,      1-

naphthalensulfonsyre, 2-naphthalensulfonsyre, phthalsyre, vinsyre, malonsyre, ravsyre, fumarsyre, glycolsyre, thioglycolsyre, glycin, sarcocin, sulfonsyre, nicotinsyre, picolinsyre, isonicotinsyre og benzoesyre;

X er 0;

Y er en enkeltbinding, 0, RuN, R12R13C, Ru er hydrogen, alkyl,

cycloalkyl, alkenyl, alkynyl, aryl, alkyaryl, arylalkyl, arylalkenyl, arylalkynyl eller heterocyklisk; R12 og R13 er ens eller forskellige, de er hydrogen, fluor, chlor, brom, iod, alkyl, cycloalkyl, alkyl substitueret med hydroxyl, alkenyl, alkynyl, aryl, heterocyklisk, arylakyl, arylalkenyl, arylalkynyl, cyanomethyl, alkoxy eller aryloxyalkyl.

2. Forbindelse eller salt deraf ifølge krav 1, hvor R2 er

methylen substitueret med -NR7R8,

hvor R7 og

Rs

er udvalgt

blandt hydrogen, alkyl,

der har i intervallet fra 1 op til 8

carbonatomer, eller cycloalkyl.

3. Forbindelse eller salt deraf ifølge krav 1, hvor formel

(I) repræsenteres af formel (II),

O

(II) , eller formel (V)

O

HCI

(V)

Fremgangsmåde til fremstilling af en forbindelse eller et deraf

med formel (I), der indbefatter:

4 .

salt

katalysator til

(1)

af micheliolid som materiale, tilsætning af reaktion af det 

organisk opløsningsmiddel og organiske opløsningsmiddel med katalysatoren der har den tilsvarende gruppe eller struktur,

og materialet, til opnåelse af

målforbindeIsen.

5. Fremgangsmåde til fremstilling af et micheliolidderivat med formel (II), der omfatter: reaktion af materialer til opnåelse af forbindelsen med formel (II),

hvor materialerne er micheliolid og dimethylamin.

6. Fremgangsmåde til fremstilling af en forbindelse med formel (V), der omfatter: opløsning af materiale i CH2CI2, hvor materialet er en forbindelse med formel (II);

justering af pH til 4-5 ved anvendelse af saltsyre;

lyofilisering af den vandige opløsning til opnåelse af forbindelsen med formel (V)

7.   Forbindelse eller salt deraf med formel (I) ifølge et hvilket som helst af kravene 1 til 3 til anvendelse i en fremgangsmåde til behandling af cancer, hvor canceren omfatter leukæmi, brystcancer, prostatacancer, nasofaryngealt karcinom, kolorektal cancer, lungecancer, levercancer, øsofagealt karcinom, gastrisk cancer, intestinal cancer, renalt karcinom, mundhulecancer, Hodgkins lymfom, pankreascancer, kolorektal cancer, cervikal cancer, non-Hodgkins lymfom, gliomer, melanom, blærekarcinom, ovariecancer, thyreoideakarcinom, sarkom.

8.   Forbindelse eller salt deraf med formel (I) ifølge et hvilket som helst af kravene 1 til 3 til anvendelse som en medicin.

9.   Farmaceutisk sammensætning, der omfatter en forbindelse eller et salt deraf med formel (I) ifølge et hvilket som helst af kravene 1 til 3.

10.  Farmaceutisk sammensætning, der omfatter en forbindelse eller et salt deraf med formel (I) ifølge et hvilket som helst af kravene 1 til 3 til anvendelse som en medicin.

11.  Farmaceutisk sammensætning til anvendelse i en fremgangsmåde til behandling af cancer, der omfatter en effektiv mængde af en forbindelse eller et salt deraf med formel (I) ifølge et hvilket som helst af kravene 1 til 3 i kombination med et farmaceutisk acceptabelt bæremateriale eller et andet anticancerlægemiddel.

DESCRIPTION

FIELD OF THE INVENTION

[0001] The present invention relates to pharmaceutical technology, and more specifically, relates to micheliolide derivatives or salt thereof, and pharmaceutical composition using which as the effective ingredient for the cancer treatment or auxiliary swelling treatment, producing methods thereof, and the compounds or composition for use in a method of treatment of cancer.

BACKGROUND OF THE INVENTION

[0002] Tumor threats the human health seriously. There are about 200 million cancer patients in China and the number is added by 1.6 million per year, which is a big group. The anti-cancer research is a challenging and significant field in life science and technology. At present, the commonly used clinical anti-cancer drugs are cytotoxic drugs. The characteristics of these drugs are poor selectivity, strong side effects, drug resistance and so on. They are a typical double-edged sword drugs, and difficult to eradicate cancer, which result in high proportion of cancer recurrence. The high rate of the recurrence of cancer has troubled the doctors, and more and more studies confirm that there are a few tumor stem cells in the tumor cell population which can amplify the cell groups. Tumor stem cells are usually in a slow cycle status and have low sensitivity to chemotherapeutic drugs. They are the source of tumor recurrence. The found of the tumor stem cell makes a new target for cancer treatment, and the drug research focused on the tumor stem cell may be able to cure cancer completely.

[0003] In recent years, investigations on anti-cancer compounds from natural products have become the hotspot of anti-cancer drug development. For the past 20 years, 61% newsmall molecule entities drugs may be derived from natural products. Natural products are very common in some therapeutic areas: 78% of the antibacterial compounds and 74% of anti-tumor compounds are natural products or derived from natural products. Practice has proved that the unique role of natural products in anticancer drug discovery re-attach great attention. The traditional treatment of cancer chemotherapy drug have resistance problem, especially the low sensitivity to tumor stem cells. Traditional Chinese medicine (TCM) is profound in anti-cancer field, high efficiency and low toxicity. Accordingly, there is high chance to find drugs eradicating cancer stem cells for cure of malignant tumor from TCM.

[0004] Parthenolide, a sesquiterpene lactone extracted from Tanacetum Parthenium, was originally used to treat skin infections, rheumatism, and migraine. Recent studies have shown that parthenolide can inhibit the growth of cancer cells, such as prostate cancer, breast cancer, gastric cancer, leukemia, kidney cancer, lung cancer, colon adenocarcinoma, and medulloblastoma. Furthermore, parthenolide is effective on treatment of UV-induced skin cancer in animal model. The study of its mechanism finds that parthenolide can inhibit the activation of the transcription factor NF-kB. The activity was mainly derived from the thiol on the subunit of p65/NF-KB which conducts Michael addition reaction with parthenolide. NF-kB is a key gene to regulate tumor invasion, metastasis, and drug resistance genes; therefore, inhibition of NF-kB activation may increase the sensitivity of tumor apoptosis to tumor inhibitor. Recently, Ph.D. Jordan, C. T. and his colleagues found that parthenolide can selectively eliminate cancer stem cells without damage of normal stem cells, which make it possible to suppress recurrence AML. This unique mechanism action of parthenolide has attracted widespread attention.

[0005] Micheliolide belongs to guaiane-type sesquiterpene lacones. It has been reported in the literature [J. Nat. Prod. 1993, 56, 90-98; Bioorg. Med. Chem. Lett. 2003, 11, 1503-1510], On the basis of the results, the present invention reports the use of micheliolide derivatives and its salts in the cancer treatment.

SUMMARY OF THE INVENTION

[0006] The embodiments of present invention provides micheliolide derivative, an anti-cancer pharmaceutical composition comprising an effective amount of micheliolide derivative formula (I) or their salts, methods of preparing them, and micheliolide derivatives of formula (I) or their salts for use in a method of treatment of cancer.

[0007] To achieve the above-mentioned objectives, technical scheme provided includes:

A compound or salt thereof of formula (I) is provided,

«2

O

Wherein:

Ri is H, or -C(O)R4, R4 is hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, aryl, alkyaryl, arylakyl, arylalkenyl, arylalkynyl and heterocyclic;

R3 is hydrogen, R2 is substituted alkyl having in the range of 1 up to 8 carbon atoms, where substituent is -NRyRg, and its pharmaceutically acceptable salts formed with inorganic and/or organic acid, and including its quaternary ammonium salts formed with R9Z. Preferred substituents is methylene substituted by -NR/Rg;

where Ry and Rg are the same or different, they are selected from hydrogen, alkyl having in the range of 1 up to 8 carbon atoms, or cycloalkyl;

Z is fluorine, chlorine, bromine, iodine, tosylate, methanesulfonate, benzenesulfonate, trifluoromethanesulfonate, R9 is alkyl, cycloalkyl, alkyl substituted by hydroxyl,alkenyl, alkynyl, aryl, heterocyclic, arylakyl, arylalkenyl, arylalkynyl, cyanomethyl, alkoxy or aryloxyalkyl ; inorganic or organic acid are hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydriodic acid, sulfuric acid, nitric acid, phosphoric acid, carbonic acid, boric acid, selenious acid, phosphomolybdic acid, phosphorous acid, sulfurous acid, citric acid, maleic acid, D-malic acid, L-malic acid, DL-malic acid, L-lactic acid, D-lactic acid, DL-lactic acid, oxalic acid, methanesulfonic acid, valeric acid, oleic acid, lauric acid, para-toluenesulfonic acid, 1-naphthalensulfonic acid, 2-naphthalensulfonic acid, phthalic acid, tartaric acid, malonic acid, succinic acid, fumaric acid, glycolic acid, thioglycolic acid, glycine, sarcocine, sulfonic acid, nicotinic acid, picolinic acid, isonicotinic acid, benzoic acid and substituted benzoic acid;

Xis O;

Y is single bond, O, R-|-|N, R12R13C, R-|-| is hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, aryl, alkyaryl, arylakyl, arylalkenyl, arylalkynyl or heterocyclic; R12 and R13 are the same or different, they are hydrogen, fluorine, chlorine, bromine, iodine, alkyl, cycloalkyl, alkyl substituted by hydroxyl,alkenyl, alkynyl, aryl, heterocyclic, arylalkyl, arylalkenyl, arylalkynyl, cyanomethyl, alkoxy or aryloxyalkyl.

[0008] Preferably, R2 is methylene substituted by -NR/Rg, where R7 and Rg are the same or different, they are selected from hydrogen, alkyl having in the range of 1 up to 8 carbon atoms, or cycloalkyl.

[0009] The invention also provide a method of producing a compound or salt thereof of formula (I), including: considering nucheliolide as material, adding catalyst into organic solvent, and reacting the organic solvent with the catalyst and the material having the corresponding group or structure to obtain the target compound.

[0010] Preferably, a compound or salt thereof of formula (I) is represented by formula (II), or formula (V)

N— * HCI

[0011] Specifically, the invention provides a method of producing nucheliolide derivative of formula (II), comprising: reacting materials to obtain the target compound of formula (II),

wherein the materials are nucheliolide and dimethylamine.

[0012] Specifically, the invention provides a method of producing a compound of formula (V), comprising:

dissolving material in CH2CI2, wherein the material is a compound of formula (II);

adjusting the pH to 4-5 by using of hydrochloric acid;

lyophilizing the aqueous solution to obtain the compound of formula (V).

[0013] The invention also provides a usage of the compound or salt thereof of formula (I) for curing a cancer, wherein, the cancer includes leukemia, breast cancer, prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0014] The invention also provides a compound of formula (I) or a salt thereof for use in the auxiliary treatment of cancer, wherein, the cancer includes leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0015] The invention also provides a compound of formula (I) or a salt thereof for use in a drug, wherein, the drug is used for cancer medical treatment, and the cancer includes leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0016] The invention also provides a compound of formula (I) or a salt thereof for use in a drug, wherein, the drug is used for cancer auxiliary medical treatment, and the cancer includes leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0017] The invention also provides a pharmaceutical composition for use in a method of treatment of cancer, comprising an effective amount of micheliolide derivatives of formula (I) or a or salt thereof of formula (I), in combination with a pharmaceutically acceptable carrier or other anti-cancer drug.

[0018] The invention also provides a compound of formula (II) or (V) or a salt thereof for use in the treatment of cancer, wherein, the cancer includes to leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0019] The invention also provides a compound of formula (II) or (V) or a salt thereof for use in the auxiliary treatment of cancer, wherein, the cancer includes leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0020] The invention also provides a compound of formula (II), (V) or a salt thereof for use in a drug, wherein, the drug is used for cancer medical treatment, and the cancer includes leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0021] The invention also provides a compound of formula (II), (V) or a salt thereof for use in a drug, wherein, the drug is used for cancer auxiliary medical treatment, and the cancer includes leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, 

melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0022] The invention also provides a pharmaceutical composition for use in a method of treatment of cancer, comprising an effective amount of micheliolide derivatives or salt thereof of formula (II), (V), in combination with a pharmaceutically acceptable carrier or other anti-cancer drug. The compounds in the embodiments of the present invention can be used directly or in the form of pharmaceutical composition as drug. The pharmaceutical compositions contain 0.1-99%, preferred 0.5-90% compounds of the present invention, and others are pharmaceutically acceptable pharmaceutical carrier and/or excipient which are harmless to animal and human or composition with other anti-cancer drug. Compositions in the embodiments of the present invention may be formulated as injection, tablet, and capsule.

[0023] The pharmaceutical carrier and excipient are a kind or many kinds of solid, semi-solid or liquid thinner and adjuvant drug. The dosage of pharmaceutical composition of the present invention may be based on unit weight. The compounds of the invention can be administrated by injection and oral form. The injection includes intravenous injection and intramuscular injection, and the oral form may be tablets and capsules.

[0024] Micheliolide derivatives or salt thereof in the embodiments of the present invention show good effect on cancer treatment, and no obvious inhibition to normal cells.

DETAILED DESCRIPTION OF THE INVENTION

[0025] The present invention is further described in detail hereinafter with reference to the accompanying drawings as well as embodiments so as to make the objective, technical scheme and merits thereof more apparent.

[0026] A compound, which is also micheliolide derivatives, provided in an embodiment of the present invention, is presented by

Rl is H or -C(O)R4, R4 is hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, aryl, alkyaryl, arylakyl, arylalkenyl, arylalkynyl and heterocyclic;

R3 is hydrogen, R2 is substituted alkyl having in the range of 1 up to 8 carbon atoms, where substituent is -NR/Rg;

where R7 and Rg are selected from hydrogen, alkyl having in the range of 1 up to 8 carbon atoms, or cycloalkyl;

Xis O;

Y is any of single bond, O, R^N and R12R13C, wherein, R-|-| is any of hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, aryl, alkyaryl, arylakyl, arylalkenyl, arylalkynyl or heterocyclic;

R-I2 and R13 are the same or different, they are any of hydrogen, fluorine, chlorine, bromine, iodine, alkyl, cycloalkyl, alkyl substituted by hydroxyl,alkenyl, alkynyl, aryl, heterocyclic, arylakyl, arylalkenyl, arylalkynyl, cyanomethyl, alkoxy or aryloxyalkyl respectively.

[0027] In an embodiment of the present invention, the substituent of the alkyl with Cpg comprises quaternary ammonium salts formed by -NR/Rg with RgZ;

Wherein, Z is any of fluorine, chlorine, bromine, iodine, tosylate, methanesulfonate, benzenesulfonate, and trifluoromethanesulfonate; Rg is any of alkyl, cycloalkyl, alkyl substituted by hydroxyl,alkenyl, alkynyl, aryl, heterocyclic, arylakyl, arylalkenyl, arylalkynyl, cyanomethyl, alkoxy or aryloxyalkyl; inorganic or organic acid are hydrofluoric acid, hydrochloric acid, 

hydrobromic acid, hydriodic acid, sulfuric acid, nitric acid, phosphoric acid, carbonic acid, boric acid, selenious acid, phosphomolybdic acid, phosphorous acid, sulfurous acid, citric acid, maleic acid, D-malic acid, L-malicacid, DL-malic acid, L-lactic acid, D-lactic acid, DL-lactic acid, oxalic acid, methanesulfonic acid, valeric acid, oleic acid, lauric acid, para-toluenesulfonic acid, 1-naphthalensulfonic acid, 2-naphthalensulfonic acid, phthalic acid, tartaric acid, malonic acid, succinic acid, fumaric acid, glycolic acid, thioglycolic acid, glycine, sarcocine, sulfonic acid, nicotinic acid, picolinic acid, isonicotinic acid, benzoic acid and substituted benzoic acid.

[0028] In an embodiment of the present invention, R2 is methylene substituted by -NRyRg, wherein, R7 and Rg are any of hydrogen, alkyl with 1 to 8 carbon atoms, any cycloalkyl respectively.

[0029] In an embodiment of the present invention, formula (I) is represented by formula (II)

[0030] In an embodiment of the present invention, formula (I) is represented by formula (V)

O              (V)

[0031] In an embodiment of the present invention, the compound disclosed above can be used in a drug, wherein the drug is used for cancer medical treatment, and the cancer comprises leukemia, breast cancer, prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0032] In an embodiment of the present invention, the compound disclosed above can be in a drug, wherein the drug is used for cancer auxiliary medical treatment, and the cancer comprises leukemia, breast cancer, Prostate cancer, nasopharyngeal carcinoma, colorectal cancer, lung cancer, liver cancer, esophageal carcinoma, gastric cancer, intestinal cancer, renal carcinoma, oral cavity cancer, Hodgkin lymphoma, pancreas cancer, colorectal cancer, cervical cancer, Non Hodgkin lymphoma, gliomas, melanoma, bladder carcinoma, ovarian cancer, thyroid carcinoma, sarcoma.

[0033] In an embodiment of the present invention, a pharmaceutical composition is provided for use in a method of treatment of cancer, comprising an effective amount of a compound described above, in combination with a pharmaceutically acceptable carrier or other anti-cancer drug.

[0034] In an embodiment of the present invention, a method producing a compound or salt thereof of formula (I) is provided, including: considering micheliolide as material, adding catalyst into organic solvent, and reacting the organic solvent with the catalyst and the material having the corresponding group or structure to obtain the target compound..

[0035] In an embodiment of the present invention, a method of producing nucheliolide derivative of formula (II) is provided, comprising: reacting materials to obtain the target compound of formula (II), wherein the materials are nucheliolide and dimethylamine.

[0036] In an embodiment of the present invention, a method of producing nucheliolide derivative of formula (V) is provided, comprising:

dissolving material in CH2CI2, wherein the material is a compound of formula (II);

adjusting the pH to 4-5 by using of hydrochloric acid;

lyophilizing the aqueous solution to obtain the compound of formula (V).

Embodiment 1

[0037] The producing of 11pH,13-Dihydro, 13-dimethylaminomicheliolide (compound II, which is represented by formula (II))

[0038] Micheliolide (106 mg, 0.40 mmol), triethylamine (2.0 mL), Me2NHHCI (41 mg, 0.5 mmol), and methanol (30 mL) are added to a 100-mL round flask. The resulting mixture is heated and refluxed for 3 hours, and then concentrated under reduced pressure to obtain crude residue which is purified by silica gel column chromatography (petroleum ether: ethyl acetate: triethylamine = 50:50:0.5) to obtain 107.4 mg white solid, wherein, the yield is 86%.

Formula: C17H27NO3

Molecular weight: 293

Properties: white amorphous powder

Spectra data:

[0039] 1H NMR (CDC13, 400 MHz) 5 3.76 (t, J = 10.0 Hz, 1H), 2.96 (s, 1H), 2.49-2.67 (m, 3H), 2.28-2.34 (m, 1H), 2.30-2.34 (m, 2H), 2.18 (s, 6H), 2.09 (br s, 2H), 1.96 (d, J = 11.2 Hz, 1H) 1.67-1.73 (m, 2H), 1.60 (s, 3H), 1.22 (br s, 3H), 1.18 (br s, 2H); 13C NMR (CDCI3, 300 MHz) 5 177.0, 131.8, 131.3, 84.0, 80.2, 58.3, 58.1, 50.9, 46.0, 44.6, 38.4, 35.3, 30.0, 27.2, 23.7, 22.8.

Reference embodiment 2

[0040] The producing of 4-propionylmicheliolide (Compound III, which is represented by formula (III))

(III)

[0041] Micheliolide (106 mg, 0.40 mmol), triethylamine (2.0 mL), propionylchloride (0.2 mL) and CH2CI2 (5 mL) are added to a 20-mL round flask. The resulting mixture is stirred for 3 hour at room temperature, and then concentrated under reduced pressure, and purified by using silica gel column chromatography (petroleum ether: ethyl acetate = 90:10), and finally 84 mg white solid are obtained. Wherein, the yield is 72%.

Formula: C18H24NO4

Molecular weight: 304

Properties: white amorphous powder

Spectra data:

[0042] 1H NMR (CDC13, 400 MHz) 5 6.14 (s, 1H), 5.42 (s, 1H), 3.74 (t, J = 10.0 Hz, 1H), 1.80-2.74 (m, 12H), 1.67 (s,3H), 1.50 (s, 3H), 1.07 (t, J = 4.0 Hz, 3H); 13C NMR (CDCI3, 300 MHz) 5 173.8, 170.1, 139.5, 131.5, 130.4, 118.6, 88.4, 83.0, 56.6, 50.1,36.5, 34.9, 30.4, 28.7, 25.9, 24.1, 18.8,9.1.

Reference embodiment 3

[0043] The producing of 1,10-Epoxymicheliolide (Compound IV, its structure was represented by formula (IV))

(IV)

[0044] Micheliolide (106 mg, 0.40 mmol), m-CPBA(2.0 mL), and CH2CI2 (5 mL) are added to a 20-mL round flask. The resulting mixture is stirred for 6 hours at the room temperature, and then concentrated under reduced pressure, purified by using silica gel column chromatography (petroleum ether: ethyl acetate = 80:20), and finally 96 mg white solid are obtained. Wherein, the yield is 91%.

Formula: C15H20NO4

Molecular weight: 264

Properties: white amorphous powder

Spectra data:

[0045] 1HNMR(CDCI3, 400 MHz) 5 6.13 (t, J = 3.2Hz, 1H), 5.44 (d, J = 2.8 Hz, 1H), 3.73 (t, J = 10.4 Hz, 1H), 1.30-2.46 (m, 11H), 1.29 (s, 3H), 1.28 (s, 3H); 13C NMR (CDCI3, 300 MHz) 5 168.7, 137.8, 118.6, 79.2, 77.3, 74.2, 66.7, 52.6, 48.4, 37.1,33.8, 29.0, 24.6, 22.5, 21.3.

[0046] Embodiment 4 The producing of 11pH,13-Dihydro, 13-dimethylaminomicheliolide hydrochloride (Compound V, its structure was represented by formula (V)) 

N—* HCI

O

compound II (293 mg, 1 mmol) is dissolved in CH2CI2 (2 mL) and was Stirred at room temperature, hydrochloric acid is added until pH = 4-5. The mixture was extracted with CH2CI2 (2x10 mL). The aqueous layer is lyophilized to obtain white solid, wherein, the yield is 82%. The structure data of the produced 11S, 11, 13-Dihydro, 13-dimethylaminomicheliolide hydrochloride are as follows:

Formula: C17H28CINO3

Molecular weight: 328.5

Properties: White amorphous powder

Spectra data:

[0047]

[a]D20 = -42.0 (c = 10, H2O); IR (KBr): 3334, 2927, 2856, 1767, 1467, 992, 967, 874, 831, 719, 669, 626, 504 cm’1; 1H NMR (D2O, 400 MHz) 54.1 (t, J= 10.3 Hz, 1H), 3.51 (q , J= 12.6 Hz, 1H), 3.40 (dd , J= 13.3, 2.9 Hz, 1H), 3.18-3.04 (m, 1H), 2.96 (d , J = 10.6 Hz, 6H), 2.67 (d , J= 10.2 Hz, 1H), 2.37 (dd , J= 16.2, 8.1 Hz, 1H), 2.27-2.05 (m, 4H), 1.87 (d , J= 12.9 Hz, 1H), 1.73 (dd , J = 19.5, 11.7 Hz, 2H), 1.66 (s, 3H), 1.46-1.31 (m, 2H), 1.26 (s, 3H); 13C NMR (CDCI3, 100 MHz) 5 178.4, 132.6, 131.4, 85.1, 80.7, 56.9, 55.6, 49.9, 45.1,42.3, 41.5, 39.2, 34.4, 29.5, 25.9, 23.2, 21.4.

Embodiment 5 The pharmacological of micheliolide derivatives

[0048] A variety of cancer cells are suspended to 2x105/mL, and then added into 24-hole Round-bottomed tissue culture plate. After that micheliolide and its derivatives are added, herein a test with one density occupies 5 holes. The resulting suspension are incubated (under 37 °C, 5% CO2) for 18 hours to allow the compounds to take effect. A absorbance (A) value is measured by using the method of MTT assay and an enzyme-linked detector under 570 nm wavelength, and then the inhibitory activity of the compounds is concluded. The result of the inhibitory activity is shown in Table 1.

Tablel. The inhibitory activity of micheliolide and its derivatives against different cancer cells (IC50, pM)

(Compound III and Compound IV are reference compounds)

Cell lines Compound II Compound III Compound IV Compound V

HL-60 2.4 4.5 5.8 11.5

K562 4.2 6.7 9.7 21.4

MCF-7 4.6 3.4 8.9 26.8

CNE-1 11.2 5.9 6.7 22.5

CNE-2 16.5 12.4 5.6 16.9

SW620 5.8 5.6 3.8 13.5

A549 7.2 7.7 5.7 18.1

HepG-2 4.5 15.4 7.4 27.9

Ec9706 9.2 7.6 6.6 15.7

SGC7901 14.6 14.7 13.4 24.9

SW1116 11.5 21.5 11.7 31.2

A498 12.4 5.3 4.3 16.3

ASPC-1 3.9 15.1 26.4 33.6

HT-29 4.8 9.8 9.8 19.2

HeLa 9.4 17.3 9.7 33.4

GL15 12.6 14.3 21.5 25.8

B16F1 3.4 13.2 5.2 18.6

T24 14.2 13.6 7.9 22.5

SKOV3 5.9 9.4 10.4 15.4

SW579 17.3 22.5 12.4 32.6

PC-3 8.7 11.4 17.2 23.5



[0049] In Table 1, HL-60, K562, MCF-7, CNE-1, CNE-2, SW620, A549, HepG2, Ec9706, SGC7901, SW1116, A498, ASPC-1, HT-29, HeLa, GL15, B16F1, T24, SKOV3, SW579, PC-3, represents acute leukemia cell lines, Chronic leukemia cell lines, Breast cancer cell lines, High differentiation nasopharyngeal carcinoma cell line, Poorly differentiated nasopharyngeal carcinoma cell lines, Colorectal cancer cell line, Lung cancer cell lines, Hepatocellular carcinoma cell lines, Esophageal cancer cell line, Gastric cancer cell line, Colon cancer cell line, Renal cell carcinoma cell line, Pancreatic cancer cell line, Colon cancer cell lines, uterine cervical cancer cell lines, Neuroblastoma cell lines, Melanoma cell line, human bladder cancer cell line, ovarian cancer cell lines, thyroid cancer cells, prostate cancer cell lines, respectively.

[0050] The tested result shows the compounds show strong inhibitory activity against the tested cells, however, have no obvious inhibition against normal cells at 50 pM.

Embodiment 6 Injection

[0051] Compounds II, III, IV, V produced in the embodiments 1 to 4, is respectively dissolved in a small amount of DMSO. Injective water is then added into the mixed solvent and filtered finely, after potting and sterilization, Finally the injection is obtained.

Embodiment 7 Tablet

[0052] The compounds II, III, IV, V produced in the embodiments 1 to 4, is mixed respectively with excipients according to weight ratio of 5:1, and then tableted to obtain tablets.

Embodiment 8 Capsule

[0053] The compounds II, III, IV, V prepared in the Examples 1-4, is mixed respectively with excipients according to weight ratio of 5:1 to obtain capsules.

[0054] The compounds, usage and producing methods of the present invention have been described with specific embodiments. It is obviously for those skilled in the art to appropriately change raw materials, process conditions et al, to achieve corresponding purposes.

REFERENCES CITED IN THE DESCRIPTION

This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

Non-patent literature cited in the description

. J. Nat. Prod., 1993, vol. 56, 90-98 [0005]

• Bioorg. Med. Chem. Lett., 2003, vol. 11, 1503-1510 [0005]