Dacarbazine (BioDeep_00000000370)
Secondary id: BioDeep_00001867494
human metabolite blood metabolite Chemicals and Drugs Volatile Flavor Compounds
代谢物信息卡片
化学式: C6H10N6O (182.09160500000002)
中文名称: 达卡巴嗪
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 6.45%
分子结构信息
SMILES: CN(C)N/N=C\1/C(=NC=N1)C(=O)N
InChI: InChI=1S/C6H10N6O/c1-12(2)11-10-6-4(5(7)13)8-3-9-6/h3H,1-2H3,(H2,7,13)(H,8,9)
描述信息
Dacarbazine appears as white to ivory microcrystals or off-white crystalline solid. (NTP, 1992)
(E)-dacarbazine is a dacarbazine in which the N=N double bond adopts a trans-configuration.
An antineoplastic agent. It has significant activity against melanomas. (from Martindale, The Extra Pharmacopoeia, 31st ed, p564). Dacarbazine with Oblimersen is in clinical trials for the treatment of malignant melanoma.
Dacarbazine is an Alkylating Drug. The mechanism of action of dacarbazine is as an Alkylating Activity.
Dacarbazine (also known as DTIC) is an intravenously administered alkylating agent used in the therapy of Hodgkin disease and malignant melanoma. Dacarbazine therapy has been associated with serum enzyme elevations during therapy and occasional cases of severe and distinctive acute hepatic failure, probably caused by acute sinusoidal obstruction syndrome.
Dacarbazine is a triazene derivative with antineoplastic activity. Dacarbazine alkylates and cross-links DNA during all phases of the cell cycle, resulting in disruption of DNA function, cell cycle arrest, and apoptosis. (NCI04)
An antineoplastic agent. It has significant activity against melanomas. (from Martindale, The Extra Pharmacopoeia, 31st ed, p564)
Dacarbazine is only found in individuals that have used or taken this drug. It is an antineoplastic agent. It has significant activity against melanomas. (from Martindale, The Extra Pharmacopoeia, 31st ed, p564)The mechanism of action is not known, but appears to exert cytotoxic effects via its action as an alkylating agent. Other theories include DNA synthesis inhibition by its action as a purine analog, and interaction with SH groups. Dacarbazine is not cell cycle-phase specific.
L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01A - Alkylating agents
C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent
D009676 - Noxae > D000477 - Alkylating Agents
D000970 - Antineoplastic Agents
同义名列表
124 个代谢物同义名
Dacarbazine, Pharmaceutical Secondary Standard; Certified Reference Material; Imidazole-4(or 5)-carboxamide, 5(or 4)-(3,3-dimethyl-1-triazeno)-; Dacarbazine, United States Pharmacopeia (USP) Reference Standard; 4-(or 5)-(3,3-Dimethyl-1-triazeno)imidazole-5(or 4)-carboxamide; 4-[(1E)-3,3-Dimethyltriaz-1-en-1-yl]-1H-imidazole-5-carboxamide; (5E)-5-(dimethylaminohydrazinylidene)imidazole-4-carboxamide; (5E)-5-(dimethylaminohydrazinylidene)-4-imidazolecarboxamide; Dacarbazine, European Pharmacopoeia (EP) Reference Standard; 5-[(1E)-dimethyltriaz-1-en-1-yl]-1H-imidazole-4-carboxamide; 1 H-IMIDAZOLE-4-CARBOXAMIDE, 5-(3,3-DIMETHYL-1-TRIAZENYL)-; Dacarbazine, British Pharmacopoeia (BP) Reference Standard; 5-(3,3-dimethyltriaz-1-en-1-yl)-1H-imidazole-4-carboxamide; 1H-imidazole-4-carboxamide, 5-(3,3-dimethyl-1-triazenyl)-; 4-(5)-(3,3-Dimethyl-1-triazeno)imidazole-5(4)-carboxamide; 4(5)-(3,3-Dimethyl-1-triazeno)imidazole-5(4)-carboxamide; 4-[(E)-dimethylaminodiazenyl]-1H-imidazole-5-carboxamide; 5-(3,3-Dimethyltriaz-1-enyl)-1H-imidazole-4-carboxamide; 5-(3,3-Dimethyl-1-triazenyl)-1H-imidazole-4-carboxamide; 5(or 4)-(dimethyltriazeno)imidazole-4(or 5)-carboxamide; 5-(3-3-dimethyl-1-triazenyl)-1H-imidazole-4-carboxamide; 5-(dimethyltriaz-1-en-1-yl)-1H-imidazole-4-carboxamide; (5Z)-5-(dimethylaminohydrazono)imidazole-4-carboxamide; (5E)-5-(dimethylaminohydrazono)imidazole-4-carboxamide; Imidazole-4-carboxamide, 5-(3,3-dimethyl-1-triazenyl)-; 5- (3,3-Dimethyl-1-triazenyl) imidazole-4-carboxamide; 4(5)-(3,3-Dimethyl-1-triazeno)imidazole-4-carboxamide; IMIDAZOLE-4-CARBOXAMIDE, 5-(3,3-DIMETHYL-1-TRIAZENO1-; Imidazole-4(or 5)-carboxamide,3-dimethyl-1-triazeno)-; Imidazole-4-carboxamide, 5-(3,3-dimethyl-1-triazeno)-; Carboxamide, 5-(3,3-dimethyl-1-triazeno)imidazole-4-; 5-(3,3-Dimethyl-1-triazenyl)imidazole-4-carboxamide; 4-[(E)-dimethylaminoazo]-1H-imidazole-5-carboxamide; 1H-Imidazole-4-carboxamide,3-dimethyl-1-triazenyl)-; 4-(3,3-Dimethyl-1-triazeno)imidazole-5-carboxamide; 5-(3,3-Dimethyl-1-triazeno)imidazole-4-carboxamide; 5-(3,3-Dimethyltriazeno)imidazole-4-carboxamide; Imidazole-4-carboxamide,3-dimethyl-1-triazeno)-; Carboxamide,3-dimethyl-1-triazeno)imidazole-4-; 5-(Dimethyltriazeno)imidazole-4-carboxamide; 5-(Dimethyltriazeno)imidazole-4-carboximide; 4-(Dimethyltriazeno)imidazole-5-carboxamide; Dimethyl (triazeno) imidazolecarboxamide; Dimethyl-triazeno-imidazole-carboximide; Dimethyl Triazeno Imidazole Carboxamide; dimethyl-triazeno-imidazole carboxamide; Imidazole Carboxamide Dimethyltriazeno; (Dimethyltriazeno)imidazolecarboxamide; Dimethyl Triazeno Imidazol Carboxamide; Dimethyltriazenoimidazolecarboxamide; Dacarbazine [USAN:USP:INN:BAN:JAN]; Di-me-triazenoimidazolecarboxamide; Carboxamide, Dimethyl Imidazole; Imidazole Carboxamide, Dimethyl; Dimethyl Imidazole Carboxamide; DACARBAZINE [USP MONOGRAPH]; DACARBAZINUM [WHO-IP LATIN]; DACARBAZINE (USP MONOGRAPH); FDKXTQMXEQVLRF-ZHACJKMWSA-N; DACARBAZINE [EP MONOGRAPH]; DACARBAZINE (EP MONOGRAPH); DACARBAZINE [ORANGE BOOK]; Dacarbazine (JAN/USP/INN); Dacarbazino [INN-Spanish]; WLN: T5M CNJ DVZ ENUNN1&1; Dacarbazinum [INN-Latin]; Dacarbazine (DTIC-Dome); Imidazole carboxamide; DACARBAZINE [WHO-DD]; Dacarbazina Almirall; DACARBAZINE (USP-RS); DACARBAZINE [WHO-IP]; DACARBAZINE [USP-RS]; DACARBAZINE (MART.); DACARBAZINE [MART.]; DACARBAZINE [VANDF]; DACARBAZINE [USAN]; DACARBAZINE [IARC]; DACARBAZINE [HSDB]; dacarbazine - dtic; DACARBAZINE (IARC); DACARBAZINE [JAN]; DACARBAZINE [INN]; Dacarbazine-DTIC; DACARBAZINE [MI]; (E)-Dacarbazine; UNII-7GR28W0FJI; Tox21_111171_1; Biocarbazine R; Dtic-Dome (TN); Dacarbazinum; Tox21_111171; Biocarbazine; Tox21_201010; Dacarbazine; Dacarbasine; dacarbazina; Dacarbazino; Dicarbazine; Decarbazine; Dakarbazin; NCI-C04717; Dacarbazin; 7GR28W0FJI; NSC-45388; Fauldetic; AI3-52825; DTIC-Dome; Detimedac; DTIC Dome; dtic-aome; HSDB 3219; NSC 45388; Deticene; DTICDome; L01AX04; Asercit; Dacatic; ICDMT; DTIE; DTCI; DTIC; ICDT; DIC; Dacarbazine
数据库引用编号
25 个数据库交叉引用编号
- ChEBI: CHEBI:177836
- ChEBI: CHEBI:94587
- ChEBI: CHEBI:4305
- KEGG: C06936
- KEGGdrug: D00288
- PubChem: 135398738
- PubChem: 5351166
- PubChem: 2942
- HMDB: HMDB0014989
- Metlin: METLIN540
- DrugBank: DB00851
- ChEMBL: CHEMBL1574179
- ChEMBL: CHEMBL476
- Wikipedia: Dacarbazine
- MeSH: Dacarbazine
- ChemIDplus: 0004342034
- chemspider: 10437816
- chemspider: 10481959
- CAS: 750512-03-9
- CAS: 4342-03-4
- CAS: 4342-3-4
- PMhub: MS000019412
- PubChem: 9152
- RefMet: Dacarbazine
- KNApSAcK: 4305
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
1 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Herwig Strik, Thomas Efferth, Bernd Kaina. Artesunate in glioblastoma therapy: Case reports and review of clinical studies.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
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Analytical chemistry.
2023 08; 95(31):11567-11571. doi:
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BMC complementary medicine and therapies.
2023 Apr; 23(1):111. doi:
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International journal of oncology.
2022 Sep; 61(3):. doi:
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Medicine.
2022 Jul; 101(28):e29354. doi:
10.1097/md.0000000000029354
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Acta bio-medica : Atenei Parmensis.
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Echocardiography (Mount Kisco, N.Y.).
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Thrombosis and haemostasis.
2022 04; 122(4):506-516. doi:
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Cell biology international.
2022 Jan; 46(1):73-82. doi:
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Shock (Augusta, Ga.).
2021 12; 56(6):1092-1093. doi:
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. [PMID: 33927139] - Hongxu Liu, William Kwame Amakye, Jiaoyan Ren. Codonopsis pilosula polysaccharide in synergy with dacarbazine inhibits mouse melanoma by repolarizing M2-like tumor-associated macrophages into M1-like tumor-associated macrophages.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2021 Oct; 142(?):112016. doi:
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BMJ case reports.
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Anti-cancer agents in medicinal chemistry.
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Molecular pharmacology.
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Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
2019 Mar; 125(?):549-561. doi:
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European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
2019 Mar; 136(?):156-163. doi:
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Biomaterials science.
2019 Feb; 7(3):1161-1178. doi:
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The British journal of radiology.
2018 Nov; 91(1091):20170172. doi:
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International journal of biological macromolecules.
2018 Sep; 116(?):1260-1267. doi:
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Journal of cancer research and clinical oncology.
2018 Aug; 144(8):1475-1485. doi:
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Oncology reports.
2018 Jun; 39(6):2855-2864. doi:
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Scientific reports.
2018 04; 8(1):6516. doi:
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Disease models & mechanisms.
2018 02; 11(2):. doi:
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Materials science & engineering. C, Materials for biological applications.
2018 Feb; 83(?):44-50. doi:
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International journal of molecular sciences.
2018 Jan; 19(2):. doi:
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Fluids and barriers of the CNS.
2018 Jan; 15(1):2. doi:
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Biochemical and biophysical research communications.
2018 01; 495(1):1292-1299. doi:
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International journal of oncology.
2018 Jan; 52(1):295-304. doi:
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International journal of nanomedicine.
2018; 13(?):3039-3051. doi:
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BioMed research international.
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Nihon Hinyokika Gakkai zasshi. The japanese journal of urology.
2018; 109(2):106-110. doi:
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Pediatric blood & cancer.
2018 Jan; 65(1):. doi:
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Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology.
2018; 49(6):2443-2462. doi:
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AJNR. American journal of neuroradiology.
2017 Dec; 38(12):2243-2250. doi:
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Molecular cancer therapeutics.
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Anticancer research.
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Leukemia research.
2017 11; 62(?):91-97. doi:
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Clinical cancer research : an official journal of the American Association for Cancer Research.
2017 Nov; 23(21):6441-6449. doi:
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Clinical cancer research : an official journal of the American Association for Cancer Research.
2017 Oct; 23(20):6215-6226. doi:
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International journal of STD & AIDS.
2017 10; 28(12):1259-1262. doi:
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British journal of cancer.
2017 Sep; 117(7):921-924. doi:
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Medical science monitor : international medical journal of experimental and clinical research.
2017 Aug; 23(?):4117-4125. doi:
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Neuro-oncology.
2017 Aug; 19(8):1097-1108. doi:
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Nutrition and cancer.
2017 Aug; 69(6):873-880. doi:
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Bioscience reports.
2017 Jun; 37(3):. doi:
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Analytica chimica acta.
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Cancer biology & therapy.
2017 06; 18(6):400-406. doi:
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Neuro-oncology.
2017 06; 19(6):845-852. doi:
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Veterinary and comparative oncology.
2017 Jun; 15(2):594-605. doi:
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Cell biology international.
2017 Jun; 41(6):680-690. doi:
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Archives of toxicology.
2017 06; 91(6):2493-2494. doi:
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Biomaterials science.
2017 May; 5(5):1041-1050. doi:
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Phytotherapy research : PTR.
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Journal of neuro-oncology.
2017 05; 132(3):401-407. doi:
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European journal of cancer (Oxford, England : 1990).
2017 05; 76(?):84-92. doi:
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Oncotarget.
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Neuro-oncology.
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Cancer immunology, immunotherapy : CII.
2017 Mar; 66(3):379-389. doi:
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Molecular medicine reports.
2017 Feb; 15(2):597-604. doi:
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Journal of nanoscience and nanotechnology.
2017 Feb; 17(2):977-82. doi:
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Bioconjugate chemistry.
2017 01; 28(1):194-202. doi:
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Oncotarget.
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Journal of neuro-oncology.
2017 01; 131(1):193-199. doi:
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Journal of immunology research.
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Molecular pharmaceutics.
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Drug delivery.
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Pakistan journal of pharmaceutical sciences.
2016 Nov; 29(6):2079-2082. doi:
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Bioorganic & medicinal chemistry letters.
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Drug delivery.
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Scientific reports.
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