Drug Information
Drug General Information | |||||
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Drug ID |
D02TJS
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Former ID |
DAP000768
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Drug Name |
Dicumarol
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Synonyms |
Acadyl; Acavyl; Anathrombase; Antitrombosin; Apekumarol; Baracoumin; Bishydroxycoumarin; Cuma; Cumid; Dicoumal; Dicoumarin; Dicoumarol; Dicoumarolum; Dicoumerol; Dicuman; Dicumarine; Dicumarinum; Dicumarolo; Dicumarolum; Dicumol; Dikumarol; Dufalone; Dwukumarol; Kumoran; Melitoxin; Temparin; Trombosan; Dicumaol R; Dicumarol [USAN]; Dicumarolo [DCIT]; Dwukumarol [Polish]; Uncoupler of oxidative respiration; M0216; NC 034; Bis-hydroxycoumarin; Dicoumarol (INN); Dicoumarolum [INN-Latin]; Dicumarol (TN); Dicumarol (USAN); Dicumarol [INN-Spanish]; Symmetric dicoumarol analogue, 1; Bis(4-hydroxycoumarin-3-yl)methane; Di-(4-hydroxy-3-coumarinyl)methane; Bis-3,3'-(4-hydroxycoumarinyl)methane; Bis-3,3'-(4-oxycoumarinyl)ethylacetate; Di-4-hydroxy-3,3'-methylenedicoumarin; Coumarin, 3,3'-methylenebis[4-hydroxy-(8CI); 2-hydroxy-3-[(2-hydroxy-4-oxochromen-3-yl)methyl]chromen-4-one; 2H-1-Benzopyran-2-one, 3,3'-methylenebis[4-hydroxy-(9CI); 3,3′-Methylenebis(4-hydroxycoumarin); 3,3'-Methyleen-bis(4-hydroxy-cumarine); 3,3'-Methyleen-bis(4-hydroxy-cumarine) [Dutch]; 3,3'-Methylen-bis(4-hydroxy-cumarin); 3,3'-Methylen-bis(4-hydroxy-cumarin) [German]; 3,3'-Methylene-bis(4-hydroxycoumarin); 3,3'-Methylene-bis(4-hydroxycoumarine); 3,3'-Methylene-bis(4-hydroxycoumarine) [French]; 3,3'-Methylenebis(4-hydroxy-1,2-benzopyrone); 3,3'-Methylenebis(4-hydroxy-2H-1-benzopyran-2-one); 3,3'-Methylenebis(4-hydroxycoumarin); 3,3'-Methylenebis[4-hydroxy-1,2-benzopyrone]; 3,3'-Methylenebis[4-hydroxy-2H-1-benzopyran-2-one]; 3,3'-Methylenebis[4-hydroxycoumarin]; 3,3'-Metilen-bis(4-idrossi-cumarina); 3,3'-Metilen-bis(4-idrossi-cumarina) [Italian]; 3,3'-methanediylbis(4-hydroxy-2H-chromen-2-one); 3,3'-methylenebis(2-hydroxy-4h-chromen-4-one); 3,3'-methylenebis(4-hydroxy-2H-chromen-2-one); 3,3-Methylene-bis[4-hydroxycoumarin]; 4,4'-Dihydroxy-3,3'-methylene bis coumarin
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Drug Type |
Small molecular drug
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Therapeutic Class |
Anticoagulants
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Structure |
Download2D MOL |
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Formula |
C19H12O6
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InChI |
InChI=1S/C19H12O6/c20-16-10-5-1-3-7-14(10)24-18(22)12(16)9-13-17(21)11-6-2-4-8-15(11)25-19(13)23/h1-8,20-21H,9H2
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InChIKey |
DOBMPNYZJYQDGZ-UHFFFAOYSA-N
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CAS Number |
CAS 66-76-2
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PubChem Compound ID | |||||
PubChem Substance ID |
2636, 4054, 81051, 96557, 606498, 828851, 841964, 3138564, 3288931, 5394319, 7979068, 8149297, 10321191, 10532227, 11112184, 11131943, 11220586, 11336071, 11361310, 11363059, 11365621, 11368183, 11371493, 11374194, 11376345, 11462282, 11466813, 11467933, 11483984, 11486565, 11487960, 11490203, 11492323, 11493979, 11532436, 14851261, 17397886, 24439015, 24896643, 26611698, 26680286, 26747987, 26747988, 26758600, 36502598, 46505536, 47216838, 47291197, 47440330, 47515376
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SuperDrug ATC ID |
B01AA01
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SuperDrug CAS ID |
cas=000066762
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Target and Pathway | |||||
Target(s) | Vitamin K epoxide reductase complex subunit 1 | Target Info | Inhibitor | [537681] | |
KEGG Pathway | Ubiquinone and other terpenoid-quinone biosynthesis | ||||
PathWhiz Pathway | Vitamin K Metabolism | ||||
Coagulation | |||||
References | |||||
Ref 541890 | (http://www.guidetopharmacology.org/) Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 6808). | ||||
Ref 550685 | Drug information of Dicumarol, 2008. eduDrugs. | ||||
Ref 551871 | Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015 |
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