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  1. General Info
  2. Effects Info
  3. Reference
Drug Details
01. General Information
Name Disulfiram
PubChem CID 3117
Molecular Weight 296.5g/mol
Synonyms

disulfiram, Tetraethylthiuram disulfide, 97-77-8, Antabuse, Bis(diethylthiocarbamoyl) disulfide, Antabus, Alcophobin, Anticol, Esperal, Teturam, TETD, Dicupral, Exhorran, Hoca, Ethyldithiurame, Abstensil, Antaethyl, Antietanol, Antivitium, Contralin, Tetradine, Tetraetil, Teturamin, Abstinil, Abstinyl, Antadix, Antalcol, Antetan, Antetil, Antietil, Antikol, Aversan, Averzan, Cronetal, Krotenal, Refusal, Etabus, Ethyl tuads, Ethyl Thiram, Ethyl Thiurad, Ethyl Tuex, Antaenyl, Antaetil, Antiaethan, Contrapot, Disulfan, Disulfuram, Ephorran, Stopetyl, Thiuranide, Anteyl, Bonibal, Disetil, Nocbin, Tenurid, Tenutex, Tetidis, Ekagom TEDS, Ekagom TETDS, Ethyldithiourame, Noxal, Anti-ethyl, Alk-aubs, Tetraethylthiuram disulphide, Thiuram E, TATD, Soxinol TET, Tetraethylthiram disulfide, Ekagom DTET, Accel TET, Espenal, Exhoran, Sanceler TET-G, Ro-sulfiram, Tetraethylthioperoxydicarbonic diamide, Tetraethylthiuram, Tuads, ethyl, Usaf B-33, Sanceler TET, Stopaethyl, Thireranide, Antaethan, Antethyl, Tetradin, Tillram, Accel TET-R, Ethyl Thiudad, Dupon 4472, Tetraethylthiuran disulfide, Anthethyl, Disulphuram, Dupont fungicide 4472, Hocakrotenalnci-C02959, Tetraethylthiram disulphide, Bis(diethylthiocarbamyl) disulfide, Tetraethylthiuram sulfide, Thiuram disulfide, tetraethyl-, N,N,N',N'-Tetraethylthiuram disulfide, Antabuse (TN), Bis(N,N-diethylthiocarbamoyl) disulfide, 1,1'-Dithiobis(N,N-diethylthioformamide), Disulfide, bis(diethylthiocarbamoyl), ENT 27,340, Thioperoxydicarbonic diamide, tetraethyl-, Bis(diethylthiocarbamoyl)disulphide, NCI-C02959, diethylcarbamothioylsulfanyl N,N-diethylcarbamodithioate, NSC-25953, N,N-diethyl[(diethylcarbamothioyl)disulfanyl]carbothioamide, NSC 190940, Bis(N,N-diethylthiocarbamoyl)disulphide, N,N,N',N'-Tetraethylthiuram disulphide, Bis((diethylamino)thioxomethyl)disulphide, Bis((diethylamino)thioxomethyl) disulfide, Tetraethylthiuram disulfide;TETD, TTS, TR3MLJ1UAI, MFCD00009048, Thioperoxydicarbonic diamide ([(H2N)C(S)]2S2), tetraethyl-, CHEMBL964, MLS000069818, CHEBI:4659, ORA102, DTXSID1021322, ORA-102, NSC25953, Esperal [France], CAS-97-77-8, NCGC00016000-08, NCGC00016000-13, SMR000059171, Thioperoxydicarbonic diamide (((H2N)C(S))2S2), tetraethyl-, 1,1',1'',1'''-[disulfanediylbis(carbonothioylnitrilo)]tetraethane, Ancazide ET, Akrochem TETD, Perkacit TETD, Ekaland TETD, Perkait TETD, Ethyl Tuads Rodform, C10H20N2S4, DTXCID101322, Disulfiramum [INN-Latin], Disulfiramo [INN-Spanish], Bis[(diethylamino)thioxomethyl] disulfide, CCRIS 582, 1,1'-Dithiobis[N,N-diethylthioformamide], HSDB 3317, SR-01000076145, UNII-TR3MLJ1UAI, EINECS 202-607-8, NSC 25953, AI3-27340, Formamide, 1,1'-dithiobis(N,N-diethylthio-, Thioperoxydicarbonic diamide (((H2N)C(S))2S2), N,N,N',N'-tetraethyl-, Thioperoxydicarbonic diamide ([(H2N)C(S)]2S2), N,N,N',N'-tetraethyl-, Disulfiram [USP:INN:BAN:JAN], Bis(diethylthiocarbamyoyl)disulfide, Prestwick_182, Disulfiram (Antabuse), Spectrum_001010, CPD000059171, Disulfiram (Antabuse)?, DISULFIRAM [MI], Opera_ID_224, DISULFIRAM [INN], DISULFIRAM [JAN], Prestwick0_000097, Prestwick1_000097, Prestwick2_000097, Prestwick3_000097, Spectrum2_001176, Spectrum3_000405, Spectrum4_000228, Spectrum5_001590, DISULFIRAM [HSDB], DISULFIRAM [IARC], Lopac-T-1132, 1,N-diethylthioformamide], DISULFIRAM [VANDF], Formamide, 1,1'-dithiobis(N,N-diethylthio)-, UPCMLD-DP090, EC 202-607-8, T 1132, tetraethyl thiuram disulfide, DISULFIRAM [MART.], Tetraethyldithiuram disulfide, DISULFIRAM [WHO-DD], Lopac0_001164, SCHEMBL27213, BSPBio_000054, BSPBio_001930, KBioGR_000895, KBioSS_001490, MLS000758264, MLS001076475, MLS001423963, SPECTRUM1500262, SPBio_001191, SPBio_001993, BPBio1_000060, Disulfiram (JP17/USP/INN), GTPL7168, DISULFIRAM [EP IMPURITY], DISULFIRAM [ORANGE BOOK], UPCMLD-DP090:001, KBio2_001490, KBio2_004058, KBio2_006626, KBio3_001150, DISULFIRAM [EP MONOGRAPH], Thioperoxydicarbonic diamide ((H2N)C(S))2S2, tetraethyl-, DISULFIRAM [USP MONOGRAPH], HMS1568C16, HMS1920I16, HMS2051M17, HMS2090C18, HMS2091O22, HMS2095C16, HMS2230K06, HMS3263J09, HMS3371B21, HMS3393M17, HMS3655I19, HMS3712C16, HMS3867H13, Pharmakon1600-01500262, BCP07331, HY-B0240, bis-(diethyl-thiocarbamyl)-disulfide, Tox21_110280, Tox21_300403, Tox21_400072, Tox21_501164, BDBM50058655, CCG-39549, DL-379, HB1119, N,N',N'-Tetraethylthiuram disulfide, NSC756748, NSC800739, s1680, STL069539, 1,1',1'',1'''-{disulfanediylbis[(thioxomethylene)-nitrilo]}tetraethane, AKOS000120201, Tox21_110280_1, AT13284, DB00822, HS-0057, LP01164, NC00063, NSC-756748, NSC-800739, SDCCGSBI-0051131.P005, WLN: 2N2 & YUS & S 2, NCGC00016000-01, NCGC00016000-02, NCGC00016000-03, NCGC00016000-04, NCGC00016000-05, NCGC00016000-06, NCGC00016000-07, NCGC00016000-09, NCGC00016000-10, NCGC00016000-11, NCGC00016000-12, NCGC00016000-14, NCGC00016000-15, NCGC00016000-18, NCGC00016000-29, NCGC00094423-01, NCGC00094423-02, NCGC00094423-03, NCGC00094423-05, NCGC00094423-06, NCGC00094423-07, NCGC00254447-01, NCGC00261849-01, N,N,N'',N''-tetraethylthiuram disulfide, BIS(DIETHYLTHIOCARBAMOYL) DISULPHIDE, Formamide,1'-dithiobis(N,N-diethylthio)-, SBI-0051131.P004, 1,1''-dithiobis(N,N-diethylthioformamide), DB-057683, AB00051976, B0479, EU-0101164, FT-0631502, FT-0667720, NS00010096, SW196492-4, Tetraethylthiuram disulfide, >=97.0% (S), EN300-19458, C01692, D00131, S00294, AB00051976-20, AB00051976-21, AB00051976-23, AB00051976_22, AB00051976_25, A845750, Q409665, Q-201812, SR-01000076145-1, SR-01000076145-5, SR-01000076145-8, BRD-K32744045-001-05-6, BRD-K32744045-001-17-1, Z104473910, Disulfiram, British Pharmacopoeia (BP) Reference Standard, Disulfiram, European Pharmacopoeia (EP) Reference Standard, Disulfiram, United States Pharmacopeia (USP) Reference Standard, 1,1'',1'''',1''''''-[disulfanediylbis(carbonothioylnitrilo)]tetraethane, Disulfiram, Pharmaceutical Secondary Standard; Certified Reference Material, N,N-diethylcarbamodithioic acid [[diethylamino(sulfanylidene)methyl]thio] ester, THIOPEROXYDICARBONIC DIAMIDE ((H2N)C(S))(SUB 2) S(SUB 2), TETRAETHYL-, InChI=1/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H, TETRAETHYLTHIOPEROXYDICARBONIC DIAMIDE ((((C(SUB 2)H(SUB 5))(SUB 2)N)C(S))(SUB 2)S(SUB 2))

Drug Type Small molecule
Formula C₁₀H₂₀N₂S₄
SMILES CCN(CC)C(=S)SSC(=S)N(CC)CC
InChI 1S/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H3
InChIKey AUZONCFQVSMFAP-UHFFFAOYSA-N
CAS Number 97-77-8
ChEMBL ID CHEMBL964
ChEBI ID CHEBI:4659
TTD ID D0X5SD
Drug Bank ID DB00822
KEGG ID C01692
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
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2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Enhancing Drug Efficacy
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Combination Pair ID: 387
Pair Name Curcumin, Disulfiram
Partner Name Curcumin
Disease Info [ICD-11: 2C30] Melanoma Investigative
Biological Phenomena Induction-->Oxidative stress
In Vitro Model B16-F10 Mouse melanoma Mus musculus (Mouse) CVCL_0159
In Vivo Model Tumor cells (2×10⁶ cells per 500 μL) were implanted subcutaneously into the left hind groin of mice. The compounds were dissolved in 5% DMSO and provided to the mice intraperitoneally once a day for 15 consecutive days.
Result Combination Therapy of Curcumin and Disulfiram Synergistically Inhibits the Growth of B16-F10 Melanoma Cells by Inducing Oxidative Stress
03. Reference
No. Title Href
1 Combination Therapy of Curcumin and Disulfiram Synergistically Inhibits the Growth of B16-F10 Melanoma Cells by Inducing Oxidative Stress. Biomolecules. 2022 Oct 31;12(11):1600. doi: 10.3390/biom12111600. Click
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