Drug Information
Drug General Information | Top | |||
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Drug ID |
D0E0LQ
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Former ID |
DAP000318
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Drug Name |
Thiothixene
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Synonyms |
Navan; Navane; Navaron; Orbinamon; Thiothixine; Tiotixene; Tiotixeno; Tiotixenum; Thiothixene hydrochloride; P 4657B; CP 12252-1; Cis-Thiothixene; Navane (TN); P-4657 B; P-4657A; P-4657B; Thiothixene (USP); Thiothixene (Z); Thiothixene Hydrochloride (base); Thiothixene [USAN:BAN]; Tiotixene (JAN); Tiotixeno [INN-Spanish]; Tiotixenum [INN-Latin]; Trans-Thiothixene; P-4657-B; CP-12,252-1; CP-12,252-1 base; {2-(Dimethylsulfamoyl)-[9-(4-methyl-1-piperazinyl)propylidene]thiox} anthene; N,N-Dimethyl-9-[3-(4-methyl-1-piperazinyl)propylidene]thiaxanthene-2-sulfonamide; N,N-Dimethyl-9-[3-(4-methyl-1-piperazinyl)propylidene]thioxanthene-2-sulfonamide; N,N-dimethyl-9-[3-(4-methylpiperazin-1-yl)propylidene]thioxanthene-2-sulfonamide; N,N-Dimethyl-9-(3-(4-methyl-1-piperazinyl)propylidene)thioxanthene-2-sulfonamide; Trans-N,N-Dimethyl-9-(3-(4-methyl-piperazinyl)propylidene)thioxanthene-2-sulfonamide; Cis-N,N-Dimethyl-9-(3-(4-methyl-1-piperazinyl)propylidene)thioxanthene-2-sulfonamide; N,N-Dimethyl-9-(3-(4-methylpiperazin-1-yl)propylidene)-9H-thioxanthene-2-sulphonamide; (9E)-N,N-dimethyl-9-[3-(4-methylpiperazin-1-yl)propylidene]-9H-thioxanthene-2-sulfonamide; (9E)-N,N-dimethyl-9-[3-(4-methylpiperazin-1-yl)propylidene]thioxanthene-2-sulfonamide; (9Z)-N,N-dimethyl-9-[3-(4-methylpiperazin-1-yl)propylidene]thioxanthene-2-sulfonamide; (E)-Thiothixene; 2-(Dimethylsulfamoyl)-(9-(4-methyl-1-piperazinyl)propylidene)thioxanthene
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Drug Type |
Small molecular drug
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Indication | Schizophrenia [ICD-11: 6A20] | Approved | [1], [2] | |
Therapeutic Class |
Antipsychotic Agents
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Company |
Pfizer Pharmaceuticals
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Structure |
Download2D MOL |
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Formula |
C23H29N3O2S2
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Canonical SMILES |
CN1CCN(CC1)CCC=C2C3=CC=CC=C3SC4=C2C=C(C=C4)S(=O)(=O)N(C)C
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InChI |
1S/C23H29N3O2S2/c1-24(2)30(27,28)18-10-11-23-21(17-18)19(20-7-4-5-9-22(20)29-23)8-6-12-26-15-13-25(3)14-16-26/h4-5,7-11,17H,6,12-16H2,1-3H3/b19-8-
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InChIKey |
GFBKORZTTCHDGY-UWVJOHFNSA-N
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CAS Number |
CAS 3313-26-6
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PubChem Compound ID | ||||
PubChem Substance ID |
616474, 7847440, 7980778, 9208389, 10527275, 11532885, 12013417, 14759539, 44891823, 46505564, 47217055, 47736752, 47811025, 48035404, 48110727, 48334780, 50054592, 50054593, 50111253, 57408892, 76674035, 81049375, 93167171, 103358973, 110097312, 124750269, 124799400, 126673294, 134221874, 134337630, 135022512, 135651260, 137005727, 140637626, 151990180, 160964859, 175268220, 179148852, 184580899, 184590634, 223667992, 223704321, 226420796, 241073624, 241180615, 249983475, 252347478, 252401248, 252451220, 252655323
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ChEBI ID |
CHEBI:9571
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ADReCS Drug ID | BADD_D02204 | |||
SuperDrug ATC ID |
N05AF04
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SuperDrug CAS ID |
cas=003313266
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Interaction between the Drug and Microbe | Top | |||
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The Metabolism of Drug Affected by Studied Microbe(s) | ||||
The Order in the Taxonomic Hierarchy of the following Microbe(s): Eubacteriales | ||||
Studied Microbe: Blautia hansenii DSM20583
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[3] | |||
Hierarchy | ||||
Experimental Method | High-throughput screening | |||
Description | Thiothixene can be metabolized by Blautia hansenii DSM20583 (log2FC = -0.577; p = 0.043). | |||
Studied Microbe: Clostridium sp.
Show/Hide Hierarchy
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[3] | |||
Hierarchy | ||||
Experimental Method | High-throughput screening | |||
Description | Thiothixene can be metabolized by Clostridium sp. (log2FC = -0.594; p = 0.003). |
References | Top | |||
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REF 1 | URL: 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: 212). | |||
REF 2 | FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (ANDA) 070600. | |||
REF 3 | Mapping human microbiome drug metabolism by gut bacteria and their genes. Nature. 2019 Jun;570(7762):462-467. | |||
REF 4 | Dopaminergic stimulation of cAMP accumulation in cultured rat mesangial cells. Am J Physiol. 1987 Aug;253(2 Pt 2):H358-64. |
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