Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T10735 | Target Info | |||
Target Name | Histidine decarboxylase (HDC) | ||||
Synonyms |
Human histidine decarboxylase
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Target Type | Clinical trial Target | ||||
Gene Name | HDC | ||||
Biochemical Class | Carbon-carbon lyase | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Vasopressin V2 receptor (V2R) | Successful Target | ||||
UniProt ID | V2R_HUMAN | |||||
Gene Name | AVPR2 | |||||
Synonyms |
Renal-type arginine vasopressin receptor; DIR3; DIR; Antidiuretic hormone receptor; AVPR V2; ADHR
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Representative Drug(s) | Lixivaptan | Drug Info | IC50 = 1 nM | [1] | ||
Co-Target Name | Vasopressin V1a receptor (V1AR) | Successful Target | ||||
UniProt ID | V1AR_HUMAN | |||||
Gene Name | AVPR1A | |||||
Synonyms |
Vascular/hepatic-type arginine vasopressin receptor; V1aR; V1a vasopressin receptor; Antidiuretic hormone receptor 1a; AVPR1; AVPR V1a
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Representative Drug(s) | Lixivaptan | Drug Info | Ki = 44 nM | [2] | ||
Co-Target Name | Oxytocin receptor (OTR) | Successful Target | ||||
UniProt ID | OXYR_HUMAN | |||||
Gene Name | OXTR | |||||
Synonyms |
OT-R
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Representative Drug(s) | Lixivaptan | Drug Info | IC50 = 519 nM | [3] |
References | Top | ||||
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REF 1 | (4-Substituted-phenyl)-(5H-10,11-dihydro-pyrrolo [2,1-c][1,4] benzodiazepin-10-yl)-methanone derivatives as vasopressin receptor modulators. Bioorg Med Chem Lett. 2005 Nov 15;15(22):5003-6. | ||||
REF 2 | Potent nonpeptide vasopressin receptor antagonists based on oxazino- and thiazinobenzodiazepine templates. Bioorg Med Chem Lett. 2004 Jun 7;14(11):2747-52. | ||||
REF 3 | Identification and synthesis of major metabolites of Vasopressin V2-receptor agonist WAY-151932, and antagonist, Lixivaptan. Bioorg Med Chem Lett. 2007 Nov 1;17(21):5796-800. |
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