Target Validation Information | |||||
---|---|---|---|---|---|
TTD ID | T52790 | ||||
Target Name | Substance-K receptor (TACR2) | ||||
Type of Target |
Clinical trial |
||||
Drug Potency against Target | CS-003 | Drug Info | Ki = 0.54 nM | [10] | |
DNK-333 | Drug Info | Ki = 5.5 nM | [7] | ||
Saredutant | Drug Info | Ki = 0.5 nM | [8] | ||
4-(4-butylpiperidin-1-yl)-1-o-tolylbutan-1-one | Drug Info | Ki < 1000 nM | [6] | ||
A-987306 | Drug Info | IC50 = 5.7 nM | [3] | ||
Hoo-Phe-Orn-Pro-hle-Pff-Phe-NH2 | Drug Info | IC50 = 710 nM | [2] | ||
L-732138 | Drug Info | Ki = 134 nM | [5] | ||
PMX-53 | Drug Info | IC50 = 87 nM | [2] | ||
Rambazole | Drug Info | Ki = 16 nM | [1] | ||
WAY-207024 | Drug Info | Ki = 330 nM | [4] | ||
Action against Disease Model | DNK-333 | Drug Info | Male Brown Norway rats were imaged prior to and 10, 30 and 60 min after intra-tracheal challenge with capsaicin (30 microg kg(-1)) or vehicle (0.5% ethanol solution). Capsazepine (3.5 mg kg(-1)), DNK333 (10 mg kg(-1)) but not DSCG (10 mg kg(-1)) administered prophylactically were able to block the effect of capsaicin in the airways | [9] | |
References | |||||
REF 1 | Generation of a new class of hNK(2) receptor ligands using the 'fragment approach'. Bioorg Med Chem Lett. 2005 Feb 1;15(3):585-8. | ||||
REF 2 | Peptidomimetic C5a receptor antagonists with hydrophobic substitutions at the C-terminus: increased receptor specificity and in vivo activity. Bioorg Med Chem Lett. 2006 Oct 1;16(19):5088-92. | ||||
REF 3 | cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11a-octahydrobenzofuro[2,3-h]quinazolin-2-amine (A-987306), a new histamine H4R antagonist that blocks pain... J Med Chem. 2008 Nov 27;51(22):7094-8. | ||||
REF 4 | Discovery of 6-({4-[2-(4-tert-butylphenyl)-1H-benzimidazol-4-yl]piperazin-1-yl}methyl)quinoxaline (WAY-207024): an orally active antagonist of the ... J Med Chem. 2009 Apr 9;52(7):2148-52. | ||||
REF 5 | Biological and conformational evaluation of bifunctional compounds for opioid receptor agonists and neurokinin 1 receptor antagonists possessing tw... J Med Chem. 2010 Aug 12;53(15):5491-501. | ||||
REF 6 | Discovery of N-{1-[3-(3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-yl)propyl]piperidin-4-yl}-2-phenylacetamide (Lu AE51090): an allosteric muscarinic M1 rec... J Med Chem. 2010 Sep 9;53(17):6386-97. | ||||
REF 7 | Dual neurokinin NK(1)/NK(2) antagonists: N-[(R,R)-(E)-1-arylmethyl-3-(2-oxo-azepan-3-yl)carbamoyl]allyl-N-methyl-3,5-bis(trifluoromethyl)benzamides and 3-[N'-3,5-bis(trifluoromethyl)benzoyl-N-arylmethyl-N'-methylhydrazino]-N-[(R)-2-oxo-azepan-3-yl]propionamides. Bioorg Med Chem Lett. 2001 Dec 3;11(23):3081-4. | ||||
REF 8 | Recent developments in the medicinal chemistry of NK2 receptor antagonists. Curr Top Med Chem. 2003;3(12):1436-45. | ||||
REF 9 | Capsaicin-induced mucus secretion in rat airways assessed in vivo and non-invasively by magnetic resonance imaging. Br J Pharmacol. 2007 Apr;150(8):1022-30. | ||||
REF 10 | Novel triple neurokinin receptor antagonist CS-003 strongly inhibits neurokinin related responses. Eur J Pharmacol. 2008 May 31;586(1-3):306-12. | ||||
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