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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T126501 | Xanthone V1a | ||
Xanthone V1a is a useful organic compound for research related to life sciences and the catalog number is T126501. | |||
T11857 | LIT-001 | Oxytocin Receptor | |
LIT-001 improves social interaction in a mouse model of autism.It is the first nonpeptide oxytocin receptor agonist with EC50 of 55 nM and Ki of 226 nM. | |||
T80160 | ω-Hexatoxin-Hv1a | ω-ACTX-Hv1,ω-Atracotoxin-HV1 | Calcium Channel |
ω-Hexatoxin-Hv1a, a neurotoxin extracted from the venom of the spider Hadronyche versuta, inhibits voltage-gated calcium channels [1] [2]. | |||
T6453 | Conivaptan hydrochloride | Vaprisol,Conivaptan HCl,YM 087 | Vasopressin Receptor |
Conivaptan hydrochloride (Vaprisol) is an orally active vasopressin V2 and V1A receptor antagonist, used in the therapy of hypervolemic hyponatremia and euvolemic. | |||
T4141 | RG7713 | RO 5028442 | Vasopressin Receptor |
RG7713 (RO 5028442) has been used in trials studying Autistic Disorder. | |||
TP2082L | D[Cha4]-AVP acetate(500170-27-4 free base) | Vasopressin Receptor | |
d[Cha4]-AVP acetate is a potent and selective human vasopressin V1B receptor agonist (Ki values are 1.2, 151, 240 and 750 nM for V1B, V1A, Oxytocin and V2 receptors respectively). Stimulates ACTH and corticosterone secre... | |||
T14494 | Balovaptan | RG7314 | Vasopressin Receptor |
Balovaptan (RG7314) is a highly potent and selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist, with Kis of 1 and 39 nM for human (hV1a) and mouse (mV1a) receptors. It is used for the research of autism. | |||
T16934 | SRX246 | Others | |
SRX246 has no interaction at V1b and V2 receptors. SRX246 shows negligible binding at 64 other receptors classes, including 35 G-proteincoupled receptors. SRX246 is a potent and CNS-penetrant vasopressin 1a (V1a) recepto... | |||
T17251 | VNA-932 | WAY-VNA 932 | Others |
VNA-932 is an agonist of the vasopressin V2-receptor (IC50: 80.3 nM and 778 nM in human-V2 binding and V1a binding assay). | |||
T15682 | L-371,257 | Oxytocin Receptor , Vasopressin Receptor | |
L-371,257 is a competitive antagonist of oxytocin receptor with pA2 of 8.4 and Ki of 19 nM. L-371,257 shows a Ki of 3.7 nM for vasopressin receptor 1a. | |||
T23393 | SR 49059 | Others | |
vasopressin V1A receptor antagonist | |||
T24625 | PF-184563 | PF184563,PF 184563 | |
PF-184563 is an effective and selective non-peptidic V1a receptor antagonist. | |||
T28745 | Selepressin | FE 202158,FE202158 | |
Selepressin, an analog of vasopressin, is a potent, selective vasopressin V1a receptor agonist. | |||
T28629 | RWJ 676070 | RWJ676070,RWJ-676070 | |
RWJ 676070 is an antagonist of vasopressin V1A/V2 receptor. | |||
T28854 | SRX 251 | SRX-251,SRX251 | |
SRX 251, a vasopressin V1a receptor antagonist, is used potentially for the treatment of primary dysmenorrhea. | |||
T29177 | YM 218 | YM218,YM-218 | |
YM 218 is a novel, potent, selective antagonist of nonpeptide vasopressin V1A receptor. | |||
T25577 | Khusimol | ||
Khusimol is a vasopressin V1a receptors non-peptide ligand that acts by inhibiting the binding of vasopressin. | |||
T29178 | YM 471 | YM-471,YM471 | |
YM 471 is a non-peptide arginine vasopressin (AVP) V1A and V2 receptor antagonist with oral activity. | |||
T80137 | (d(CH2)51,Tyr(Me)2,Dab5,Arg8)-Vasopressin | d(CH2)5[Tyr(Me)2, Dab5]AVP | Vasopressin Receptor |
(d(CH2)5[Tyr(Me)2, Dab5]AVP), a vasopressin V1a receptor-specific antagonist, demonstrates a pA2 value of 6.71 [1]. | |||
T24370 | L-368899 free base | L 368899,L 368,899,L368,899,L-368899,L368899,L-368,899 | |
L-368899 is a non-peptide and orally active antagonist of oxytocin receptor (IC50: 8.9 nM). It displays 40-fold selectivity over vasopressin V1a and V2 receptors (IC50: 370 and 570 nM respectively). |