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Search Results for " vasopressin-v2 "

20

Compounds

Cat No. Product Name Synonyms Targets
T6288 Mozavaptan OPC31260l,OPC-31260 Vasopressin Receptor
Mozavaptan (OPC-31260) is a competitive vasopressin receptor antagonist for both V1 and V2 receptors with IC50 of 1.2 μM and 14 nM, respectively.
T64174 Vasopressin V2 receptor antagonist 1
Vasopressin V2 receptor antagonist 1 (Compound 4g) is a vasopressin V2receptor (V2R) antagonist (Ki: 3.8 nM). dominant polycystic kidney disease (ADPKD).
T7303 LIXIVAPTAN VPA-985,WAY-VPA 985 Vasopressin Receptor
Lixivaptan (VPA-985) is an orally active and selective vasopressin receptor V2 antagonist(Ki = 2.3 nM)
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.
T15273 Fedovapagon VA483,A106483 Vasopressin Receptor
Fedovapagon (VA106483) is a selective and potent agonist of the vasopressin V2 receptor (V2R) that inhibits the growth of intersegmental vessels in zebrafish. Fedovapagon can be used to study overactive bladder, nocturia...
T5144 Desmopressin acetate (16679-58-6 free base) Desmopressin acetate,DDAVP Vasopressin Receptor
Desmopressin acetate (16679-58-6 free base) (DDAVP) is the synthetic analog of the antidiuretic hormone arginine vasopressin. Vasopressin Receptor The antidiuretic properties of desmopressin have led to its use in polyur...
T2326 Tolvaptan OPC-41061 Vasopressin Receptor , Autophagy
Tolvaptan (OPC-41061) is an orally bioavailable, selective, arginine vasopressin receptor 2 (V2, AVPR2) antagonist that can be used to treat hyponatremia.
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...
T28629 RWJ 676070 RWJ676070,RWJ-676070
RWJ 676070 is an antagonist of vasopressin V1A/V2 receptor.
T29178 YM 471 YM-471,YM471
YM 471 is a non-peptide arginine vasopressin (AVP) V1A and V2 receptor antagonist with oral activity.
T24759 Satavaptan fumarate SR-121463A,SR 121463 A,SR-121463 A,SR121463A
Satavaptan fumarate is a selective antagonist of the non-peptide vasopressin V2 receptor.
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).
T27965 M-0002 RWJ-351647,SPD556,SPD-556,M0002,RWJ351647
M-0002, a vasopressin V2 receptor antagonist, is used potentially for the treatment of ascites.
T28664 Satavaptan SR121463,SR 121463,SR-121463
Satavaptan is a vasopressin V2 receptor antagonist. Satavaptan improves the control of ascites in cirrhosis.
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).
T62906 Lazuvapagon
Lazuvapagon is a vasopressin V2 receptor agonist that can be used to study enuresis.
TP2082 D[Cha4]-AVP
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 secretion and exhibits negligi...
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...
TP1927 D[Leu4,Lys8]-VP
Selective vasopressin V1B receptor agonist (Ki values are 0.16, 64, 100 and 3800 nM for V1B, oxytocin, V2 and V1A receptors respectively). Displays weak antidiuretic, vasopressor and in vitro oxytocic activities.
T75933 D[Cha4]-AVP TFA
d[Cha4]-AVP TFA is a potent and selective agonist for the vasopressin (AVP) V1b receptor, displaying a high affinity with a K i of 1.2 nM. It exhibits greater selectivity for the V1b receptor over the V1a receptor, V2 re...
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