38
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4996 |
Atosiban
阿托西班,RWJ22164,RW22164 |
Oxytocin Receptor; Vasopressin Receptor | Endocrinology/Hormones; GPCR/G Protein |
Atosiban (RW22164) 是一种脱氨基催产素类似物,是一种九肽,也是竞争性的催产素受体拮抗剂。它是一种宫缩抑制剂,可用于自发早产的研究。 | |||
T11857 |
LIT-001
|
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
LIT-001 是非肽类催产素受体激动剂,EC50为55 nM,Ki 为226 nM。它可改善孤独症小鼠模型的社交互动。 | |||
T5148 |
Atosiban acetate
RW22164,Atosiban acetate (90779-69-4 free base),RWJ22164,醋酸阿托西班 |
Oxytocin Receptor; Vasopressin Receptor | Endocrinology/Hormones; GPCR/G Protein |
Atosiban acetate (RW22164) 是一种脱氨基催产素类似物,是一种九肽,也是竞争性的催产素受体拮抗剂。它是一种宫缩抑制剂,可用于自发早产的研究。 | |||
T12331L |
OT-R antagonist 1
Oxytocin receptor antagonist 1 |
Others | Others |
OT-R antagonist 1 inhibits oxytocin-evoked intracellular Ca2+ mobilization (IC50 = 8 nM). OT-R antagonist 1 is a new effective and selective nonpeptide low molecular weight OT-R antagonist. | |||
T12331 |
OT-R antagonist 2
Oxytocin receptor antagonist 2 |
Others | Others |
OT-R antagonist 2 is a nonpeptide low molecular weight antagonist of OT-R . | |||
T7601L |
Carbetocin acetate
醋酸卡贝缩宫素,Carbetocin acetate(37025-55-1 free base),卡贝缩宫素醋酸盐 |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
Carbetocin acetate 是催产素类似物,是催产素受体激动剂,Ki 是 7.1 nM。它对催产素受体的嵌合 N 末端具有高亲和力,Ki 为 1.17 μM。它能透过血脑屏障,可以通过激活 CNS 中的催产素受体而具有类抗抑郁活性,具有用于产后出血的研究潜力。 | |||
T7601 |
Carbetocin
卡贝缩宫素,醋酸卡贝缩宫素 |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
Carbetocin 是催产素类似物,是催产素受体激动剂,Ki 是 7.1 nM。它对催产素受体的嵌合 N 末端具有高亲和力,Ki 为 1.17 μM。它能透过血脑屏障,可以通过激活 CNS 中的催产素受体而具有类抗抑郁活性,具有用于产后出血的研究潜力。 | |||
T21534L |
Oxytocin C-terminal tripeptide Acetate
Oxytocin C-terminal tripeptide Acetate(2002-44-0 Free base) |
Others | Others |
Oxytocin C-terminal tripeptide Acetate 是 Oxytocin 的 C-末端三肽。Oxytocin 是哺乳动物的神经垂体激素,催产素受体的配体。 | |||
T3347 |
PF3274167
PF 3274167,Cligosiban,PF-3274167 |
OX Receptor | GPCR/G Protein; Neuroscience |
PF3274167 (Cligosiban) 是一种有效的、选择性的、高亲和力的非肽催产素受体拮抗剂。 | |||
T28855 |
SSR126768A
SSR-126768A,SSR 126768A |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
SSR126768A 是一种新型且具有选择性、口服活性和有效性的催产素(OT)受体拮抗剂,对子宫收缩有抑制作用,可用于预防早产。 | |||
T15682 |
L-371,257
|
Oxytocin Receptor; Vasopressin Receptor | Endocrinology/Hormones; GPCR/G Protein |
L-371,257 是催产素受体的竞争性拮抗剂,pA2 为 8.4,Ki 为 19 nM。 L-371,257 对加压素受体 1a 的 Ki 值为 3.7 nM。 | |||
TP2082L |
d[Cha4]-AVP acetate(500170-27-4 free base)
|
Vasopressin Receptor | GPCR/G Protein |
d[Cha4]-AVP acetate(500170-27-4 free base) 是一种有效的选择性人血管加压素 V1B 受体激动剂(V1B、V1A、催产素和 V2 受体的 Ki 值分别为 1.2、151、240 和 750 nM)。刺激 ACTH 和皮质酮分泌,并在体内表现出微不足道的血管加压活性。 | |||
T23441 |
TC OT 39
|
Others | Others |
oxytocin receptor partial agonist | |||
T23528 | WAY-267464 | Others | Others |
oxytocin receptor (OTR) agonist | |||
T11502 |
Epelsiban
GSK 557296 |
Others | Others |
Epelsiban is a selective and orally bioavailable oxytocin receptor antagonist (pKi: 9.9 for human oxytocin receptor). | |||
T28018 |
Merotocin
FE202767,FE 202767,FE-202767 |
||
Merotocin is a potent and highly selective peptidic agonist of the oxytocin receptor. | |||
T69504 |
Barusiban
|
||
Barusiban is an oxytocin receptor antagonist. | |||
T24292 |
L 366948
L366,948,L-366948,L-366,948,L 366,948,L366948 |
||
L 366948 is an antagonist of the oxytocin receptor. | |||
T25902 |
Ota-vasotocin
OVTA |
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Ota-vasotocin is a ligand utilized in quantitative receptor autoradiography for oxytocin receptors. | |||
T26602 |
ALS-I-41
|
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ALS-I-41 is a novel, potent and selective antagonist of oxytocin receptor. | |||
T12904 | SHR1653 | Others | Others |
SHR1653 is a highly potent, selective and brain penetrated antagonist of oxytocin receptor (OTR)(IC50 of 15 nM for hOTR). | |||
T80140 |
(Val3,Pro8)-Oxytocin
|
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
"(Val3,Pro8)-Oxytocin"为Gq依赖性途径的激动剂,同时作为β-arrestin结合及催产素受体(OXTR)内化作用的次级激动剂。 | |||
T79172 |
PF-06655075
|
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
PF-06655075为一新型非脑渗透性OT受体(oxytocin receptor)激动剂,具有显著提高对OT受体(oxytocin receptor)的选择性和药代动力学稳定性。PF-06655075可用作工具化合物,以研究外周OT在行为反应中的功能。 | |||
T11794 | L-368,899 hydrochloride | Others | Others |
L-368,899 hydrochloride, used as a tocolytic agent, is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist, with IC50s of 8.9 nM and 26 nM for rat uterus and human uterus oxytocin receptor, respectively. | |||
T31647 |
Epelsiban besylate
GSK-557296B,GSK557296B |
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Epelsiban Besylate is an oral drug that is a highly selective anamol oxytocin receptor antagonist. | |||
T76265 |
(Thr4,Gly7)-Oxytocin
|
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(Thr4,Gly7)-Oxytocin,一种Oxytocin类似物,特异性激活OT受体。通过激活TRPV1通道及抑制K+通道,诱导眼下神经元兴奋。 | |||
T80136 |
Val9-Oxytocin
|
Vasopressin Receptor | GPCR/G Protein |
Val9-Oxytocin为完全抗拮抗加压素(1a)受体的化合物,其结构上是Oxytocin的衍生物,特点在于Gly9位点被Val9取代。 | |||
T80126 |
(d(CH2)51,Tyr(Me)2,Orn8)-Oxytocin
|
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
'(d(CH2)51,Tyr(Me)2,Orn8)-Oxytocin (OVT)' 是催产素受体的一种拮抗剂,主要应用于神经系统疾病的研究领域。 | |||
T76590 |
(d(CH2)51,Tyr(Me)2,Thr4,Orn8,des-Gly-NH29)-Vasotocin
|
||
(d(CH2)51,Tyr(Me)2,Thr4,Orn8,des-Gly-NH29)-Vasotocin,是一种催产素受体拮抗剂,可消除 CA1 锥体神经元中催产素增强的抑制性突触后电流。 | |||
T81501 | PF-06655075 TFA | Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
PF-06655075(TFA)为PF-06655075的三氟乙酸(TFA)形态。该化合物是一种创新的非脑渗透性氧催产素(oxytocin receptor)受体激动剂,且对氧催产素受体具有较高的选择性,药代动力学稳定性得到显著增强。PF-06655075可用作工具化合物,以深入研究外围氧催产素受体在行为反应中的功能。 | |||
T70570 | Erlosiban | ||
Erlosiban, also known as OBE001, is a novel, orally active nonpeptide oxytocin receptor antagonist under development for the treatment of preterm labor and improvement in embryo implantation and pregnancy rate in assisted reproductive technology (ART). | |||
T24370 |
L-368899 free base
L 368899,L 368,899,L368,899,L-368899,L368899,L-368,899 |
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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). | |||
T11856 |
LIT-001 free base
|
Others | Others |
LIT-001 free base improves social interaction in a mouse model of autism. LIT-001 free base is the first nonpeptide oxytocin receptor (OT-R) agonist (EC50=55 nM; Ki=226 nM). | |||
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 negligible vasopressor activity in vivo. | |||
TP1927 |
d[Leu4,Lys8]-VP
|
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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. | |||
TP2136 |
(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin
|
||
Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and indu | |||
T79173 |
PF-06478939
|
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
PF-06478939为一种非脑渗透性肽类化合物,具有对催产素(OT)受体及加压素受体的激动效应,其EC50值分别为0.01 nM与0.078 nM。 | |||
T75933 |
d[Cha4]-AVP TFA
|
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d[Cha4]-AVP TFA 是一种有效的选择性加压素 (AVP)V1b 受体激动剂,对人V1b 受体的Ki 为 1.2 nM。d[Cha4]-AVP TFA 对 V1b 受体的选择性高于对人类 V1a 受体、V2 受体和催产素受体。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5145 |
Oxytocin acetate
Oxytocic hormone acetate,α-Hypophamine acetate,Oxytocin acetate (50-56-6 free base),醋酸催产素 |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
Oxytocin acetate (α-Hypophamine acetate) 是哺乳动物的神经垂体激素,是多效的下丘脑肽,是催产素受体的配体,有助于分娩、哺乳和亲社会行为。它可作为一种压力应对分子,具有抗炎、抗氧化剂和保护作用。 | |||
T5026 |
Oxytocin
催产素,α-Hypophamine,Oxytocic hormone,Oxytocin (Syntocinon) |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
Oxytocin (Oxytocin (Syntocinon)) 是哺乳动物的神经垂体激素,是多效的下丘脑肽,是催产素受体的配体,有助于分娩、哺乳和亲社会行为。它可作为一种压力应对分子,具有抗炎、抗氧化剂和保护作用。 |