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Cat No. | Product Name | Synonyms | Targets |
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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. | |||
T5148 | Atosiban acetate | RW22164,Atosiban acetate (90779-69-4 free base),RWJ22164 | Oxytocin Receptor , Vasopressin Receptor |
Atosiban acetate (RW22164) is an inhibitor of the hormones oxytocin and vasopressin. It is used as an intravenous medication as a labour repressant (tocolytic) to halt premature labor. Atosiban acetate (RW22164) inhibits... | |||
T12331 | OT-R antagonist 2 | Oxytocin receptor antagonist 2 | Others |
OT-R antagonist 2 is a nonpeptide low molecular weight antagonist of OT-R . | |||
T12331L | OT-R antagonist 1 | Oxytocin receptor antagonist 1 | 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. | |||
T4996 | Atosiban | RWJ22164,RW22164 | Oxytocin Receptor , Vasopressin Receptor |
Atosiban (RW22164) is an inhibitor of the hormones oxytocin and vasopressin. It is used as an intravenous medication as a labour repressant (tocolytic) to halt premature labor. Atosiban inhibits the oxytocin-mediated rel... | |||
T7601L | Carbetocin acetate | Carbetocin acetate(37025-55-1 free base) | Oxytocin Receptor |
Carbetocin acetate is an obstetric drug used to control postpartum hemorrhage and bleeding after giving birth. | |||
T7601 | Carbetocin | Oxytocin Receptor | |
Carbetocin is an obstetric drug used to control postpartum hemorrhage and bleeding after giving birth. | |||
T21534L | Oxytocin C-terminal tripeptide Acetate | Oxytocin C-terminal tripeptide Acetate(2002-44-0 Free base) | Others |
Oxytocin C-terminal tripeptide Acetate is the C-terminal tripeptide of Oxytocin.Oxytocin is a mammalian neuropituitary hormone, a ligand for the oxytocin receptor. | |||
T3347 | PF3274167 | PF 3274167,Cligosiban,PF-3274167 | OX Receptor |
PF3274167 (Cligosiban) is a potent and selective, high-affinity nonpeptide oxytocin receptor antagonist. | |||
T28855 | SSR126768A | SSR-126768A,SSR 126768A | Oxytocin Receptor |
SSR126768A is a novel and selective, orally active and potent oxytocin (OT) receptor antagonist with inhibitory effects on uterine contractions for the prevention of preterm labor. | |||
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. | |||
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... | |||
T23528 | WAY-267464 | Others | |
oxytocin receptor (OTR) agonist | |||
T23441 | TC OT 39 | Others | |
oxytocin receptor partial agonist | |||
T11502 | Epelsiban | GSK 557296 | Others |
Epelsiban is a selective and orally bioavailable oxytocin receptor antagonist (pKi: 9.9 for human oxytocin receptor). | |||
T69504 | Barusiban | ||
Barusiban is an oxytocin receptor antagonist. | |||
T25902 | Ota-vasotocin | OVTA | |
Ota-vasotocin is a ligand utilized in quantitative receptor autoradiography for oxytocin receptors. | |||
T31647 | Epelsiban besylate | GSK-557296B,GSK557296B | |
Epelsiban Besylate is an oral drug that is a highly selective anamol 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. | |||
T79172 | PF-06655075 | Oxytocin Receptor | |
PF-06655075 is a novel, non-brain-penetrant oxytocin receptor agonist that demonstrates enhanced selectivity for the oxytocin receptor and substantially improved pharmacokinetic stability. This compound serves as a tool ... | |||
T11794 | L-368,899 hydrochloride | 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,... | |||
T12904 | SHR1653 | Others | |
SHR1653 is a highly potent, selective and brain penetrated antagonist of oxytocin receptor (OTR)(IC50 of 15 nM for hOTR). | |||
T26602 | ALS-I-41 | ||
ALS-I-41 is a novel, potent and selective antagonist of oxytocin receptor. | |||
T28018 | Merotocin | FE202767,FE 202767,FE-202767 | |
Merotocin is a potent and highly selective peptidic agonist of the oxytocin receptor. | |||
T80140 | (Val3,Pro8)-Oxytocin | Oxytocin Receptor | |
(Val3,Pro8)-Oxytocin functions primarily as a Gq-dependent pathway agonist and exhibits secondary activity as a reduced efficacy agonist for β-arrestin recruitment and receptor-mediated endocytosis at the oxytocin recept... | |||
T76265 | (Thr4,Gly7)-Oxytocin | ||
(Thr4,Gly7)-Oxytocin, an analogue of Oxytocin and a specific OT receptor agonist, not only activates TRPV1 channels to excite subicular neurons but also reduces the activity of potassium (K+) channels. [1] [2]. | |||
T80136 | Val9-Oxytocin | Vasopressin Receptor | |
Val9-Oxytocin, an Oxytocin analog where Gly9 is substituted with Val9 [1], functions as a complete antagonist of the vasopressin (V1a) receptor. | |||
T80126 | (d(CH2)51,Tyr(Me)2,Orn8)-Oxytocin | Oxytocin Receptor | |
(d(CH2)51,Tyr(Me)2, Orn8)-Oxytocin (OVT) is an antagonist of the oxytocin receptor that finds application in the study of neurological diseases [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). | |||
T81501 | PF-06655075 TFA | Oxytocin Receptor | |
PF-06655075 (TFA) is the trifluoroacetic acid (TFA) salt of PF-06655075, a novel, non-brain-penetrant oxytocin receptor agonist that exhibits enhanced selectivity for the oxytocin receptor and improved pharmacokinetic st... | |||
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, serving as an oxytocin receptor antagonist, effectively nullifies the augmentation of inhibitory postsynaptic currents in CA1 pyramidal neurons by oxytocin [1]. | |||
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 assiste... | |||
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. | |||
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... | |||
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 prolonge... | |||
T11856 | LIT-001 free base | 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). | |||
T79173 | PF-06478939 | Oxytocin Receptor | |
PF-06478939 is a peptide that functions as an agonist at the oxytocin (OT) receptor and vasopressin receptor without crossing the blood-brain barrier. It exhibits EC50 values of 0.01 nM at the OT receptor and 0.078 nM at... | |||
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... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T5145 | Oxytocin acetate | Oxytocic hormone acetate,α-Hypophamine acetate,Oxytocin acetate (50-56-6 free base) | Oxytocin Receptor |
Oxytocin acetate (α-Hypophamine acetate) is a mammalian neurohypophysial hormone, a ligand of oxytocin receptor. | |||
T5026 | Oxytocin | α-Hypophamine,Oxytocic hormone,Oxytocin (Syntocinon) | Oxytocin Receptor |
Oxytocin (Oxytocin (Syntocinon)) is a mammalian neurohypophysial hormone, a ligand of oxytocin receptor. |
Cat No. | Product Name | Species | Expression System |
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TMPH-01820 | OXT Protein, Human, Recombinant (His) | Human | Yeast |
Neurophysin 1 specifically binds oxytocin.; Oxytocin causes contraction of the smooth muscle of the uterus and of the mammary gland. Acts by binding to oxytocin receptor (OXTR). | |||
TMPH-01821 | OXT Protein, Human, Recombinant (His & Myc & SUMO) | Human | E. coli |
Neurophysin 1 specifically binds oxytocin.; Oxytocin causes contraction of the smooth muscle of the uterus and of the mammary gland. Acts by binding to oxytocin receptor (OXTR). | |||
TMPH-00279 | Interferon tau-1/IFNT1 Protein, Bovine, Recombinant (His) | Bovine | Yeast |
Paracrine hormone primarily responsible for maternal recognition of pregnancy. Interacts with endometrial receptors, probably type I interferon receptors, and blocks estrogen receptor expression, preventing the estrogen-... | |||
TMPH-00278 | Interferon tau-1/IFNT1 Protein, Bovine, Recombinant (E. coli, His) | Bovine | E. coli |
Paracrine hormone primarily responsible for maternal recognition of pregnancy. Interacts with endometrial receptors, probably type I interferon receptors, and blocks estrogen receptor expression, preventing the estrogen-... | |||
TMPH-01794 | NR2F6 Protein, Human, Recombinant (His & Myc) | Human | HEK293 |
Transcription factor predominantly involved in transcriptional repression. Binds to promoter/enhancer response elements that contain the imperfect 5'-AGGTCA-3' direct or inverted repeats with various spacings which are a... | |||
TMPH-01795 | NR2F6 Protein, Human, Recombinant (His & SUMO) | Human | E. coli |
Transcription factor predominantly involved in transcriptional repression. Binds to promoter/enhancer response elements that contain the imperfect 5'-AGGTCA-3' direct or inverted repeats with various spacings which are a... |