General Information of DTT (ID: TTSCIUP)

DTT Name Oxytocin receptor (OTR) DTT Info
Gene Name OXTR

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Approved Drug(s)
Discontinued Drug(s)
Clinical Trial Drug(s)
Patented Agent(s)
Investigative Drug(s)
4 Approved Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Carbetocin DMUSLW3 Postpartum haemorrhage JA43 Approved [1]
Desmopressin DMS3GVE Diabetic complication 5A2Y Approved [2]
Oxytocin DMDL27I Autism spectrum disorder 6A02 Approved [3]
ATOSIBAN DMB7WYM N. A. N. A. Phase 4 [4]
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5 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Retosiban DMOYGZF Preterm labour JB00 Phase 3 [5]
Barusiban DMWI0X3 Androgen deficiency 5A81.1 Phase 2 [6]
FE-202767 DMDGZ1C Erectile dysfunction HA01.1 Phase 2 [3]
GSK-557296 DM3ZL2O Premature ejaculation HA03.0Z Phase 2 [7]
SSR149415 DMCMD93 Anxiety disorder 6B00-6B0Z Phase 2 [8]
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10 Patented Agent(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
PMID28906174-Compound-figure1g DMECU90 N. A. N. A. Patented [9]
Pyrrolidine derivative 10 DMCQN5M N. A. N. A. Patented [9]
Pyrrolidine derivative 11 DMIHRV9 N. A. N. A. Patented [9]
Pyrrolidine derivative 12 DMXO8R5 N. A. N. A. Patented [9]
Pyrrolidine derivative 13 DM3VA8P N. A. N. A. Patented [9]
Pyrrolidine derivative 9 DMZK658 N. A. N. A. Patented [9]
Triazole derivative 4 DMCFEAS N. A. N. A. Patented [9]
Triazole derivative 5 DMA83QK N. A. N. A. Patented [9]
Triazole derivative 6 DMU15FW N. A. N. A. Patented [9]
Triazole derivative 7 DMRK4AT N. A. N. A. Patented [9]
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⏷ Show the Full List of 10 Patented Agent(s)
5 Discontinued Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
L-368899 DM5LRKC Miscarriage JA00.0 Discontinued in Phase 1 [10]
PF-3274167 DMD42MN Female sexual arousal dysfunction HA01.1 Discontinued in Phase 1 [11]
TT-235 DMHJXL6 Miscarriage JA00.0 Discontinued in Phase 1 [12]
AS-602305 DMH78J6 Androgen deficiency 5A81.1 Terminated [13]
L-371257 DMCRQTH N. A. N. A. Terminated [11]
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66 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
1'-tosylspiro[indene-1,4'-piperidine] DM9SYEP Discovery agent N.A. Investigative [11]
ARGENINE VASOPRESSIN DM8KN0Q Discovery agent N.A. Investigative [14]
D(CH2)5[Tyr(Me)2,Thr4,Orn8(5/6C-Flu),Tyr-NH29]VT DMVHMGA Discovery agent N.A. Investigative [15]
D(CH2)5[Tyr(Me)2,Thr4,Orn8,Tyr9-NH2]VT DM1BMT7 Discovery agent N.A. Investigative [15]
d(CH2)5[Tyr(Me)2]AVP DMHTSAX Discovery agent N.A. Investigative [16]
DesGly-NH2,d(CH2)5[D-Tyr2,Thr4,Orn8(5/6C-Flu)]VT DMJK0H5 Discovery agent N.A. Investigative [15]
D[Arg4,Dab8]VP DMCU8HK Discovery agent N.A. Investigative [14]
D[Arg4,Lys8]VP DM69OVM Discovery agent N.A. Investigative [14]
D[Arg4,Orn8]VP DM8D4QT Discovery agent N.A. Investigative [14]
D[Arg4]AVP DM76Q2B Discovery agent N.A. Investigative [14]
D[Cha4,Dab8]VP DMCLUXI Discovery agent N.A. Investigative [14]
D[Cha4,Dap8]VP DMAPZKB Discovery agent N.A. Investigative [14]
D[Cha4,Lys8]VP DM0GO7U Discovery agent N.A. Investigative [14]
D[Cha4,Orn8]VP DMZWTJK Discovery agent N.A. Investigative [14]
D[Cha4]AVP DM8FCX5 Discovery agent N.A. Investigative [14]
D[Leu4,Dab8]VP DMNSXG9 Discovery agent N.A. Investigative [14]
D[Leu4,Dap8]VP DME3HK8 Discovery agent N.A. Investigative [14]
D[Leu4,Lys8]VP DMDBU7Q Discovery agent N.A. Investigative [14]
D[Leu4,Orn8]VP DMJCW8Y Discovery agent N.A. Investigative [14]
D[Leu4]AVP DMREZT7 Discovery agent N.A. Investigative [14]
D[Lys8(5/6-Flu)]VT DME2PKB Discovery agent N.A. Investigative [15]
D[Orn4,Lys8]VP DMNQTBU Discovery agent N.A. Investigative [14]
D[Orn4,Orn8]VP DMONV0M Discovery agent N.A. Investigative [14]
D[Orn4]AVP DMJNT95 Discovery agent N.A. Investigative [14]
D[Orn8(5/6C-Flu)]VT DMH791N Discovery agent N.A. Investigative [15]
D[Thr4,Lys8(5/6C-Flu)]VT DMS4F8O Discovery agent N.A. Investigative [15]
D[Thr4,Orn8(5/6C-Flu)]VT DMBDZQA Discovery agent N.A. Investigative [15]
D[Val4]AVP DM3GM8E Discovery agent N.A. Investigative [14]
L-365,209 DM1WMHO Discovery agent N.A. Investigative [16]
L-366,509 DMGQE1B Discovery agent N.A. Investigative [16]
L-366,682 DMAS5P8 Discovery agent N.A. Investigative [16]
L-366,948 DM31NXF Discovery agent N.A. Investigative [16]
L-367,773 DMQ369D Discovery agent N.A. Investigative [16]
L-372662 DMQV974 Discovery agent N.A. Investigative [11]
L023103 DM9KWUR Discovery agent N.A. Investigative [17]
LS-192629 DMUBF53 Discovery agent N.A. Investigative [18]
PF-271836 DMYSWAZ Female sexual arousal dysfunction HA01.1 Investigative [3]
PMID16250654C37 DMIT4UN Discovery agent N.A. Investigative [19]
SSR126768A DMF0X2S Discovery agent N.A. Investigative [20]
[35S]-non-peptide OT antagonist DMSHOQ8 Discovery agent N.A. Investigative [21]
[Aib7]OT DMUCAXT Discovery agent N.A. Investigative [22]
[D-Tic7]OT DME8W3R Discovery agent N.A. Investigative [22]
[Gly(But)7]OT DMZM3GB Discovery agent N.A. Investigative [22]
[HO1][Lys8(5/6C-Flu)]VT DMLZNK6 Discovery agent N.A. Investigative [15]
[HO1][Orn8(5/6C-Flu)]VT DMFK9V5 Discovery agent N.A. Investigative [15]
[HO1][Orn8(5/6C-Rhm)]VT DM7COAM Discovery agent N.A. Investigative [15]
[HO1][Thr4,Lys8(5/6C-Flu)]VT DMT2UYR Discovery agent N.A. Investigative [15]
[HO1][Thr4,Orn8(5/6C-Flu)]VT DM81B4W Discovery agent N.A. Investigative [15]
[L-Tic7]OT DMHUMDR Discovery agent N.A. Investigative [22]
[Lys8(Alexa 488) ]PVA DM7STF6 Discovery agent N.A. Investigative [23]
[Lys8(Alexa 546) ]PVA DM38L6U Discovery agent N.A. Investigative [23]
[Mpa1, D-Tic2, Aib7]OT DM27LNU Discovery agent N.A. Investigative [22]
[Mpa1, D-Tic7]OT DMPT1ME Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, Aib7, D-Tic9]OT DMBPVSD Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, Aib7]OT DMQSG6Y Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, D-Tic7, Aib9]OT DM5GSXC Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, D-Tic7, D-Tic9]OT DMI9MBO Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, D-Tic7]OT DM3T4JF Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, Gly(But)3, Gly(But)7]OT DML8V4F Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, Gly(But)7]OT DMX2SU9 Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, L-Tic7]OT DM0H3NV Discovery agent N.A. Investigative [22]
[Mpa1, D-Tyr(Et)2, Pip7]OT DM6W4LR Discovery agent N.A. Investigative [22]
[Mpa1, L-Tic7]OT DMB4J3N Discovery agent N.A. Investigative [22]
[Phe3]OT DMK18CS Discovery agent N.A. Investigative [24]
[Pip7]OT DMXJDEA Discovery agent N.A. Investigative [22]
[Thr4,Gly7]OT DM7QAKB Discovery agent N.A. Investigative [25]
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⏷ Show the Full List of 66 Investigative Drug(s)
Molecule Interaction Atlas

References

1 Peptide and non-peptide agonists and antagonists for the vasopressin and oxytocin V1a, V1b, V2 and OT receptors: research tools and potential therapeutic agents. Prog Brain Res. 2008;170:473-512.
2 Design of potent and selective agonists for the human vasopressin V1b receptor based on modifications of [deamino-cys1]arginine vasopressin at position 4. J Med Chem. 2004 Apr 22;47(9):2375-88.
3 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 369).
4 Pyridobenzodiazepines: a novel class of orally active, vasopressin V2 receptor selective agonists. Bioorg Med Chem Lett. 2006 Feb 15;16(4):954-9.
5 The Effect of an Oxytocin Receptor Antagonist (Retosiban, GSK221149A) on the Response of Human Myometrial Explants to Prolonged Mechanical Stretch.Endocrinology.2015 Oct;156(10):3511-6.
6 The effect of barusiban, a selective oxytocin antagonist, in threatened preterm labor at late gestational age: a randomized, double-blind, placebo-controlled trial. Am J Obstet Gynecol. 2009 Jun;200(6):627.e1-10.
7 Inhibition of ejaculation by the non-peptide oxytocin receptor antagonist GSK557296: a multi-level site of action. Br J Pharmacol. 2013 Aug;169(7):1477-85.
8 Tetrahydroquinoline sulfonamides as vasopressin 1b receptor antagonists. Bioorg Med Chem Lett. 2009 Nov 1;19(21):6018-22.
9 A patent review of oxytocin receptor antagonists 2013-2017.Expert Opin Ther Pat. 2017 Dec;27(12):1287-1290.
10 Pharmacokinetics and disposition of the oxytocin receptor antagonist L-368,899 in rats and dogs. Drug Metab Dispos. 1997 Oct;25(10):1113-8.
11 Oral oxytocin antagonists. J Med Chem. 2010 Sep 23;53(18):6525-38.
12 In vivo activity of the potent oxytocin antagonist on uterine activity in the rat. In Vivo. 2004 Nov-Dec;18(6):763-6.
13 Clinical pipeline report, company report or official report of darkpharma.
14 Design and synthesis of the first selective agonists for the rat vasopressin V(1b) receptor: based on modifications of deamino-[Cys1]arginine vasop... J Med Chem. 2007 Feb 22;50(4):835-47.
15 Synthesis and characterization of fluorescent antagonists and agonists for human oxytocin and vasopressin V(1)(a) receptors. J Med Chem. 2002 Jun 6;45(12):2579-88.
16 Characterization of the human oxytocin receptor stably expressed in 293 human embryonic kidney cells. Life Sci. 1995;57(24):2253-61.
17 Discovery and development of a new class of potent, selective, orally active oxytocin receptor antagonists. J Med Chem. 2005 Dec 1;48(24):7882-905.
18 Pharmacology of (2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methoxyimino) -1-[(2'-methyl[1,1'-biphenyl]-4-yl)carbonyl]-2-pyrrolidinecarboxamide, a ... J Pharmacol Exp Ther. 2003 Jul;306(1):253-61.
19 2,5-diketopiperazines as potent, selective, and orally bioavailable oxytocin antagonists. 2. Synthesis, chirality, and pharmacokinetics. J Med Chem. 2005 Nov 3;48(22):6956-69.
20 SSR126768A (4-chloro-3-[(3R)-(+)-5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl]-N-ethyl-N-(3-pyridylmethyl)-benzamide, ... J Pharmacol Exp Ther. 2004 Apr;309(1):414-24.
21 A nonpeptide oxytocin receptor antagonist radioligand highly selective for human receptors. Eur J Pharmacol. 2002 Aug 16;450(1):19-28.
22 Synthesis and biological activity of oxytocin analogues containing conformationally-restricted residues in position 7. Eur J Med Chem. 2007 Jun;42(6):799-806.
23 Toward efficient drug screening by homogeneous assays based on the development of new fluorescent vasopressin and oxytocin receptor ligands. J Med Chem. 2007 Oct 4;50(20):4976-85.
24 Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin. FEBS Lett. 1996 Nov 18;397(2-3):201-6.
25 [3H]-[Thr4,Gly7]OT: a highly selective ligand for central and peripheral OT receptors. Am J Physiol. 1988 Jan;254(1 Pt 1):E31-8.