ChemicalBook--->CAS DataBase List--->60786-59-6

60786-59-6

60786-59-6 Structure

60786-59-6 Structure
IdentificationBack Directory
[Name]

CYS-TYR-ILE-THR-ASN-CYS-GLY-LEU-GLY-NH2
[CAS]

60786-59-6
[Synonyms]

TGOT
(THR4
GLY7)-OXYTOCIN
[THR4, GLY7] OT
[THR4, GLY7]-OXYTOCIN
thr(4)-gly(7)-oxytoci
3,3-DiallylthiacarbocyanineBromide
CYS-TYR-ILE-THR-ASN-CYS-GLY-LEU-GLY-NH2
H-CYS-TYR-ILE-THR-ASN-CYS-GLY-LEU-GLY-NH2
H-CYS-TYR-ILE-THR-ASN-CYS-GLY-LEU-GLY-NH2, (DISULFIDE BOND)
Cys-Tyr-Ile-Thr-Asn-Cys-Gly-Leu-Gly-NH2 (Disulfide bridge Cys1-Cys6)
(Thr4,Gly7)-Oxytocin H-Cys-Tyr-Ile-Thr-Asn-Cys-Gly-Leu-Gly-NH2 (Disulfide bond)
Glycinamide, L-cysteinyl-L-tyrosyl-L-isoleucyl-L-threonyl-L-asparaginyl-L-cysteinylglycyl-L-leucyl-, cyclic (1→6)-disulfide
[Molecular Formula]

C39H61N11O12S2
[MDL Number]

MFCD00076735
[MOL File]

60786-59-6.mol
[Molecular Weight]

940.1
Chemical PropertiesBack Directory
[Boiling point ]

1489.4±65.0 °C(Predicted)
[density ]

1.265±0.06 g/cm3(Predicted)
[storage temp. ]

−20°C
[form ]

Solid
[pka]

9.90±0.15(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Hazard statements ]

H332
[Precautionary statements ]

P261-P271-P304+P340-P312a
[Hazard Codes ]

Xn
[Risk Statements ]

20
[Safety Statements ]

36/37/39-45
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

(Thr4,Gly7)-Oxytocin, an Oxytocin analogue, is a specific OT receptor agonist. (Thr4,Gly7)-Oxytocin also excites subicular neurons via activation of TRPV1 channels, and depression of K+ channels. [1][2].
[in vivo]

(Thr4,Gly7)-Oxytocin (1 μM, direct intra-PVT infusion for 1 min) evokes depolarization on TGOT-responsive neurons in mice[1].
(Thr4,Gly7)-Oxytocin (100 ng, intracerebroventrical injection) increases nitric oxide production in the paraventricular nucleus of the hypothalamus of male rats[3].

Animal Model:Swiss Webster mice [1]
Dosage:1 μM
Administration:Intratracheal administration for 24 h
Result:Excited 34.3% of aPVT neurons, 57.6% of mPVT neurons, and 60.0% of pPVT neurons.
Increased the firing rate of TGOT-responsive PVT neurons in all subregions.
[References]

[1] Lily R Barrett, et al. Oxytocin activation of paraventricular thalamic neurons promotes feeding motivation to attenuate stress-induced hypophagia. Neuropsychopharmacology. 2021 Apr;46(5):1045-1056. DOI:10.1038/s41386-021-00961-3
[2] Binqi Hu, et al. Activation of Oxytocin Receptors Excites Subicular Neurons by Multiple Signaling and Ionic Mechanisms. Cereb Cortex. 2021 Mar 31;31(5):2402-2415. DOI:10.1093/cercor/bhaa363
[3] M R Melis, et al. Oxytocin increases nitric oxide production in the paraventricular nucleus of the hypothalamus of male rats: correlation with penile erection and yawning. Regul Pept. 1997 Mar 26;69(2):105-11. DOI:10.1016/s0167-0115(97)00002-5
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