ChemicalBook--->CAS DataBase List--->477775-14-7

477775-14-7

477775-14-7 Structure

477775-14-7 Structure
IdentificationBack Directory
[Name]

M 24
[CAS]

477775-14-7
[Synonyms]

Buloxibutid
AT2 Agonist C21
AT2 Agonist C21 (M24)
T2 Agonist Compound 21
AT2 receptor agonist C21
Carbamic acid, N-[[3-[4-(1H-imidazol-1-ylmethyl)phenyl]-5-(2-methylpropyl)-2-thienyl]sulfonyl]-, butyl ester
[Molecular Formula]

C23H29N3O4S2
[MDL Number]

MFCD26936332
[MOL File]

477775-14-7.mol
[Molecular Weight]

475.62
Chemical PropertiesBack Directory
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 5 mg/mL (10.51 mM)
[form ]

A solid
[pka]

4.32±0.10(Predicted)
[color ]

White to yellow
[InChIKey]

XTEOJPUYZWEXFI-UHFFFAOYSA-N
[SMILES]

C(OCCCC)(=O)NS(C1SC(CC(C)C)=CC=1C1=CC=C(CN2C=NC=C2)C=C1)(=O)=O
Hazard InformationBack Directory
[Uses]

Buloxibutid (AT2 receptor agonist C21) is a agentlike selective angiotensin II AT2 receptor agonist with Ki values of 0.4 nM and >10 μM for the AT2 receptor and AT1 receptor, respectively[1].
[in vivo]

Buloxibutid, with a bioavailability of 20-30% after oral administration and a half-life estimated to 4 h in rat, induces outgrowth of neurite cells, stimulates p42/p44mapk, enhances in vivo duodenal alkaline secretion in Sprague-Dawley rats, and lowers the mean arterial blood pressure in anesthetized, spontaneously hypertensive rats[1].

[IC 50]

AT2 Receptor: 0.4 nM (Ki); AT1 Receptor: >10 μM (Ki)
[References]

[1] Wan Y, et al. Design, synthesis, and biological evaluation of the first selective nonpeptide AT2 receptor agonist. J Med Chem. 2004 Nov 18;47(24):5995-6008. DOI:10.1021/jm049715t
[2] Schwengel K, Namsolleck P, Lucht K, et al. Angiotensin AT2-receptor stimulation improves survival and neurological outcome after experimental stroke in mice. J Mol Med (Berl). 2016;94(8):957-966. DOI:10.1007/s00109-016-1406-3
[3] Fatima N, Patel S, Hussain T. Angiotensin AT2 Receptor is Anti-inflammatory and Reno-Protective in Lipopolysaccharide Mice Model: Role of IL-10. Front Pharmacol. 2021;12:600163. DOI:10.3389/fphar.2021.600163
Spectrum DetailBack Directory
[Spectrum Detail]

M 24(477775-14-7)1HNMR
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