M 24
- Product Name
- M 24
- CAS No.
- 477775-14-7
- Chemical Name
- M 24
- Synonyms
- Buloxibutid;AT2 Agonist C21;AT2R Agonist C21;AT2 Agonist C21 (M24);T2 Agonist Compound 21;AT2 receptor agonist C21;Buloxibutid, 10 mM in DMSO;AT2 receptor agonist C21,AT-2 receptor agonist C21;Butyl (3-(4-((1H-imidazol-1-yl)methyl)phenyl)-5-isobutylthiophen-2-yl)sulfonylcarbamate;Carbamic acid, N-[[3-[4-(1H-imidazol-1-ylmethyl)phenyl]-5-(2-methylpropyl)-2-thienyl]sulfonyl]-, butyl ester
- CBNumber
- CB83146327
- Molecular Formula
- C23H29N3O4S2
- Formula Weight
- 475.62
- MOL File
- 477775-14-7.mol
M 24 Property
- 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
N-Bromosuccinimide Price
- Product number
- CS-0018094
- Product name
- AT2receptoragonistC21
- Purity
- 99.24%
- Packaging
- 5mg
- Price
- $120
- Updated
- 2021/12/16
- Product number
- CS-0018094
- Product name
- AT2receptoragonistC21
- Purity
- 99.24%
- Packaging
- 10mg
- Price
- $190
- Updated
- 2021/12/16
- Product number
- CS-0018094
- Product name
- AT2receptoragonistC21
- Purity
- 99.24%
- Packaging
- 25mg
- Price
- $350
- Updated
- 2021/12/16
- Product number
- CS-0018094
- Product name
- AT2receptoragonistC21
- Purity
- 99.24%
- Packaging
- 50mg
- Price
- $550
- Updated
- 2021/12/16
- Product number
- CS-0018094
- Product name
- AT2receptoragonistC21
- Purity
- 99.24%
- Packaging
- 100mg
- Price
- $950
- Updated
- 2021/12/16
M 24 Chemical Properties,Usage,Production
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
M 24 Preparation Products And Raw materials
Raw materials
Preparation Products
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