GL Biochem (Shanghai) Ltd.
China
Product Name: (D-2-Nal5,Cys6·11,Tyr7,D-Trp8,Val10,2-Nal12)-Somatostatin-14 (5-12) amide
Price: $Inquiry/1g
Purity: 98.0%
Stocking Period: Inquiry
Contact: Jackie Yang

Taiwan Oyi peptide Co. Ltd
China
Product Name: (D-2-NAL5,CYS6·11,TYR7,D-TRP8,VAL10,2-NAL12)-SOMATOSTATIN-14 (5-12) AMIDE
Price: $Inquiry/1mg $Inquiry/100kg
Purity: 98.0%
Stocking Period: 1 Day
Contact: Vinnie

111857-96-6

111857-96-6 structure

Name: BIM 23042 TFA
Chemical Name: h-d-2-nal-cys-tyr-d-trp-lys-val-cys-2-nal-nh2
CAS Number: 111857-96-6
Molecular Formula: C₆₂H₇₃N₁₁O₉S₂
Molecular Weight: 1192.452
Catalog: Signaling Pathways GPCR/G Protein Bombesin Receptor
Create Date: 2018-12-11 11:04:20
Modify Date: 2024-01-13 08:39:32
BIM 23042, a certain somatostatin (SS) octapeptide analogue, is a selective neuropeptide neuromedin B receptor (NMB-R, BB1) antagonist. BIM 23042 has 100-fold lower affinity for gastrin-releasing peptide (GRP) receptor (BB2). BIM 23042 inhibits Neuromedin B (HY-P0241), ICI 216140 and DPDM-bombesin ethylamide-induced Ca2+ release[1][2][3].

Name	h-d-2-nal-cys-tyr-d-trp-lys-val-cys-2-nal-nh2
Synonyms	1,2-Dithia-5,8,11,14,17-pentaazacycloeicosane-4-carboxamide, 10-(4-aminobutyl)-N-[(1R)-2-amino-1-(2-naphthalenylmethyl)-2-oxoethyl]-19-[[(2R)-2-amino-3-(2-naphthalenyl)-1-oxopropyl]amino]-16-[(4-hydroxyphenyl)methyl]-13-(1H-indol-3-ylmethyl)-7-(1-methylethyl)-6,9,12,15,18-pentaoxo-, (4R,7S,10S,13R,16S,19R)- (4R,7S,10S,13R,16S,19R)-10-(4-Aminobutyl)-N-[(2R)-1-amino-3-(2-naphthyl)-1-oxo-2-propanyl]-19-{[(2R)-2-amino-3-(2-naphthyl)propanoyl]amino}-16-(4-hydroxybenzyl)-13-(1H-indol-3-ylmethyl)-7-isopropyl-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosane-4-carboxamide

Description	BIM 23042, a certain somatostatin (SS) octapeptide analogue, is a selective neuropeptide neuromedin B receptor (NMB-R, BB1) antagonist. BIM 23042 has 100-fold lower affinity for gastrin-releasing peptide (GRP) receptor (BB2). BIM 23042 inhibits Neuromedin B (HY-P0241), ICI 216140 and DPDM-bombesin ethylamide-induced Ca2+ release[1][2][3].
Related Catalog	Research Areas >> Metabolic Disease Signaling Pathways >> GPCR/G Protein >> Bombesin Receptor Research Areas >> Neurological Disease
In Vitro	BIM 23042 (5 μM) 在 huNMBR 细胞中竞争性抑制 Neuromedin B 诱导的 [3H] 花生四烯酸释放，Ki 为 49 nM[1]。
In Vivo	BIM 23042 (10μg; 静脉给药; 单次推注) 可减轻神经源性肿胀和热和机械致敏[2]。 Animal Model: Mice were 25-30 g male C57BL/6[2] Dosage: 10 μg Administration: IV; a single bolus Result: Attenuated neurogenic swelling and thermal and mechanical sensitization.
References	[1]. R R Ryan, et al. Pharmacological profiles of two bombesin analogues in cells transfected with human neuromedin B receptors. Eur J Pharmacol. 1996 Jun 13;306(1-3):307-14. [2]. Santosh K Mishra, et al. A nociceptive signaling role for neuromedin B. J Neurosci. 2012 Jun 20;32(25):8686-95. [3]. M Orbuch, et al. Discovery of a novel class of neuromedin B receptor antagonists, substituted somatostatin analogues. Mol Pharmacol. 1993 Oct;44(4):841-50.