147819-32-7

JB-1 Chemical Structure
147819-32-7

Chemical Structure

JB-1

  • CAS No.: 147819-32-7
  • Formula:C55H88N14O15S2
  • Molecular Weight:1249.50

IUPAC Name: (6S,9S,12S,15R,20R,23S,26S,29S,31aS,37S,40S,42aS)-15-amino-26,37-bis(4-aminobutyl)-12-(4-hydroxybenzyl)-23-(hydroxymethyl)-40-isobutyl-6,9,29-trimethyl-5,8,11,14,22,25,28,31,36,39,42-undecaoxooctatriacontahydro-1H,19H-dipyrrolo[2,1-p:2',1'-y][1,2]dithia[5,8,11,14,17,20,23,26,29,32,35]undecaazacyclooctatriacontine-20-carboxylic acid

InChIKey: MPUVBZQBFGGAAS-XHGDPFBQSA-N

SMILES: O=C1N2[C@@](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CSSC[C@@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N3[C@](CCC3)([H])C(N[C@H](C(N[C@H]1CCCCN)=O)CC(C)C)=O)=O)C)=O)C)=O)CC4=CC=C(C=C4)O)=O)N)C(O)=O)=O)CO)=O)CCCCN)=O)C)=O)([H])CCC2

Biological Activity: JB-1, an IGF-I analog, is a selective IGF-I receptor inhibitor that does not interact with IGF-II. JB-1 competes with IGF-I for binding to IGF-1R and blocks receptor autophosphorylation. JB-1 increases the level of sVEGFR-1. JB-1 normalizes retinal abnormalities, including reducing retinal neovascularization. JB-1 is applicable to studies related to oxygen-induced retinopathy[1].

Cat. No. Product Name Purity Description Pricing
HY-P3226
JB-1 99.63% JB-1, an IGF-I analog, is a selective IGF-I receptor inhibitor that does not interact with IGF-II. JB-1 competes with IGF-I for binding to IGF-1R and blocks receptor autophosphorylation. JB-1 increases the level of sVEGFR-1. JB-1 normalizes retinal abnormalities, including reducing retinal neovascularization. JB-1 is applicable to studies related to oxygen-induced retinopathy.
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