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BIO5192

Chemical Structure : BIO5192

CAS No.: 327613-57-0

BIO5192 (BIO-5192, BIO 5192)

Catalog No.: PC-61300Not For Human Use, Lab Use Only.

BIO5192 (BIO-5192) is a potent, highly selective inhibitor of integrin α4β1 (VLA-4) with Kd of <10 pM, IC50 of 1.8 nM.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

BIO5192 (BIO-5192) is a potent, highly selective inhibitor of integrin α4β1 (VLA-4) with Kd of <10 pM, IC50 of 1.8 nM.
BIO5192 displays selectively over a range of other integrins (IC50 are 138, 1053, > 500 and > 10,000 nM for α9β1, α2β1, α4β7 and αIIbβ3, respectively).
BIO5192 mobilizes hematopoietic stem and progenitor cells (HSPCs) alone or combined with plerixafor (AMD3100).

Physicochemical Properties

M.Wt 817.78
Formula C38H46Cl2N6O8S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(2S)-2-[[[(2S)-1-[(3,5-Dichlorophenyl)sulfonyl]-2-pyrrolidinyl]carbonyl]amino]-4-[[(2S)-4-methyl-2-[methyl[2-[4-[[[(2-methylphenyl)amino]carbonyl]amino]phenyl]acetyl]amino]-1-oxopentyl]amino]butanoic acid

References

1. Leone DR, et al. J Pharmacol Exp Ther. 2003 Jun;305(3):1150-62.

2. Theien BE, et al. Blood. 2003 Dec 15;102(13):4464-71.

3. Ramirez P, et al. Blood. 2009 Aug 13;114(7):1340-3.

4. Bao F, et al. Exp Neurol. 2008 Dec;214(2):160-7.

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