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Y-27632+dihydrochloride
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Y-27632+dihydrochloride
Supplier:
AMBEED, INC
Description:
Y-27632 dihydrochloride 99%
Catalog Number:
(80512-706)
Supplier:
MilliporeSigma
Description:
A 5 mM (500 µg/296 µl) solution of Y-27632 (Cat. No. 688000) in H₂O.
Supplier:
Enzo Life Sciences
Description:
ROCK inhibitor
Supplier:
Adipogen
Description:
Potent, cell permeable, selective and ATP-competitive Rho-associated protein kinases inhibitor, including p160ROCK, ROCK-II and PRK2 inhibitor. Tumor cell invasion and metastasis suppressor. Smooth muscle relaxant. Decreases liver fibrosis by hepatic stellate cell growth inhibition. Antinociceptive. Blocks generation of inflammatory cytokines. Stem cell research modulator. Prevents apoptosis and enhances the survival and cloning efficiency of dissociated human embryonic stem (hES) cells without affecting their pluripotency. Increases survival rate of hES cells undergoing cryopreservation.
Supplier:
BIOGEMS INTERNATIONAL INC.
Description:
Y-27632 is a selective inhibitor of Rho-associated coiled-coil forming protein serine/threonine kinase (ROCK) family of protein kinases that selectively competes with ATP for binding to the catalytic site. It is reported to diminish dissociation-induced apoptosis, increase cloning efficiency, and facilitate subcloning after gene transfer in human embryonic stem cells (hES).
Supplier:
MilliporeSigma
Description:
A highly potent, cell-permeable, reversible, and selective inhibitor of Rho-associated protein kinases.
Catalog Number:
(77982-933)
Supplier:
LGC STANDARDS
Description:
Y-27632 Dihydrochloride, TRC, LGC Standards
Catalog Number:
(77694-253)
Supplier:
LGC STANDARDS
Description:
Y-27632 Dihydrochloride, TRC, LGC Standards
Catalog Number:
(103521-494)
Supplier:
IXCELLS BIOTECHNOLOGIES USA MS
Description:
Y-27632 ; 2mg (10 mm in 624.4 µL DMSO); Y-27632 is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nm in a cell-free assay, exhibits >200-fold selectivity over other kinases, including PKC, cAMP-dependent protein kinase, MLCK and PAK.
Supplier:
Enzo Life Sciences
Description:
A cell permeable, highly specific, potent and ATP-competitive inhibitor of Rho kinase (ROCK) (Ki=1.6nM). Exhibits a much weaker affinity for other serine/threonine kinases (Ki=630nM for PKA, 9.27mM for PKC and 10.1mM for MLCK). More potent and selective than Y-27632. Inhibits the phosphorylation of MARCKS in cells stimulated by lysophosphatidic acid. Inhibits EP3-stimulated NO formation. Prevents fragmentation of apoptotic cells. Relieves neuropathic pain.
Catalog Number:
(77599-620)
Supplier:
AMBEED, INC
Description:
Y-27632 ≥98%
Catalog Number:
(TCB2699-25G)
Supplier:
TCI America
Description:
CAS Number: 67006-34-2
Molecular Formula: C7H16O7S2 Molecular Weight: 276.32 Purity/Analysis Method: >93.0% (GC) Form: Crystal
Catalog Number:
(89147-880)
Supplier:
Enzo Life Sciences
Description:
A cell permeable, selective, and ATP-competitive inhibitor of Rho kinase (ROCK) activity (IC50=25µM). Does not inhibit the activation of Rho nor does it affect the in vitro activities of MLCK, PKCα, and SAPK2a/p38α. Shown to be less potent than Y-27632.
Catalog Number:
(77627-158)
Supplier:
AMBEED, INC
Description:
Benzylhydrazine dihydrochloride ≥96%
Supplier:
TCI America
Description:
(R)-(+)-3-Aminoquinuclidine Dihydrochloride, Purity: >98.0%(N)(T), Cas: 123536-14-1, Molecular Formula: C7H14N2.2HCl, Molecular Weight: 199.12, Synonyms: (R)-(+)-3-Amino-1-azabicyclo[2.2.2]octane Dihydrochloride, Application: Crystal powder, Size: 5G
Supplier:
Thermo Scientific Chemicals
Description:
L-Lysinamide dihydrochloride, 95%
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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