LX-7101 hydrochloride
CAS No. 1374644-80-0
LX-7101 hydrochloride( —— )
Catalog No. M34647 CAS No. 1374644-80-0
LX-7101 hydrochloride is a potent LIMK and ROCK2 inhibitor with antihypertensive activity, inhibits LIMK1/2, ROCK, PKA, and can be used to study glaucoma.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 459 | In Stock |
|
| 10MG | 657 | In Stock |
|
| 25MG | 1026 | In Stock |
|
| 50MG | 1386 | In Stock |
|
| 100MG | 1832 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameLX-7101 hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionLX-7101 hydrochloride is a potent LIMK and ROCK2 inhibitor with antihypertensive activity, inhibits LIMK1/2, ROCK, PKA, and can be used to study glaucoma.
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DescriptionLX-7101 hydrochloride is a potent LIMK and ROCK2 inhibitor with antihypertensive activity, inhibits LIMK1/2, ROCK, PKA, and can be used to study glaucoma.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayApoptosis
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TargetPKA
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RecptorPKA | ROCK | LIM Kinase
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Research Area——
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Indication——
Chemical Information
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CAS Number1374644-80-0
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Formula Weight487.99
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Molecular FormulaC23H29N7O3 xHCl
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Purity>98% (HPLC)
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Solubility——
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SMILESCl.O=C(OC1=CC=CC(=C1)NC(=O)C2(CN)CCN(C=3N=CN=C4NC=C(C43)C)CC2)N(C)C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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GSK-J4 Hydrochloride
GSK-J4 is a cell permeable, potent and selective histone demethylase(JMJD3 )inhibitor. is an ethyl ester derivative of the GSK-J1 with an IC50 value greater than 50 μM in vitro.
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HA-1004 dihydrochlor...
HA-1004 dihydrochloride?is an inhibitor of PKA, PKC, cGKI, MYLK, and calcium channel proteinHA-1004, was shown to be a potent inhibitor of two cyclic nucleotide-dependent protein kinases, cyclic GMP-dependent protein kinase and cyclic AMP-dependent protein kinase and the Ki values were 1.4 and 2.3 microM, respectively.?
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KT-5720
KT-5720 is a highly specific PKA (cAMP-dependent protein kinase) inhibitor with Ki of 60 nM displays little to no activity for MLCK, cGPK, and PKC (Ki>2 uM).
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