Chroman 1
CAS No. 1273579-40-0
Chroman 1( —— )
Catalog No. M26648 CAS No. 1273579-40-0
Chroman 1 is a potent inhibitor of ROCK1 (IC50?= 52 pM) and ROCK2 (IC50?= 1 pM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 155 | In Stock |
|
| 10MG | 250 | In Stock |
|
| 25MG | 460 | In Stock |
|
| 50MG | 668 | In Stock |
|
| 100MG | 888 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameChroman 1
-
NoteResearch use only, not for human use.
-
Brief DescriptionChroman 1 is a potent inhibitor of ROCK1 (IC50?= 52 pM) and ROCK2 (IC50?= 1 pM).
-
DescriptionChroman 1 is a potent inhibitor of ROCK1 (IC50?= 52 pM) and ROCK2 (IC50?= 1 pM).(In Vitro):Chroman 1 showed inhibitory activities against MRCK (IC50: 150 nM). However, it has no effect on PKA (IC50, > 20000 nM) or AKT1 (IC50, > 20000 nM).
-
In VitroApoptosis Analysis Cell Line:hESCs (human pluripotent stem cells) (WA09)Concentration:50 nMIncubation Time:0-12 h or 24 h Result:Reduced the number of apoptotic cells, reduced caspase-3/7 activation.Western Blot Analysis Cell Line:hESCs (human pluripotent stem cells) (WA09)Concentration:50 nM Incubation Time:24 h Result:Partially inhibited caspase-3 activation.
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetROCK
-
Recptorinflammation
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1273579-40-0
-
Formula Weight436.512
-
Molecular FormulaC24H28N4O4
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : ≥ 50 mg/mL (114.55 mM)
-
SMILESCOc1ccc2OC[C@H](Cc2c1)C(=O)Nc1ccc(cc1OCCN(C)C)-c1cn[nH]c1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Stratmann J. Synthesis, structure elucidation and biological activity of thio- analogs of drugs with the examples of chlorthenoxazine and amobarbital. Pharmazie. 1990 Sep;45(9):668-70. German.
molnova catalog
related products
-
Netarsudil dihydroch...
Netarsudil (AR-13324) is a potent, selective ROCK inhibitor with Ki of 4.2 nM for ROCK2.
-
TG100713
TG100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.
-
Rhodblock 6
Rhodblock 6 is a Rho kinase (ROCK) inhibitor that specifically inhibits Rho kinase activity and the localization of phosphorylated MRLC (Myosin Regulatory Light Chain).
Cart
sales@molnova.com