Cart
sales@molnova.com
CLINODISIDE A
CAS No. 916347-31-4
CLINODISIDE A( —— )
Catalog No. M19260 CAS No. 916347-31-4
Clinodiside A in rats with one compartment open model into the body, rapid distribution, elimination rate.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 33 | In Stock |
|
| 5MG | 53 | In Stock |
|
| 10MG | 88 | In Stock |
|
| 25MG | 161 | In Stock |
|
| 50MG | 235 | In Stock |
|
| 100MG | 352 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCLINODISIDE A
-
NoteResearch use only, not for human use.
-
Brief DescriptionClinodiside A in rats with one compartment open model into the body, rapid distribution, elimination rate.
-
DescriptionClinodiside A in rats with one compartment open model into the body, rapid distribution, elimination rate.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetROCK
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number916347-31-4
-
Formula Weight959.13
-
Molecular FormulaC48H78O19
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (104.26 mM)
-
SMILESO1C(C(C(C(C1CO)O)O)O)OCC1OC(C(C(C1OC1OC(C(C(C1O)O)O)CO)O)O)OC1CCC2(C(C1)C(CC1(C3(CC(C4(CCC(CC4=C3C=CC21)(C)C)CO)O)C)C)(C)CO)C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Xue SR,et al. Triterpenoid saponins from Clinopodium polycephalum. Phytochemistry. 1992 Mar;31(3):1049-50.
molnova catalog
related products
-
Netarsudil mesylate
Netarsudil mesylate (AR-13324 mesylate) is a Rho-related protein kinase inhibitor used to study glaucoma and hypertension.
-
BDP5290
BDP5290 is a potent inhibitor of both ROCK and MRCK(IC50s of 5 nM 50 nM 10 nM and 100 nM for ROCK1 ROCK2 MRCKα and MRCKβ respectively.)
-
Y-33075 dihydrochlor...
Y-33075 dihydrochloride is a selective inhibitor of ROCK(IC50 of 3.6 nM).Y-33075 (Y-39983) is a potent inhibitor of ROCK(IC50 of 3.6 nM). Y-33075 also inhibits PKC and CaMKII more potently than Y-27632(IC50s of Y-27632 and Y-33075 for PKC are 9.0 μM and 0.42 μM, respectively), whereas the IC50s of Y-27632 and Y-33075 for CaMKII are 26 μM and 0.81 μM, respectively.
