AS 602801
CAS No. 848344-36-5
AS 602801( AS602801 | PGL-5001 | PGL 5001 | Bentamapimod )
Catalog No. M17611 CAS No. 848344-36-5
AS 602801(Bentamapimod) is a novel, orally active inhibitor of JNK.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 34 | In Stock |
|
| 5MG | 55 | In Stock |
|
| 10MG | 91 | In Stock |
|
| 25MG | 149 | In Stock |
|
| 50MG | 186 | In Stock |
|
| 100MG | 332 | In Stock |
|
| 500MG | 1089 | In Stock |
|
| 1G | 1971 | In Stock |
|
Biological Information
-
Product NameAS 602801
-
NoteResearch use only, not for human use.
-
Brief DescriptionAS 602801(Bentamapimod) is a novel, orally active inhibitor of JNK.
-
DescriptionBentamapimod, also known as AS602801 and PGL5001, is a JNK Inhibitor. AS602801 induces regression of endometriotic lesions in animal models. AS602801 interrupts immune pathways. Bentamapimod induced regression of endometriotic lesions in endometriosis rodent animal models without suppressing ER action. Endometriosis is an estrogen (ER)-dependent gynecological disease caused by the growth of endometrial tissue at extrauterine sites.
-
In Vitro——
-
In Vivo——
-
SynonymsAS602801 | PGL-5001 | PGL 5001 | Bentamapimod
-
PathwayOthers
-
TargetOther Targets
-
RecptorJNK1| JNK2| JNK3
-
Research AreaInflammation/Immunology
-
Indication——
Chemical Information
-
CAS Number848344-36-5
-
Formula Weight457.55
-
Molecular FormulaC25H23N5O2S
-
Purity>98% (HPLC)
-
SolubilityDMSO : 14.29 mg/mL. 31.23 mM;
-
SMILESN#CC(c1nc2ccccc2s1)c1nc(OCc2ccc(CN3CCOCC3)cc2)ncc1
-
Chemical Name2-(1,3-benzothiazol-2-yl)-2-[2-({4-[(morpholin-4-yl)methyl]phenyl}methoxy)pyrimidin-4-yl]acetonitrile
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Ferrandi C, et al. Mult Scler. 2011 Jan;17(1):43-56.
molnova catalog
related products
-
Gluconasturtiin
The herbs of Nasturtium officinale.
-
Ganoderenic acid A
Ganoderenic acid A has a potent hepatoprotective, and cytotoxic effects, it shows inhibitory activity on human aldose reductase in vitro.From the acidic fraction, potent human aldose reductase inhibitors, ganoderic acid C2 (1) and Ganoderenic acid A (2), were isolated together with three related compounds.
-
Allisartan Isoproxil
Allisartan Isoproxil, an angiotensin II receptor antagonist, is used to treat mild to moderate essential hypertension.
Cart
sales@molnova.com