Cart
sales@molnova.com
(R)-Ambrisentan-d3
CAS No. 1007358-76-0
(R)-Ambrisentan-d3( —— )
Catalog No. M23102 CAS No. 1007358-76-0
(R)-Ambrisentan-d3 is the deuterated version of (R)-Ambrisentan (A575873), which is the R-isomer impurity of Ambrisentan (A575860) that is a nonpeptide endothelin ETA receptor antagonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 468 | In Stock |
|
| 25MG | 1020 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name(R)-Ambrisentan-d3
-
NoteResearch use only, not for human use.
-
Brief Description(R)-Ambrisentan-d3 is the deuterated version of (R)-Ambrisentan (A575873), which is the R-isomer impurity of Ambrisentan (A575860) that is a nonpeptide endothelin ETA receptor antagonist.
-
Description(R)-Ambrisentan-d3 is the deuterated version of (R)-Ambrisentan (A575873), which is the R-isomer impurity of Ambrisentan (A575860) that is a nonpeptide endothelin ETA receptor antagonist, used as antihypertensive drug.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1007358-76-0
-
Formula Weight378.42
-
Molecular FormulaC22H22N2O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES——
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Riechers, H., et al.: J. Med. Chem., 39, 2123 (1996); Billman, G.E., et al.: Curr. Opin. Invest. Drugs, 3, 1483 (2002); Vatter, H., et al.: Clin. Neuropharmacol., 26, 73 (2003)
molnova catalog
related products
-
Neratinib Maleate
Irreversible ErbB receptor tyrosine kinase inhibitor.
-
Sodium Hyaluronate
Hyaluronic acid (HA) is an anionic nonsulfated glycosaminoglycan distributed widely throughout connective epithelial and neural tissues. It is unique among glycosaminoglycans in that it is nonsulfated forms in the plasma membrane instead of the Golgi and can be very large with its molecular weight often reaching the millions.
-
Org41841
Org41841 is an agonist of luteinising hormone/chorionic gonadotropin receptor and thyroid stimulating hormone receptor (EC50s: 0.2 and 7.7 μM, respectively) and can be used to study hyperthyroidism.
