PD 123319
CAS No. 130663-39-7
PD 123319( PD123319 | PD-123319 | (S)-(+)-PD 123319 )
Catalog No. M11225 CAS No. 130663-39-7
A potent, selective, non-peptide AT2 receptor with IC50 of 34 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 90 | In Stock |
|
| 2MG | 36 | In Stock |
|
| 5MG | 70 | In Stock |
|
| 10MG | 107 | In Stock |
|
| 25MG | 219 | In Stock |
|
| 50MG | 279 | In Stock |
|
| 100MG | 363 | In Stock |
|
| 200MG | 516 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NamePD 123319
-
NoteResearch use only, not for human use.
-
Brief DescriptionA potent, selective, non-peptide AT2 receptor with IC50 of 34 nM.
-
DescriptionA potent, selective, non-peptide AT2 receptor with IC50 of 34 nM.Heart Failure Discontinued.
-
In VitroPD 123319 is shown to discriminate between two subclasses of AII receptors in many different tissues.?125I-AII specifically label two classes of binding sites for AII in a membrane preparation of bovine adrenal glomerulosa cells. The first class (DuP-753 sensitive) represents approximately 85% of the total binding sites for AII and possesses a high affinity (IC50 of 92.9 nM) for DuP-753. PD-123319 does not have any effect on?125I-AII binding to this site. The second class of binding sites is more sensitive to PD-123319, with an IC50 of 6.9 nM, and has a much lower affinity for DuP-753 (IC50 around 10 microM).?
-
In Vivo——
-
SynonymsPD123319 | PD-123319 | (S)-(+)-PD 123319
-
PathwayGPCR/G Protein
-
TargetAngiotensin Receptor
-
RecptorAT2receptor
-
Research AreaCardiovascular Disease
-
Indication——
Chemical Information
-
CAS Number130663-39-7
-
Formula Weight508.6108
-
Molecular FormulaC31H32N4O3
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESCC1=C(C=CC(=C1)CN2C=NC3=C2C[C@H](N(C3)C(=O)C(C4=CC=CC=C4)C5=CC=CC=C5)C(=O)O)N(C)C
-
Chemical Name1H-Imidazo[4,5-c]pyridine-6-carboxylic acid, 1-[[4-(dimethylamino)-3-methylphenyl]methyl]-5-(2,2-diphenylacetyl)-4,5,6,7-tetrahydro-, (6S)-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
C-Type Natriuretic P...
CNP, a member of the natriuretic peptide family, was first identified in porcine brain and later found in other mammals as well as non-mammals. Processing of the CNP precursor gives rise to CNP-22 and its N-terminally elongated form, CNP-53. The CNPs share considerable sequence homology with ANP and BNP within the disulfide loop and exert similar pharmacological actions, although with different relative potencies.
-
Sparsentan
Sparsentan (RE-021) is a highly potent dual angiotensin II and endothelin A receptor antagonist with Kis of 0.8 and 9.3 nM, respectively.
-
TD-0212
TD-0212 (TD0212) is a potent, orally efficacious, dual AT1 antagonist/Neprilysin (NEP) inhibitor with pKi of 8.9 (AT1) and pIC50 of 9.2 (NEP).
Cart
sales@molnova.com