Cart
sales@molnova.com
PF-05221304
CAS No. 1370448-25-1
PF-05221304( NSC 170984, R 6238, STAT5 Inhibitor III )
Catalog No. M23101 CAS No. 1370448-25-1
PF-05221304 is an orally bioavailable, liver-targeted inhibitor of acetyl-CoA carboxylase (ACC), an enzyme that catalyzes the first committed step in de novo lipogenesis (DNL).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 255 | In Stock |
|
| 5MG | 167 | In Stock |
|
| 10MG | 252 | In Stock |
|
| 25MG | 437 | In Stock |
|
| 50MG | 556 | In Stock |
|
| 100MG | 809 | In Stock |
|
| 200MG | 1088 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NamePF-05221304
-
NoteResearch use only, not for human use.
-
Brief DescriptionPF-05221304 is an orally bioavailable, liver-targeted inhibitor of acetyl-CoA carboxylase (ACC), an enzyme that catalyzes the first committed step in de novo lipogenesis (DNL).
-
DescriptionPF-05221304 is an orally bioavailable, liver-targeted inhibitor of acetyl-CoA carboxylase (ACC), an enzyme that catalyzes the first committed step in de novo lipogenesis (DNL).
-
In Vitro——
-
In Vivo——
-
SynonymsNSC 170984, R 6238, STAT5 Inhibitor III
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1370448-25-1
-
Formula Weight502.57
-
Molecular FormulaC28H30N4O5
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCC(C)N1C2=C(CC3(CCN(C(C4=CC(C5=CC=C(C(O)=O)C=C5)=NC(OC)=C4)=O)CC3)CC2=O)C=N1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
(Diacetyl)-α-MSH
(Diacetyl)-α-MSH
-
ML221
ML221 is a potent?apelin /APJ?functional antagonist, inhibiting apelin-13-mediated activation of APJ, with?IC50s of 0.70 μM in the cAMP assay, and 1.75 μM in the β-arrestin assay, and?EC80?of 10 nM in both assays.
-
Cevipabulin
Cevipabulin (TTI-237) is a microtubule-active antitumor compound and inhibits the binding of [3H] vinblastine to tubulin (IC50: 18-40 nM in the human tumor cell line).
