YPX-C-05
CAS No. 2894823-79-9
YPX-C-05( —— )
Catalog No. M37338 CAS No. 2894823-79-9
YPX-C-05 is an isohydroxamic acid derivative and HDAC inhibitor with vasodilatory and antihypertensive activity.YPX-C-05 is used in the study of hypertension and vascular related disorders.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 296 | Get Quote |
|
| 5MG | 459 | Get Quote |
|
| 10MG | 657 | Get Quote |
|
| 25MG | 994 | Get Quote |
|
| 50MG | 1371 | Get Quote |
|
| 100MG | 1773 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameYPX-C-05
-
NoteResearch use only, not for human use.
-
Brief DescriptionYPX-C-05 is an isohydroxamic acid derivative and HDAC inhibitor with vasodilatory and antihypertensive activity.YPX-C-05 is used in the study of hypertension and vascular related disorders.
-
DescriptionYPX-C-05 is a hydroxamic acid-based HDAC inhibitor. YPX-C-05 exerts significant vasodilatory effects. YPX-C-05 exhibits inhibitory effects on HDACs and increases histone H4 acetylation in endothelial cells. YPX-C-05 can be used for hypertension research.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetHDAC
-
RecptorHDAC
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2894823-79-9
-
Formula Weight377.39
-
Molecular FormulaC21H19N3O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(NC=1C=CC(=CC1)C2=CC=CC(OC)=C2)NC3=CC=C(C=C3)C(=O)NO
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Pang PP, et al. The hydroxamic acid derivative YPX-C-05 alleviates hypertension and vascular dysfunction through the PI3K/Akt/eNOS pathway. Vascul Pharmacol. 2023 Dec 3;154:107251. ?
molnova catalog
related products
-
Givinostat
Givinostat hydrochloride monohydrate is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively.
-
TH34
TH34 is an HDAC6/8/10 inhibitor (IC50s: 4.6/1.9/7.7 μM). It shows high selectivity over HDAC1/2/3.
-
(2R/S)-6-PNG
(2R/S)-6-PNG (6-Prenylnaringenin) is a novel natural histone deacetylase inhibitor with anticancer and antitumor activity, and it blocks T-type calcium channels to reduce neuropathic and visceral pain in mice.
Cart
sales@molnova.com