Cart
sales@molnova.com
(R)-Nepicastat HCl
CAS No. 195881-94-8
(R)-Nepicastat HCl( —— )
Catalog No. M17411 CAS No. 195881-94-8
(R)-Nepicastat HCl, the R-enantiomer of Nepicastat HCl, is a potent and selective inhibitor with IC50 of 25.1 nM and 18.3 nM for bovine and human dopamine-β-hydroxylase, with negligible affinity for twelve other enzymes and thirteen neurotransmitter receptors.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 122 | Get Quote |
|
| 10MG | 206 | Get Quote |
|
| 25MG | 389 | Get Quote |
|
| 50MG | 527 | Get Quote |
|
| 100MG | 770 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product Name(R)-Nepicastat HCl
-
NoteResearch use only, not for human use.
-
Brief Description(R)-Nepicastat HCl, the R-enantiomer of Nepicastat HCl, is a potent and selective inhibitor with IC50 of 25.1 nM and 18.3 nM for bovine and human dopamine-β-hydroxylase, with negligible affinity for twelve other enzymes and thirteen neurotransmitter receptors.
-
Description(R)-Nepicastat HCl, the R-enantiomer of Nepicastat HCl, is a potent and selective inhibitor with IC50 of 25.1 nM and 18.3 nM for bovine and human dopamine-β-hydroxylase, with negligible affinity for twelve other enzymes and thirteen neurotransmitter receptors.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorDopamine β-hydroxylase| Dopamine β-hydroxylase
-
Research AreaCardiovascular Disease
-
Indication——
Chemical Information
-
CAS Number195881-94-8
-
Formula Weight331.81
-
Molecular FormulaC14H15F2N3S·HCl
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCl.NCC1=CNC(=S)N1[C@@H]1CCC2=C(F)C=C(F)C=C2C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Stanley WC, et al. Br J Pharmacol. 1997, 121(8), 1803-1809.
molnova catalog
related products
-
mPEG-DSPE sodium
mPEG-DSPE sodium (DSPE-mPEG2000 sodium) is a PROTAC linker belonging to PEG and is involved in the synthesis of PROTAC molecules.
-
Adoprazine
Adoprazine is a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.
-
Euphorbia factor L8
Euphorbia factor L8 is a natural product.
