Home   >  
Ion Channel/Membrane Transporter
  • Neuro Signaling Pathway
∨
  >  
nAChR

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

nAChR

Chemical Structure Cat. No. Product Name CAS No.
Myosmine Chemical Structure
 BCP47943 Myosmine 532-12-7
Myosmine, a specific tobacco alkaloid in nuts and nut products, has low affinity for a4b2 nicotinic acetylcholinergic receptors (nAChR) with a Ki of 3300 nM.
NS1738 Chemical Structure
 BCP46794 NS1738 501684-93-1
NS1738 is a α7 positive allosteric modulator.
Anagyrin Chemical Structure
 BCP44368 Anagyrin 486-89-5
Anagyrine is an alkaloid that has been found in L. albus and has nematocidal and anticancer activities.
ABT-418 hydrochloride Chemical Structure
 BCP38433 ABT-418 hydrochloride 147388-83-8
ABT-418 hydrochloride is a neuronal nicotinic acetylcholine receptor agonist.
4BP-TQS Chemical Structure
 BCP37825 4BP-TQS 360791-49-7
4BP-TQS is an allosteric agonist of α7 subunit-containing neuronal nicotinic acetylcholine receptors (nAChRs).
PSEM 89S TFA Chemical Structure
 BCP35173 PSEM 89S TFA 1336913-03-1
PSEM 89S TFA is a selective and brain penetrant agonists for the resulting ion channels. PSEM 89S TFA is orthogonally selective for Q79G and L141F, respectively.
CCMI Chemical Structure
 BCP35052 CCMI 917837-54-8
CCMI is a potent and selective α7 nAChR-positive allosteric modulator, does not bind to or activate α7 nAChRs via the orthosteric site, and causes significant positive modulation of agonist-induced currents at α7 nAChRs. CCMI has potential in CNS diseases with cognitive dysfunction.
nAChR agonist 1 Chemical Structure
 BCP33344 nAChR agonist 1 1394371-75-5
nAChR agonist 1 is a potent, brain-permeable, and orally efficacious positive allosteric modulator of α7 nicotinic acetylcholine receptor (α7 nAChR).
Facinicline hydrochloride Chemical Structure
 BCP33359 Facinicline hydrochloride 677305-02-1
PNU-282987 S enantiomer free base Chemical Structure
 BCP25435 PNU-282987 S enantiomer free base 737727-12-7
PNU-282987 is a highly selective α7 nAChR agonist (Ki = 26 nM) displaying negligible blockade of α1β1γδ and α3β4 nAChRs (IC50 ≥ 60 μM).
12下一页共 20 条记录 1 / 2 页 
0086-13720134139