Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN320205 Blarcamesine hydrochloride 195615-84-0
Anavex 2-73, an aminotetrahydrofuran derivative, is a mixed muscarinic and sigma-1/σ1 Receptor agonist with IC50 of 0.86 μM.
YN1730116 Exendin (5-39) 196109-27-0
Exendin (5-39) is a potent glucagon-like peptide 1 (GLP-1) receptor antagonist. Exendin (5-39) improves memory impairment in β-amyloid protein-treated rats.
YN483864 Prosaptide Tx14(A) 196391-82-9
Prosaptide Tx14(A), a prosaposin-derived peptide, is a potentGPR37L1 and GPR37agonist with EC50s of 5 and 7nM, respectively. Prosaptide Tx14(A) increases both ERK1 and ERK2 phosphorylation in Schwann cells.
YN321325 Ramelteon 196597-26-9
Ramelteon is a novel melatonin receptor agonist for human MT1 and MT2 receptors and chick forebrain melatonin receptors with Ki of 14 pM, 112 pM and 23.1 pM, respectively.
GW1929 is a potentPPAR-γagonist, with a pKi of 8.84 for humanPPAR-γ, and pEC50s of 8.56 and 8.27 for humanPPAR-γ and murinePPAR-γ, respectively.
NTR 368 is a peptide derived from p75 neurotrophin receptor (p75NTR) corresponding to residues 368-381 of the human receptor. NTR 368 has helix forming propensity in the presence of micellar lipid. NTR 368 is a potent inducer o...
LY367385 is a highly potent and selectivemGluR1aantagonist. LY367385 has an IC50 of 8.8μM for inhibits of quisqualate-induced phosphoinositide (PI) hydrolysis, compared with > 100μM for mGlu5a. LY367385 has neuroprotectiv...
YN480781 Ro 61-8048 199666-03-0
Ro 61-8048 is a high-affinity kynurenine 3-hydroxylase (KMO) inhibitor with IC50 and Ki of 37 nM and 4.8 nM, respectively.
YN321330 Paliperidone palmitate 199739-10-1
Paliperidone palmitate (9-Hydroxyrisperidone palmitate), an atypical long-acting antipsychotic agent, is an ester prodrug of Paliperidone. Paliperidone is adopamineantagonist and 5-HT2Aantagonist of the atypical antipsychotic class....
YN320982 RS-127445 hydrochloride 199864-86-3
RS-127445 hydrochloride is a selective, high affinity, orally bioavailable5-HT2Breceptorantagonist with a pKi of 9.5. RS-127445 hydrochloride shows 1000 fold selectivity for this receptor as compared to numerous other receptor and ...
YN320983 RS-127445 199864-87-4
RS-127445 is a selective 5-HT2B receptor antagonist with pKi of 9.5 and pIC50 of 10.4, exhibits >1000-fold selectivity against other 5-HT receptors.
YN270340 Omigapil maleate 200189-97-5
Omigapil maleate, an orally bioavailableGAPDH nitrosylationinhibitor, abrogates Aβ1-42-induced tau acetylation, memory impairment, and locomotor dysfunction in mice. Omigapil maleate has the potential for the research of Alzheim...
YN320236 SB 243213 200940-22-3
SB 243213 is an orally active, selective and high-affinity5-HT2Creceptorantagonist with a pKi of 9.37 and apKbof 9.8 for human 5-HT2Creceptor. SB 243213 shows greater than a 100-fold selectivity over a wide range of neurotra...
YN320234 SB 243213 hydrochloride 200940-23-4
SB 243213 hydrochloride is an orally active, selective and high-affinity5-HT2Creceptorantagonist with a pKi of 9.37 and apKbof 9.8 for human 5-HT2Creceptor. SB 243213 hydrochloride shows greater than a 100-fold selectivity o...
YN321905 Ac-RYYRWK-NH2 200959-47-3
Ac-RYYRWK-NH2 is a potent and selective partial agonist for thenociceptin receptor (NOP), [3H]Ac-RYYRWK-NH2 binds to rat cortical membranes ORL1 with aKdof 0.071nM, but has no affinity for µ-, κ- or δ-opioid ...
YN321908 Ac-RYYRIK-NH2 200959-48-4
Ac-RYYRIK-NH2 is a potent and partial agonist onORL1transfected in CHO cells (Kd=1.5nM) and behaves as a endogenous lig and of ORL1. Ac-RYYRIK-NH2 is a specific antagonist for the activation of G protein ...
YN320967 SB-269970 201038-74-6
SB269970 is a5-HT7 receptorantagonist withpKiof 8.3, exhibits >50-fold selectivity against other receptors.
YN380279 Autocamtide-2-related inhibit... 201422-04-0
Autocamtide-2-related inhibitory peptide, myristoylated is the myristoylated Autocamtide-2-related inhibitory peptide. Autocamtide-2-related inhibitory peptide is a highly specific and potent inhibitor ofCaMKIIwith an IC50 of 40...
LY341495 is ametabotropic glutamate receptor (mGluR)antagonist with IC50s of 21nM, 14nM, 7.8μM, 8.2μM, 170nM, 990nM, 22μM for mGlu2, mGlu3, mGlu1a, mGlu5a, mGlu8, mGlu7, and mGlu4 receptors, respectively..
GET73 is a γ-hydroxybutyric acid (GHB) analog, a naturally occurring neurotransmitter. GET73 has anti-alcohol and anxiolytic properties. GET73 significantly affects glutamate transmission in the hippocampus .
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