Chemical structure
Cat.No.
Product Name
CAS no.
Target
PLX5622 is a highly selective CSF-1R inhibitor (IC50 < 10 nmol/L), showing > 20-fold selectivity over KIT and FLT3.
YN320137 CHPG sodium salt 1303993-73-8
CHPG sodium salt is a selectivemGluR5agonist, and attenuates SO2-induced oxidative stress and inflammation throughTSG-6/NF-κBpathway in BV2 microglial cells. CHPG sodium salt protects against traumatic brain injury ...
NGP 555 is a small-molecule modulator of γ-secretase and has been successful in achieving good oral absorption, brain penetration, CNS activity, and specificity for a lipid-based membrane target preclinically.
YN320488 LY-2940094 1307245-86-8
LY-2940094 is a potent, selective and orally availablenociceptin receptor(NOP receptor) antagonist with high affinity (Ki=0.105nM) and antagonist potency (Kb=0.166nM). LY-2940094 reduces ethanol self-administration in animal ...
Ogerin is a selectiveGPR68positive allosteric modulator, with apEC50of 6.83. Ogerin shows inverse agonist and antagonist activity (Ki, 220nM) at A2Areceptoor and weak antagonist activity (Ki, 736nM) at 5-HT2Breceptor. O...
YN320765 SEP-363856 hydrochloride 1310422-41-3
SEP-363856 hydrochloride(SEP-856 hydrochloride), an orally active and CNS active psychotropic agent with a unique, non-D2/5-HT2A mechanism of action, exerts its antipsychotic-like effects. SEP-363856 hydrochloride(SEP...
PH-002 is an inhibitor ofapolipoprotein (apo) E4intramolecular domain interaction in neuronal cells that could rescue impairments of mitochondrial motility and neurite outgrowth.
YN321197 LY2812223 1311385-20-2
LY2812223 is a highly potent, functionally selectivemGlu2receptoragonist with mGlu2binding affinity for mGlu2 and mGlu3(Ki=144nM and 156nM, respectively).
YN320710 LY2979165 1311385-32-6
LY2979165 is the alanine prodrug of 2812223, a selective and potent orthostericmGlu2receptor agonist.
YF-2 is a highly selective, blood-brain-barrier permeablehistone acetyltransferaseactivator, acetylates H3 in the hippocampus, with EC50s of 2.75μM, 29.04μM and 49.31μM for CBP, PCAF, and GCN5, respectively, shows n...
YN310293 YF-2 hydrochloride 1312005-62-1
YF-2 hydrochloride is a highly selective, blood-brain-barrier permeablehistone acetyltransferaseactivator, acetylates H3 in the hippocampus, with EC50s of 2.75μM, 29.04μM and 49.31μM for CBP, PCAF, and GCN5, respect...
YN360472 Ro 25-6981 Maleate 1312991-76-6
Ro 25-6981 Maleate is a potent and selective activity-dependent blocker of NMDA receptors containing the NR2B subunit. IC50 values are 0.009 and 52μM for cloned receptor subunit combinations NR1C/NR2B and NR1C/N...
7-BIA is areceptor-type protein tyrosine phosphatase D (PTPRD)inhibitor with an IC50 of ~1-3μM.
YN321847 Hemopressin (human, mouse) 1314035-51-2
Hemopressin is a nonapeptide derived from the α1-chain of hemoglobin, is originally isolated from rat brain homogenates. Hemopressin is orally active, selective and inverse agonist ofCB1cannabinoid receptors. Hemopressin exerts anti...
YN320322 AZD-8529 mesylate 1314217-69-0
AZD-8529 mesylate is a potent, highly selective and orally bioavailable positive allosteric modulator ofmGluR2, with an EC50 of 285nM, and shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6,...
YN483844 PDZ1 Domain inhibitor pept... 1315378-73-4
PDZ1 Domain inhibitor peptide, a cyclic peptide, incorporates a β-Ala lactam side chain linker and targets the PDZ1 domains of the postsynaptic density protein 95 (PSD-95). PDZ1 Domain inhibitor peptide disrupts the GluR...
YN320418 NPEC-caged-LY379268 1315379-62-4
NPEC-caged-LY379268 is atype II mGluRagonist.
YN320688 Olodanrigan 1316755-16-4
Olodanrigan (EMA401, PD-126055, (S) PD-126055) is a highly selective, orally active, peripherally restricted antagonist of angiotensin II type 2 receptor (AT2R). Olodanrigan (EMA401) analgesic action appears to involve the...
YN360584 (S)-(-)-5-Fluorowillardiine ... 1321546-70-6
(S)-(-)-5-Fluorowillardiine hydrochloride is a potent and specific AMPAR agonist.
YN371541 Nordoxepin D3 hydrochloride 1331665-54-3
Nordoxepin D3 hydrochloride (Desmethyldoxepin D3 hydrochloride) is the deuterium labeled Nordoxepin hydrochloride. Nordoxepin hydrochloride is an active metabolite of Doxepin hydrochloride (HY-B0725), which is an orally active tri...
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