| Cat. No. |
Product Name |
Information |
| PC-42254 |
YL0919
5-HT1A antagonist
|
YL0919 (Hypidone hydrochloride) is an orally active, dual 5-HT1A agonist and selective serotonin reuptake inhibitor with Ki of 0.19 nM and IC50 of 1.78 nM, respectively. |
| PC-45232 |
Iloperidone
|
Iloperidone (HP-873) is an atypical antipsychotic that exhibits high affinity to serotonin 5HT2A (Ki =5.6 nM), dopamine D2 (Ki=6.3 nM) and D3 (Ki=7.1 nM) and noradrenaline α1 receptors (Ki=0.36 nM), moderate affinity for D4 (25 nM), 5HT6 (43 nM), 5HT7 (22 nM), and low affinity for 5HT1A (168 nM), D1 and histamine H1 receptors. |
| PC-22530 |
RE104
5-HT2A agonist
|
RE104 is the prodrug of 4-OH-DiPT, a synthetic 5-hydroxytryptamine 2A receptor (5-HT2A receptor) agonist with Ki of 0.12 uM. |
| PC-22529 |
4-OH-DiPT
5-HT2A agonist
|
4-OH-DiPT is a synthetic 5-hydroxytryptamine 2A receptor (5-HT2A receptor) agonist with Ki of 0.12 uM, shows strongest agonist activity at all three 5-HT2A/2B/2C receptors with near full agonist activity at 5-HT2A. |
| PC-22510 |
DSP-6745
SERT/5-HT inhibitor
|
DSP-6745 is a potent inhibitor of 5-HT transporter (human SERT, Ki=0.653 nM), and 5-HT2A, 5-HT2C, and 5-HT7 receptors with Ki of 0.331, 1.34, and 31.7 nM, respectively. |
| PC-22491 |
XOB
5-HT2A/VGSC antagonist
|
XOB is a selective antagonist of 5-HT2A receptor and voltage-gated sodium channels, simultaneously antagonizes 5-HT2A receptors and blocks sodium voltage-gated sodium channels (VGSCs). |
| PC-22332 |
ITI-333
5-HT2A agonist
|
ITI-333 is a potent, brain-penetrant, orally bioavailable 5-HT2A receptor antagonist (Ki =8 nM) and a biased, partial agonist at μ-opioid (MOP) receptors (Ki =11 nM, lacking β-arrestin agonism). |
| PC-22310 |
S32212
5-HT2C antagonist
|
S32212 is a combined serotonin (5-HT)(2C) receptor inverse agonist and α(2)-adrenoceptor antagonist with pKi of8.2 (h5-HT2C), pKi of 7.2-8.2 for α(2A), α(2B) and α(2C). |
| PC-22278 |
SB 269970 hydrochloride
5-HT7 antagonist
|
SB269970 (SB-269970) hydrochloride is a potent, selective 5-HT7 receptor antagonist with pKi of 8.9, >100-fold selective over other 5-HT receptors. |
| PC-22277 |
SB269970
5-HT7 antagonist
|
SB269970 (SB-269970) is a potent, selective 5-HT7 receptor antagonist with pKi of 8.9, >100-fold selective over other 5-HT receptors. |
| PC-22276 |
DR4004
5-HT7 antagonist
|
DR4004 (DR-4004) is a potent, highly selective 5-HT7 antagonist with bingding pKi of 8.67, >50-fold selectivity over the 5-HT2 receptor, and other 5-HT receptors. |
| PC-22275 |
DR4004 hydrochloride
5-HT7 antagonist
|
DR4004 (DR-4004) hydrochloride is a potent, highly selective 5-HT7 antagonist with bingding pKi of 8.67, >50-fold selectivity over the 5-HT2 receptor, and other 5-HT receptors. |
