S2698 |
RS-127445 |
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. |
Selective |
5-HT2B, pIC50: 10.4; 5-HT2B, pKi: 9.5 |
S2232 |
Ketanserin |
Ketanserin is a specific 5-HT2A serotonin receptor antagonist with Ki of 2.5 nM for rat and human 5-HT2A, used as an antihypertensive drug. |
Selective |
5-HT2C (Human), Ki: 100 nM; 5-HT2C (Rat), Ki: 50 nM; 5-HT2A, Ki: 2.5 nM |
S8010 |
PRX-08066 Maleic acid |
PRX-08066 Maleic acid is a selective 5-HT2B receptor antagonist with IC50 of 3.4 nM, prevents the severity of pulmonary arterial hypertension in the MCT rat model. Phase 2. |
Selective |
5-HT2B, IC50: 3.4 nM |
S2112 |
Blonanserin |
Blonanserin is a novel atypical antipsychotic agent with potent dopamine D2 (Ki, 14.8 nM) and serotonin 5-HT2(Ki, 3.98 nM) receptors antagonist properties. |
Selective |
5-HT2, Ki: 3.98 nM |
S4086 |
Loxapine Succinate |
Loxapine Succinate is a D2DR and D4DR inhibitor, serotonergic receptor antagonist and also a dibenzoxazepine anti-psychotic agent. |
Selective |
5-HT2 (bovine), Ki: 6.6 nM; 5-HT2 (bovine), Ki: 6.8 nM; 5-HT2 (human), Ki: 6.2 nM |
S2459 |
Clozapine |
Clozapine is an atypical antipsychotic drug by acting as a 5-HT antagonist, used in the treatment of schizophrenia. |
Selective |
|
S2493 |
Olanzapine |
Olanzapine is a high affinity for 5-HT2 serotonin and D2 dopamine receptor antagonist. |
Selective |
|
S1243 |
Agomelatine |
Agomelatine is classified as a norepinephrine-dopamine disinhibitor (NDDI) due to its antagonism of the 5-HT2C receptor. |
Selective |
|
S1283 |
Asenapine |
Asenapine is a high-affinity antagonist of serotonin, norepinephrine, dopamine and histamine receptors, used for the treatment of schizophrenia and acute mania associated with bipolar disorder. |
Pan |
5-HT2C, pKi: 10.46; 5-HT2B, pKi: 9.75; 5-HT2A, pKi: 10.15 |
S1615 |
Risperidone |
Risperidone is a mutil-targeted antagonist for dopamine, serotonin, adrenergic and histamine receptors, used to treat schizophrenia and bipolar disorder. |
Pan |
5-HT2C, Ki: 12 nM; 5-HT2B, Ki: 61.9 nM; 5-HT2A, Ki: 0.17 nM |
S4064 |
Escitalopram Oxalate |
Escitalopram Oxalate is a selective serotonin (5-HT) reuptake inhibitor (SSRI) with Ki of 0.89 nM. |
Pan |
5-HT, Ki: 0.89 nM |
S2663 |
WAY-100635 Maleate |
WAY-100635 Maleate is a potent and selective 5-HT1A receptor agonist with pIC50 of 8.87, exhibits >100-fold selectivity against other 5-HT receptor subtypes and major neurotransmitter receptors. |
Pan |
5-HT, IC50: 0.95 nM |
S4053 |
Sertraline HCl |
Sertraline HCl is a 5-HT antagonist with Ki of 13 nM. |
Pan |
5-HT, Ki: 13 nM |
S2677 |
BRL-15572 |
BRL-15572 is a 5-HT1D receptor antagonist with pKi of 7.9, also shows a considerable affinity at 5-HT1A and 5-HT2B receptors, exhibiting 60-fold selectivity over 5-HT1B receptor. |
Pan |
5-HT2B, pKi: 7.4; 5-HT2C, pKi: 6.2; 5-HT2A, pKi: 6.6 |
S4113 |
Desvenlafaxine |
Desvenlafaxine is a serotonin (5-HT) and norepinephrine (NE) reuptake inhibitor with Ki of 40.2 nM and 558.4 nM, respectively. |
Pan |
5-HT, Ki: 40.2 nM |
S4112 |
Desvenlafaxine Succinate |
Desvenlafaxine Succinate is a new serotonin (5-HT) transporter and norepinephrine (NE) transporter reuptake inhibitor with Ki of 40.2 nM and 558.4 nM respectively. |
Pan |
5-HT, Ki: 40.2 nM |
S3175 |
Atomoxetine HCl |
Atomoxetine is a selective norepinephrine (NE) transporter inhibitor with Ki of 5 nM, with 15- and 290-fold lower affinity for human 5-HT and DA transporters. |
Pan |
5-HT, Ki: 77 nM |
S3183 |
Amitriptyline HCl |
Amitriptyline inhibits serotonin receptor, norepinephrine receptor, 5-HT4, 5-HT2 and sigma 1 receptor with IC50 of 3.45 nM, 13.3 nM, 7.31 nM, 235 nM and 287 nM, respectively. |
Pan |
5-HT2, IC50: 235 nM |
S2691 |
BMY 7378 |
BMY 7378 is a multi-targeted inhibitor of α2C-adrenoceptor and α1D-adrenoceptor with pKi of 6.54 and 8.2, respectively, and acts as a mixed agonist and antagonist for 5-HT1A receptor with pKi of 8.3. |
Pan |
5-HT2, pIC50: 5.5 |
S1333 |
Fluoxetine HCl |
Fluoxetine is a selective serotonin-reuptake inhibitor (SSRI) at the neuronal membrane, used in the treatment of depression. |
Pan |
|
S1336 |
Fluvoxamine maleate |
Fluvoxamine maleate is a selective serotonin (5-HT) reuptake inhibitor (SSRI). |
Pan |
|
S1869 |
Dapoxetine HCl |
Dapoxetine HCl is a short-acting novel selective serotonin reuptake inhibitor. |
Pan |
|
S1432 |
Sumatriptan Succinate |
Sumatriptan Succinate is a triptan sulfa drug containing a sulfonamide group for the treatment of migraine headaches. |
Pan |
|
S2084 |
Duloxetine HCl |
Duloxetine HCl is a serotonin-norepinephrine reuptake inhibitor with Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD). |
Pan |
|
S1245 |
Latrepirdine |
Latrepirdine is an orally active,and neuroactive antagonist of multiple drug targets, including histamine receptors, GluR, and 5-HT receptors, used as an antihistamine drug. |
Pan |
|
S2016 |
Mirtazapine |
Mirtazapine is a potent tetracyclic antidepressant. |
Pan |
|
S3005 |
Paroxetine HCl |
Paroxetine HCl is an antidepressant drug of the SSRI type. |
Pan |
|
S2582 |
Trazodone HCl |
Trazodone HCl is an antidepressant belonging to the class of serotonin receptor antagonists and reuptake inhibitors for treatment of anxiety disorders. |
Pan |
|
S1441 |
Venlafaxine |
Venlafaxine is an arylalkanolamine serotonin-norepinephrine reuptake inhibitor (SNRI), used to treat major depressive disorder (MDD), generalised anxiety disorder (GAD), panic disorder and social phobia. |
Pan |
|
S1483 |
Iloperidone |
Iloperidone is an atypical antipsychotic for the treatment of schizophrenia. |
Pan |
|
S4244 |
Serotonin HCl |
Serotonin HCl is a monoamine neurotransmitter and Endogenous 5-HT receptor agonist. |
Pan |
|
S1649 |
Zolmitriptan |
Zolmitriptan is a selective serotonin receptor agonist. |
Pan |
|
S1488 |
Naratriptan |
Naratriptan is a triptan agent that is used for the treatment of migraine headaches. |
Pan |
|
S2541 |
Clomipramine HCl |
Clomipramine HCl is a hydrochloride salt of clomipramine which is a serotonin transporter (SERT), norepinephrine transporter (NET) dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively. |
Pan |
|