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カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
T4369 | SCH-23390 hydrochloride | R-(+)-SCH23390 hydrochloride | Potassium Channel , Dopamine Receptor , 5-HT Receptor |
SCH-23390 hydrochloride (R-(+)-SCH23390 hydrochloride) is an effective dopamine receptor antagonist, and for the D1(Ki=0.2 nM) and D5(Ki=0.3 nM). | |||
T12865 | SCH-23390 maleate | R-(+)-SCH-23390 maleate | Potassium Channel , Dopamine Receptor , 5-HT Receptor |
T6988 | SKF 38393 hydrochloride | (±)-SKF-38393 hydrochloride,SKF-38393A,SKF38393 HCl | Dopamine Receptor |
SKF 38393 hydrochloride (SKF38393 HCl) is a selective dopamine D1/D5 receptor agonist. | |||
T60835 | SKF83959 | Dopamine Receptor | |
SKF83959, a benzazepine analog, is a selective and potent partial agonist of the dopamine D1 receptor with Ki values of 1.18, 7.56, 920, and 399 nM for rat D1, D5, D2, and D3 receptors, respectively.SKF83959 is a potent ... | |||
T16999 | Tavapadon | PF-6649751,CVL-751 | Dopamine Receptor |
Tavapadon (CVL-751) is an orally active and highly selective dopamine D1/D5 receptor partial agonist. | |||
T22921 | LE 300 | Dopamine Receptor , 5-HT Receptor | |
dopamine D1 receptor antagonist | |||
T23066 | NGD 94-1 | Dopamine Receptor | |
NGD 94-1 is a selective D4 receptor antagonist with an affinity of 3 nM for the D4 receptor and greater than 2 pM for the D1, D2, D3, and D5 receptors.NGD 94-1 can be used in the study of cognitive disorders and other ps... | |||
T31602 | Ecopipam | Sch-39166,UNII-0X748O646K,Sch 39166 | Dopamine Receptor |
Ecopipam (UNII-0X748O646K) is a potent, selective and orally active antagonist of dopamine D1/D5 receptor, with Kis of 1.2 nM and 2.0 nM, respectively. Ecopipam shows more than 40-flod selectivity over D2, D4, 5-HT, and ... | |||
T28167 | NGB 2904 | NGB2904 HCl,NGB-2904,NGB2904 | Others , Dopamine Receptor , 5-HT Receptor |
NGB 2904 is a potent and selective antagonist of dopamine D3 receptor (Ki values are 1.4, 217, 223, 642, > 5000, > 10000 and > 10000 nM for D3, D2, 5-HT2, α1, D4, D1 and D5 receptors respectively). NGB2904 potently antag... | |||
T5397 | A-381393 | Dopamine Receptor | |
A-381393 is a selective and brain penetrate dopamine D4 receptor antagonist (Kis: 1.9/1.5/1.6 nM for human dopamine D4.2/D4.4/D4.7 receptor). | |||
T7834 | ABT-724 | Dopamine Receptor | |
ABT-724 is an agonist of dopamine D4 receptor(EC50: 12.4 nM) | |||
T19342 | Glycerol phenylbutyrate-D5 | HPN-100-D5 | Sigma receptor |
Glycerol phenylbutyrate-D5 is a deuterium-labeled Glycerol phenylbutyrate. Glycerol phenylbutyrate is a sigma-2 (σ2) receptor ligand (pKi: 8.02). | |||
T16893 | SKF-82958 | Chloro-AP,(±)-SKF 82958 | Others |
SKF 82958 is a D1/D5 receptor full agonist. | |||
T16892 | SKF-82958 hydrobromide | (±)-SKF 82958 hydrobromide,Chloro-APB hydrobromide | Others |
SKF-82958 hydrobromide is a D1/D5 receptor full agonist. | |||
T13463L | Dihydrexidine | DAR-0100 | Dopamine Receptor |
Dihydrexidine is a full efficacy D1-like dopamine receptor (D1/D5) agonist (IC50: 10 nM for D1 receptor). It also shows potent antiparkinsonian activity. | |||
T10440 | Azilsartan-d5 | TAK-536 D5 | Others |
Azilsartan (TAK-536) D5 is the deuterium-labeled Azilsartan. Azilsartan is a specific antagonist of the angiotensin II type 1 receptor. | |||
T10558 | Blonanserin D5 | AD-5423 D5 | Others |
Blonanserin D5 is a deuterium-labeled Blonanserin. Blonanserin (AD-5423) is a dopamine D2/5-HT2 receptor antagonist with an atypical antipsychotic effect. | |||
T0074L | Chlorprothixene hydrochloride | NSC 78193,Minithixen,Truxal hydrochloride,NSC 56379,NSC 169899,Minithixen hydrochloride | Dopamine Receptor , 5-HT Receptor , Antibacterial , AChR , Histamine Receptor |
Chlorprothixene hydrochloride (Truxal hydrochloride) brings strong blocking effects by blocking the 5-HT2 D1, D2, D3, histamine H1, muscarinic and alpha1 adrenergic receptors. Chlorprothixene hydrochloride s a typical an... | |||
T6647 | Rotigotine- | Neupro,N-0923,N-0437,SPM 962 | Dopamine Receptor , 5-HT Receptor , Adrenergic Receptor |
Rotigotine (N-0923) is a non-ergot dopamine receptor agonist used in the therapy of Parkinson disease and restless leg syndrome. Administered as a once-daily transdermal patch, Rotigotine has not been associated with ser... | |||
T13076 | Tamoxifen-d5 | ICI 47699-d5,(Z)-Tamoxifen-d5,trans-Tamoxifen-d5 | HSP |
Tamoxifen-d5 is a deuterium labeled Tamoxifen. Tamoxifen is a selective modulator of estrogen receptor (SERM). Tamoxifen is a potent activator of Hsp90 and enhances the Hsp90 molecular chaperone ATPase activity. | |||
TMIH-0486 | Ramelteon-d5 | ||
Ramelteon-d5 is a deuterated compound of Ramelteon. Ramelteon has a CAS number of 196597-26-9. Ramelteon is a Melatonin Receptor Agonist. The mechanism of action of ramelteon is as a Melatonin Receptor Agonist. | |||
T12973 | Solifenacin D5 hydrochloride | Others | |
Solifenacin D5 hydrochloride is a deuterium labeled Solifenacin hydrochloride. Solifenacin hydrochloride is an antagonist of muscarinic receptor(pKis of 7.6, 6.9 and 8.0 for M1, M2 and M3 receptors, respectively). | |||
T67921 | Retinoic acid-d5 | all-trans-Retinoic acid-d5,Isotretinoin-d5,Vitamin A acid-d5,Accutane-d5,ATRA-d5 | Retinoid Receptor |
Retinoic acid-d5 (Vitamin A acid-d5) is the deuterium-labeled form of Retinoic acid. Retinoic acid is a natural RAR receptor agonist with an IC50 of 14 nM for RARα/β/γ and a Kd of 17 nM for PPARβ/δ. Retinoic acid, a meta... | |||
T73823 | DETQ | ||
DETQ, a selective, allosteric, and orally active potentiator of the dopamine D1 receptor (Dopamine Receptor), enhances cAMP production in HEK293 cells expressing the human D1 receptor, achieving an EC50 of 5.8 nM and a K... | |||
TMIH-0235 | Finerenone-d5 | ||
Finerenone-d5 is a deuterated compound of Finerenone. Finerenone has a CAS number of 1050477-31-0. Finerenone is a third-generation, selective, and orally available nonsteroidal mineralocorticoid receptor (MR) antagonist... | |||
T70035 | Tasimelteon-d5 | ||
Tasimelteon-d5 is intended for use as an internal standard for the quantification of tasimelteon by GC- or LC-MS. Tasimelteon is a melatonin (MT) receptor agonist. It selectively binds MT1 and MT2 receptors over a panel ... | |||
T21446 | Rotigotine Hydrochloride | Rotigotine (Hydrochloride),N 0923,N-0924,Rotigotine HCl,N-0923 | Dopamine Receptor , 5-HT Receptor , Adrenergic Receptor |
Rotigotine Hydrochloride (N-0924), a dopamine receptor agonist prefering for D3 receptors over D1 and D2, has effective activity of anti-Parkinsonian. Racemic rotigotine hydrochloride is about 50 times as potent as quinp... | |||
T70313 | Indoxyl Sulfate-d5 potassium salt | ||
Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan. It is formed via sulfation of in... | |||
T23364 | SKF 83959 hydrobromide | Others | |
SKF 83959 hydrobromide is a Dopamine D1-like receptor partial agonist. | |||
T23381 | Spiperone hydrochloride | Others | |
5-HT2A serotonin and selective D2-like dopamine receptor antagonist | |||
T12676 | (Rac)-Rotigotine hydrochloride | Dopamine Receptor | |
(Rac)-Rotigotine hydrochloride is a racemate of Rotigotine. Rotigotine is a full agonist of dopamine receptor, a partial the 5-HT1A receptor agonist. | |||
T22858 | Iloperidone hydrochloride | Others | |
Iloperidone hydrochloride is a D(2)/5-HT(2) receptor antagonist. It is also an atypical antipsychotic for the treatment of schizophrenia symptoms. |