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5-hydroxymethyl tolterodine (PNU 200577)
Catalog No. A11166 muscarinic receptor 拮抗剂5-hydroxymethyl tolterodine (PNU 200577)是托特罗定的代谢产物，tolterodine是一种用于治疗尿失禁的毒蕈碱受体拮抗剂。 了解更多 -
Biperiden HCl
Catalog No. A10147 -
Tolterodine tartrate (Detrol LA)
Catalog No. A10937 -
Solifenacin succinate
Catalog No. A11215 muscarinic M3 receptor antagoinstSolifenacin succinate是毒蕈碱M3受体拮抗剂，用于治疗尿失禁。 了解更多 -
SVT-40776 (Tarafenacin)
Catalog No. A10808 -
Memantine hydrochloride
Catalog No. A11708 NMDA receptor 拮抗剂Memantine hydrochloride是nmda受体的拮抗剂，与离子通道位点结合。它还是CYP2B6和CYP2D6抑制剂，作用于重组CYP2B6和CYP2D6，Ki分别为0.51 nM和94.9 μM。它被用于治疗帕金森综合征。 了解更多 -
Orphenadrine citrate
Catalog No. A11712 -
TCN 201
Catalog No. A11947 -
SDZ 220-581
Catalog No. A12426 -
A-317491 sodium salt hydrate
Catalog No. A12412 P2X3 and P2X2/3 receptor 拮抗剂A-317491 sodium salt hydrate是一种非核苷酸的P2X3和P2X2/3受体拮抗剂，可抑制受体介导的钙通量。 了解更多 -
Tropisetron HCL
Catalog No. A14375 5-HT3 receptor 拮抗剂Tropisetron HCL是选择性的5-HT3受体拮抗剂和α7烟碱样受体激动剂，对5-HT3受体的IC50为70.1±0.9 nM。 了解更多 -
PF-3635659
Catalog No. A13548 -
(-)-MK 801 maleate
Catalog No. A13435 NMDA receptor 拮抗剂.(-)-MK 801 maleate是一种有效的、选择性的、非竞争性的NMDA受体拮抗剂。它通过与NMDA相关离子通道内的一个位点结合而起作用。 了解更多 -
A 438079 hydrochloride
Catalog No. A14983 P2X7 receptor 拮抗剂A 438079 hydrochloride是一种竞争性P2X7受体拮抗剂（抑制人重组P2X7细胞系中Ca2+流入的pIC50 = 6.9）。 了解更多 -
SDZ 220-581 Ammonium salt
Catalog No. A15235 -
Umeclidinium bromide
Catalog No. A15268 Muscarinic receptor 拮抗剂Umeclidinium bromide (GSK573719A)是毒蕈碱受体拮抗剂，可用于治疗慢性阻塞性肺疾病（COPD）。 了解更多 -
L-701324
Catalog No. A15522 -
(+)-MK 801 Maleate
Catalog No. A12761 -
AZD1283
Catalog No. A15443 -
Revefenacin
Catalog No. A15986 -
Picrotoxin
Catalog No. A14004 GABAA receptor 拮抗剂Picrotoxin是GABAA受体拮抗剂。该化合物已显示可增加下丘脑的去甲肾上腺素水平和周转率。 了解更多 -
A-438079 HCl
Catalog No. A12597 P2X7 receptor 拮抗剂A-438079 HCl是一种竞争性P2X7受体拮抗剂（抑制人重组P2X7细胞系中Ca2+流入的pIC50 = 6.9）。在其他P2受体上没有活性（IC50 > 10 uM）。 了解更多 -
(-)-Securinine
Catalog No. A17102 GABA receptor 拮抗剂(-)-Securinine是一种最初从S. suffructicosa分离的生物碱。Securinine是一种特定的GABA受体拮抗剂，已发现在体内具有显着的CNS活性。 了解更多 -
Atropine methyl bromide
Catalog No. A18026 mAChR antagonistAtropine methyl bromide, a muscarinic receptor (mAChR) antagonist, is a quaternary ammonium salt of atropine and a mydriatic for dilation of the pupil during ophthalmic examination. It is introduced for relieving pyloric spasm in infants for its highly polar nature. It penetrates less readily into the central nervous system than atropine. 了解更多 -
mAChR-IN-1 hydrochloride
Catalog No. A21398 mAChR antagonistmAChR-IN-1 hydrochloride is a potent muscarinic cholinergic receptor (mAChR) antagonist, with an IC50 of 17 nM. 了解更多 -
mAChR-IN-1
Catalog No. A21518 mAChR antagonistmAChR-IN-1 is a potent muscarinic cholinergic receptor(mAChR) antagonist with IC50 of 17 nM. 了解更多 -
Mephenesin
Catalog No. A17493 NMDA receptor antagonistMephenesin is an NMDA receptor antagonist, is a centrally acting muscle relaxant. 了解更多 -
Tiotropium Bromide
Catalog No. A10934 muscarinic acetylcholine receptor (mAChR) antagonistTiotropium Bromide (BA679 BR) is a muscarinic acetylcholine receptor (mAChR) antagonist that blocks the binding of the acetylcholine ligand and subsequent opening of the ligand-gated ion channel. 了解更多 -
GV-196771A
Catalog No. A13438 NMDA receptor antagonistGV-196771A is the sodium salt form of GV196771, is an NMDA receptor antagonist. 了解更多 -
Ifenprodil tartrate
Catalog No. A16583 NMDA receptor antagonistIfenprodil tartrate is the atypical N-methyl-D-aspartate (NMDA) receptor antagonist, inhibits NMDA-induced currents at NR1A/NR2B receptors with high affinity (IC50 = 0.34 μM). 了解更多 -
Transcrocetinate disodium
Catalog No. A21051 NMDA receptor antagonistTranscrocetinate disodium, extracted from saffron (Crocus sativus L.), acts as an NMDA receptor antagonist with high affinity. 了解更多 -
CE-224535
Catalog No. A21183 -
MDL 105519
Catalog No. A21192 NMDA receptor antagonistMDL 105519 is a potent and selective antagonist of glycine binding to the NMDA receptor. 了解更多 -
7-Chlorokynurenic acid sodium salt
Catalog No. A21879 NMDA receptor antagonist7-Chlorokynurenic acid sodium salt is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 了解更多
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