Neuroscience
Neuroscience(神经科学)
Neuroscience
Neurons communicate with each other, effector organs and sensory organs through the neurotransmitter – receptor pathway at synapses. Neurotransmitters can be divided into 4 major groups: 1. Amino acids (glumate, aspartate, serine, glycine and GABA); 2. Monoamines (norepinephrine, epinephrine, dopamine, histamine, and serotonin); 3. Peptides (opioid peptides, substance P, somatostatin); and 4. Others (acetylcholine, NO, nucleosides). read more
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Neuroscience 相关产品(3932)
- GC13281VU 0364770CAS: 61350-00-3纯度: >99.50%
An mGluR4 and mGluR6 positive allosteric modulator and mGluR5 antagonist
- GC13361Flavoxate hydrochlorideCAS: 3717-88-2纯度: >99.50%
An internal standard for the quantification of flavoxate
- GC13422NabumetoneCAS: 42924-53-8纯度: >99.50%
An NSAID and a prodrug form of 6-methoxy naphthalene acetic acid
- GC13618TarafenacinCAS: 385367-47-5
Tarafenacin(SVT-40776) 是一种高度选择性的 M3 毒蕈碱受体拮抗剂 (Ki= 0.19 nM),选择性比 M2 受体高约 200 倍。
- GC13625Pramipexole dihydrochlorideCAS: 104632-25-9纯度: >99.50%
A dopamine D 2S , D 2L , D 3 , and D 4 receptor agonist
- GC13779Orphenadrine CitrateCAS: 4682-36-4纯度: >98.00%
Orphenadrine citrate 是一种具有口服活性且非竞争性的 NMDA 受体拮抗剂(穿过血脑屏障),Ki 为 6.0 μM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13161 | Escitalopram | 128196-01-0 | - | |
Escitalopram是一种高选择性的5-羟色胺再摄取抑制剂(K i =0.89nM)。 | ||||
| GC13281 | VU 0364770 | 61350-00-3 | >99.50% | |
An mGluR4 and mGluR6 positive allosteric modulator and mGluR5 antagonist | ||||
| GC13300 | Triflusal | 322-79-2 | >99.50% | |
An inhibitor of platelet aggregation | ||||
| GC13322 | Vanoxerine | 67469-69-6 | - | |
Vanoxerine (GBR-12909) 是一种竞争性、强效和高度选择性的多巴胺再摄取抑制剂 (Ki=1 nM)。 | ||||
| GC13339 | Ketoprofen | 22071-15-4 | >99.50% | |
A non-selective COX inhibitor | ||||
| GC13341 | Brompheniramine hydrogen maleate | 980-71-2 | >99.50% | |
A histamine H 1 receptor antagonist | ||||
| GC13361 | Flavoxate hydrochloride | 3717-88-2 | >99.50% | |
An internal standard for the quantification of flavoxate | ||||
| GC13422 | Nabumetone | 42924-53-8 | >99.50% | |
An NSAID and a prodrug form of 6-methoxy naphthalene acetic acid | ||||
| GC13428 | Mosapride | 112885-41-3 | - | |
A 5-HT 4 receptor agonist | ||||
| GC13449 | Rocuronium Bromide | 119302-91-9 | >98.00% | |
A non-depolarizing muscle relaxant | ||||
| GC13478 | Pizotifen Malate | 5189-11-7 | - | |
A triptan | ||||
| GC13486 | Cimetidine | 51481-61-9 | >98.00% | |
A histamine H 2 receptor antagonist | ||||
| GC13501 | VUF 10166 | 155584-74-0 | - | |
A 5-HT 3 receptor antagonist | ||||
| GC13533 | Cisapride | 81098-60-4 | >99.50% | |
A 5-HT 4 receptor agonist | ||||
| GC13569 | Flunixin Meglumin | 42461-84-7 | >99.50% | |
A COX inhibitor | ||||
| GC13572 | Lornoxicam | 70374-39-9 | >99.50% | |
A COX inhibitor and NSAID | ||||
| GC13618 | Tarafenacin | 385367-47-5 | - | |
Tarafenacin(SVT-40776) 是一种高度选择性的 M3 毒蕈碱受体拮抗剂 (Ki= 0.19 nM),选择性比 M2 受体高约 200 倍。 | ||||
| GC13625 | Pramipexole dihydrochloride | 104632-25-9 | >99.50% | |
A dopamine D 2S , D 2L , D 3 , and D 4 receptor agonist | ||||
| GC13626 | Zaltoprofen | 74711-43-6 | >99.50% | |
A non-selective COX inhibitor | ||||
| GC13627 | Ziprasidone hydrochloride monohydrate | 138982-67-9 | >99.50% | |
An atypical antipsychotic | ||||
| GC13654 | Alosetron | 122852-42-0 | - | |
A 5-HT 3 receptor antagonist | ||||
| GC13705 | BMS-927711 | 1289023-67-1 | >99.00% | |
A CGRP receptor antagonist | ||||
| GC13723 | Amitriptyline HCl | 549-18-8 | >99.50% | |
A tricyclic antidepressant | ||||
| GC13779 | Orphenadrine Citrate | 4682-36-4 | >98.00% | |
Orphenadrine citrate 是一种具有口服活性且非竞争性的 NMDA 受体拮抗剂(穿过血脑屏障),Ki 为 6.0 μM。 | ||||
