Membrane Transporter/Ion Channel
Membrane Transporter/Ion Channel(跨膜转运)
- AMPAR(58)
- ATPase(80)
- Calcium Channel(331)
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- Glucose Transporters(13)
- Glutamate (EAAT) Transporters(18)
- Glycine Receptors(2)
- GlyT(19)
- GTPase(32)
- Kv1.3(1)
- ICB(2)
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- M2 ion Channel(1)
- MCT2(2)
- Monoamine transporter(18)
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- Na+/Ca2+ Exchanger(16)
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- Nucleoside Transporters(4)
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- MCT(3)
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- Ionophore(3)
- sodium-hydrogen exchanger(3)
- Chloride Channel(27)
- CRAC Channel(13)
- EAAT2(6)
- HCN Channel(6)
- Na+/HCO3- Cotransporter(1)
- Na+/K+ ATPase(28)
- P-glycoprotein(49)
- iGluR(164)
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- Urea Transporter(1)
- Na+/H+ Exchanger (NHE)(1)
- NTPDase(1)
- EAAT(1)
- Piezo Channel(1)
- ASCT(2)
Membrane Transporter/Ion Channel 相关产品(2265)
- GC16981KN-92 phosphateCAS: 1135280-28-2纯度: >99.50%
KN-92 phosphate 是 KN-93 的无活性衍生物,没有 CaM 激酶抑制活性。 KN-92 磷酸盐旨在用作旨在阐明 KN-93 拮抗剂活性的研究中的对照化合物。 KN-93 是一种细胞渗透性、可逆性和竞争性 CaMKII 抑制剂。
- GC17065Estradiol 3-(β-D-Glucuronide) (sodium salt)CAS: 14982-12-8纯度: >95.00%
An isomer of estradiol-(β-D-glucuronide)
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC16924 | Eniporide | 176644-21-6 | - | |
A NHE-1 inhibitor | ||||
| GC16937 | Carbamoylcholine chloride | 51-83-2 | >98.00% / >99.00% | |
Cholinergic receptor agonist | ||||
| GC16942 | GMQ hydrochloride | 5361-15-9 | - | |
An ASIC3 activator | ||||
| GC16945 | Astemizole | 68844-77-9 | >99.50% | |
Astemizole是一种强效抗组胺化合物,可拮抗组胺H1受体,IC 50 值为4nM。 | ||||
| GC16947 | CGP 52432 | 139667-74-6 | >98.00% | |
A GABA B receptor antagonist | ||||
| GC16948 | Valinomycin | 2001-95-8 | >98.00% / >95.00% | |
缬霉素Valinomycin是一种十二肽抗生素,从几种链霉菌菌株中获得。 | ||||
| GC16962 | W-5 hydrochloride | 61714-25-8 | - | |
A low-affinity calmodulin antagonist | ||||
| GC16965 | Zatebradine hydrochloride | 91940-87-3 | >99.00% | |
A bradycardic HCN channel blocker | ||||
| GC16981 | KN-92 phosphate | 1135280-28-2 | >99.50% | |
KN-92 phosphate 是 KN-93 的无活性衍生物,没有 CaM 激酶抑制活性。 KN-92 磷酸盐旨在用作旨在阐明 KN-93 拮抗剂活性的研究中的对照化合物。 KN-93 是一种细胞渗透性、可逆性和竞争性 CaMKII 抑制剂。 | ||||
| GC17001 | Verruculogen | 12771-72-1 | >95.00% | |
A tremorgenic mycotoxin | ||||
| GC17009 | L-trans-2,4-PDC | 64769-66-0 | >98.00% | |
An inhibitor of L-glutamate transport | ||||
| GC17027 | POM 1 | 12141-67-2 | >98.00% | |
POM 1是一种核苷三磷酸二磷酸水解酶(NTPDase)抑制剂,对NTPDase1(CD39)、NTPDase3和NTPDase2的K i 值分别为2.58μM、3.26μM和28.8μM。 | ||||
| GC17065 | Estradiol 3-(β-D-Glucuronide) (sodium salt) | 14982-12-8 | >95.00% | |
An isomer of estradiol-(β-D-glucuronide) | ||||
| GC17069 | pep2m | 243843-42-7 | - | |
GluR2亚基C端与N-乙基马来酰亚胺敏感融合蛋白相互作用的肽抑制剂 | ||||
| GC17086 | Chlorpropamide | 94-20-2 | >99.50% | |
A first generation sulfonylurea | ||||
| GC17091 | A 784168 | 824982-41-4 | - | |
A TRPV1 antagonist | ||||
| GC17103 | Pep1-TGL | - | - | |
Peptide containing the 'TGL' motif that corresponds to the C-terminus of GluR1 subunit | ||||
| GC17127 | Decynium 22 | 977-96-8 | - | |
An inhibitor of monoamine transporters and OCTs | ||||
| GC17163 | Elacridar hydrochloride | 143851-98-3 | >98.00% | |
An inhibitor of MRP-1 and BCRP | ||||
| GC17168 | APETx2 | 713544-47-9 | >95.00% / >98.00% | |
APETx2是一种来自 Anthopleura elegantissima 的肽毒素,是选择性、可逆的酸敏感离子通道3(ASIC3)抑制剂。 | ||||
| GC17206 | DL-AP5 | 76326-31-3 | >95.00% / >98.00% | |
DL-AP5是一种选择性NMDA(N-methyl-D-aspartate)受体拮抗剂的外消旋体。D-AP5是活性的(-)立体异构体,能竞争性地抑制NMDA受体的谷氨酸结合位点(K d =1.4μM),而(+)异构体(L-AP5)则显示出相当低的NMDA受体拮抗剂活性。 | ||||
| GC17213 | (S)-AMPA | 83643-88-3 | >99.00% / >98.50% / >98.00% | |
(S)-AMPA (L-AMPA) 是 AMPA 的活性 S-对映异构体,是一种有效的选择性 AMPA 受体激动剂。 | ||||
| GC17215 | Elacridar | 143664-11-3 | >98.00% | |
An inhibitor of MRP-1 and BCRP | ||||
| GC17223 | 17-PA | 694438-95-4 | - | |
17-PA 是神经类固醇增强和 GABAA 受体直接门控的选择性拮抗剂。 | ||||
