Membrane Transporter/Ion Channel
Research Areas
- AMPAR(55)
- Aquaporins(3)
- Piezo Channels(6)
- ATPase(77)
- Calcium Channel(342)
- Cannabinoid Transporters(6)
- CFTR(49)
- Chloride Channels(12)
- GABA Receptor(191)
- Gardos Channel
- Glucose Transporters(17)
- Glutamate (EAAT) Transporters(18)
- Glycine Receptors(2)
- GlyT(19)
- GTPase(30)
- Kv1.3
- ICB(1)
- Lipophilic platinum complex
- M2 ion Channel
- MCT2(2)
- Monoamine transporter(16)
- Monocarboxylate Transporters(14)
- Multidrug Transporters(4)
- Na+/Ca2+ Exchanger(16)
- NKCC(8)
- NMDA Receptor(77)
- Nucleoside Transporters(5)
- Pannexin-1(2)
- P2X purinergic receptor(69)
- P-gp(10)
- Proton Pump(58)
- Potassium Channel(323)
- Sodium Channel(215)
- TRP Channel(184)
- TRPV1(10)
- URAT1(14)
- Other Channel Modulators(10)
- MCT(3)
- Kainate Receptors(11)
- Ionophore(3)
- sodium-hydrogen exchanger(3)
- Chloride Channel(29)
- CRAC Channel(14)
- EAAT2(6)
- HCN Channel(9)
- Na+/HCO3- Cotransporter(1)
- Na+/K+ ATPase(30)
- P-glycoprotein(55)
- iGluR(171)
- nAChR(110)
- VDAC(3)
- GlyR(1)
- Ferroportin(4)
- Urea Transporter(1)
- Na+/H+ Exchanger (NHE)(2)
- NTPDase(3)
- EAAT(5)
- ASCT(3)
- Apical Sodium-Dependent Bile Acid Transporter(1)
- Sec61(2)
- ATP-binding cassette (ABC) transporters(4)
- SLC39 (Zinc Transporter)(1)
- Sodium Phosphate Cotransporter(1)
Products Related to Membrane Transporter/Ion Channel(2345)
- GC81696Hepcidin antagonist-1CAS: 338965-09-6Purity: >98.00%
Hepcidin antagonist-1 (example 104) is a potent hepcidin (hepcidine) antagonist with an IC 50 <50 μM.
- GC81721IvabradineCAS: 155974-00-8Purity: >99.50%
Ivabradine is a potent and orally active HCN (hyperpolarization-activated cyclic nucleotide-gated) channel blocker that inhibits the cardiac pacemaker current (If).
- GC81722pan-HCN-IN-1CAS: 1334308-63-2Purity: >99.50%
pan-HCN-IN-1 is a potent HCN ion channel inhibitor with IC 50 values of 58 nM, 522 nM, 58 nM, and 58 nM against HCN1, HCN2, HCN3, and HCN4, respectively.
- GC81723SaviprazoleCAS: 121617-11-6Purity: >96.00%
Saviprazole (HOE-731) is a H +,K + -ATPase inhibitor.
- GC81724Pyrimidinone 8CAS: 65004-42-4Purity: >99.50%
Pyrimidinone 8 is a reversible linear non-competitive inhibitor of divalent metal transporter 1 ( DMT1 ), with a K i of 20 μM ( hDMT1 ).
- GC81725TRPV1 antagonist 10CAS: 896584-55-7Purity: >98.50%
TRPV1 antagonist 10 is an orally active and potent TRPV1 antagonist ( IC 50 = 33.06 nM), moderate to weak URAT1 ( IC 50 = 22.51 μM) and GLUT9 (60.25% at 50 μM) inhibitor.
- GC81734UCB1244283CAS: 300587-89-7Purity: >99.50%
UCB1244283 is a synaptic vesicle glycoprotein 2A ( SV2A ) allosteric modulator.
- GC81738URAT1 inhibitor 7CAS: 1632002-28-8Purity: >98.00%
URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor, with an IC 50 of 12 nM.
- GC81764ABC transporter modulator-1CAS: 3093661-22-1Purity: >96.00%
ABC transporter modulator-1 (Compound I-5) is an ABC transporter expression enhancer.
- GC81765ABC transporter modulator-2CAS: 3093663-15-8Purity: >96.00%
ABC transporter modulator-2 (Compound I-200) is a ABC transporter expression modulator.
- GC81766ABC transporter modulator-3CAS: 3093661-88-9Purity: >97.00%
ABCC6 modulator-3 (Compound I-71) is a ABCC6 activator with an EC 50 < 1 μM.
- GC81852Piezo1 agonist 2 hydrochloridePurity: >98.50%
Piezo1 agonist 2 hydrochloride is a blood-brain barrier-permeable Piezo1 agonist and Jedi2 conjugate that utilizes LAT1.
- GC81884(R)-Vanzacaftor-d₄Purity: >98.00%
(R)-Vanzacaftor -d 4 ((R)-VX-121-d 4 ) is the deuterated-labeled (R)-Vanzacaftor.
- GC90919Guanosine 5'-[γ-thio]triphosphate (sodium salt)CAS: 1486471-09-3Purity: >95.00%
ترجمة: عنصر تشابهي لـ GTP مقاوم لعملية التحلل المائي.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC81683 | AM9053 | 157469-21-1 | >98.00% | |
AM9053 is a selective, effective and slowly reversible inhibitor of N-acyl ethanolamine acid amidease ( NAAA ) ( IC 50 = 30 nM). | ||||
| GC81696 | Hepcidin antagonist-1 | 338965-09-6 | >98.00% | |
Hepcidin antagonist-1 (example 104) is a potent hepcidin (hepcidine) antagonist with an IC 50 <50 μM. | ||||
| GC81721 | Ivabradine | 155974-00-8 | >99.50% | |
Ivabradine is a potent and orally active HCN (hyperpolarization-activated cyclic nucleotide-gated) channel blocker that inhibits the cardiac pacemaker current (If). | ||||
| GC81722 | pan-HCN-IN-1 | 1334308-63-2 | >99.50% | |
pan-HCN-IN-1 is a potent HCN ion channel inhibitor with IC 50 values of 58 nM, 522 nM, 58 nM, and 58 nM against HCN1, HCN2, HCN3, and HCN4, respectively. | ||||
| GC81723 | Saviprazole | 121617-11-6 | >96.00% | |
Saviprazole (HOE-731) is a H +,K + -ATPase inhibitor. | ||||
| GC81724 | Pyrimidinone 8 | 65004-42-4 | >99.50% | |
Pyrimidinone 8 is a reversible linear non-competitive inhibitor of divalent metal transporter 1 ( DMT1 ), with a K i of 20 μM ( hDMT1 ). | ||||
| GC81725 | TRPV1 antagonist 10 | 896584-55-7 | >98.50% | |
TRPV1 antagonist 10 is an orally active and potent TRPV1 antagonist ( IC 50 = 33.06 nM), moderate to weak URAT1 ( IC 50 = 22.51 μM) and GLUT9 (60.25% at 50 μM) inhibitor. | ||||
| GC81726 | VUANT1 | 663212-40-6 | >98.50% | |
VUANT1 (VU0183254) is an allosteric antagonist of insect odorant receptor ion channels, which has the activity of inhibiting insect odorant receptor signaling. | ||||
| GC81728 | TTFB | 352560-76-0 | >98.00% | |
TTFB (N-(4-tert-butyl-1,3-thiazol-2-yl)-3-fluorobenzamide) is a selective, non-competitive zinc-activated channel ( ZAC ) antagonist. | ||||
| GC81734 | UCB1244283 | 300587-89-7 | >99.50% | |
UCB1244283 is a synaptic vesicle glycoprotein 2A ( SV2A ) allosteric modulator. | ||||
| GC81738 | URAT1 inhibitor 7 | 1632002-28-8 | >98.00% | |
URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor, with an IC 50 of 12 nM. | ||||
| GC81764 | ABC transporter modulator-1 | 3093661-22-1 | >96.00% | |
ABC transporter modulator-1 (Compound I-5) is an ABC transporter expression enhancer. | ||||
| GC81765 | ABC transporter modulator-2 | 3093663-15-8 | >96.00% | |
ABC transporter modulator-2 (Compound I-200) is a ABC transporter expression modulator. | ||||
| GC81766 | ABC transporter modulator-3 | 3093661-88-9 | >97.00% | |
ABCC6 modulator-3 (Compound I-71) is a ABCC6 activator with an EC 50 < 1 μM. | ||||
| GC81824 | (+)-Talinolol | 71369-60-3 | >99.00% | |
(+)-Talinolol is an isomer of Talinolol. | ||||
| GC81838 | ICA604025 | - | >98% | |
ICA604025 is a state-dependent inhibitor of human Nav1.9 voltage-gated sodium channel. | ||||
| GC81852 | Piezo1 agonist 2 hydrochloride | - | >98.50% | |
Piezo1 agonist 2 hydrochloride is a blood-brain barrier-permeable Piezo1 agonist and Jedi2 conjugate that utilizes LAT1. | ||||
| GC81884 | (R)-Vanzacaftor-d₄ | - | >98.00% | |
(R)-Vanzacaftor -d 4 ((R)-VX-121-d 4 ) is the deuterated-labeled (R)-Vanzacaftor. | ||||
| GC90516 | VK-II-86 | 955371-84-3 | >90.00% | |
مثبط لـ SOICR | ||||
| GC90815 | 2',3'-cyclic NADP+ (sodium salt) | 100929-77-9 | >95.00% | |
مادة أساسية لـ CNP | ||||
| GC90867 | 8-bromo NAD+ (sodium salt) | 2022926-16-3 | >95.00% | |
صيغة برو-دواء لـ 8-bromo-cADPR | ||||
| GC90919 | Guanosine 5'-[γ-thio]triphosphate (sodium salt) | 1486471-09-3 | >95.00% | |
ترجمة: عنصر تشابهي لـ GTP مقاوم لعملية التحلل المائي. | ||||
| GC91153 | Sulfonadyn-47 | - | >98.00% | |
مثبط داينامين | ||||
| GC91590 | DTPD-Q | 252950-56-4 | >98.00% | |
DTPD-Q is an oxidized derivative of the antioxidant and methylphenyl substituted p-phenylenediamine DTPD. | ||||
