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Search Results for " cotransporter "

Targets

28

Compounds

5

Natural Products

3

Recombinant Proteins

Cat No. Product Name Synonyms Targets
T2010 S0859 Others
S0859 is an N-cyanosulphonamide that blocks the sodium/bicarbonate cotransporter (NBC, also known as SLC4A7), which regulates intracellular pH.
T38843 Enavogliflozin DWP-16001 SGLT
Enavogliflozin (DWP-16001) is an orally available small molecule and sodium glucose transporter 2 inhibitor.
TQ0011 PF-06869206 Sodium Channel
PF-06869206 is an oral selective inhibitor of the sodium-phosphate cotransporter NaPi2a (SLC34A1, IC50: 380 nM).
T17243 VU0463271 N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide Potassium Channel
VU0463271 (N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide) is a potent and selective antagonist of the neuronal-specific potassium-chloride cotransporter 2 (KCC2), with an IC50 of 61 nM ...
T5444 CLP290 CLP-290 Potassium Channel
CLP290 is an activator of the neuron-specific K+-Cl cotransporter KCC2 and displays potential for the treatment of a wide range of neurological and psychiatric indications.
TQ0139 VU 0240551 N-(4-Methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide,VU0240551-2-D4 Potassium Channel , Calcium Channel , HER
VU 0240551 is a selective antagonist of neuronal K-Cl cotransporter KCC2 inhibitor with an IC50 of 560 nM. VU 0240551 inhibits L-type calcium channels and hERG.
T4999 Ertugliflozin MK-8835,PF-04971729 SGLT
PF-04971729 (Ertugliflozin (PF-04971729)) is a potent and selective inhibitor of the sodium-dependent glucose cotransporter 2 (SGLT2).
T14984 CLP257 Potassium Channel
CLP257 is a selective K+-Cl− cotransporter KCC2 activator (EC50: 616 nM) and it is inactive against NKCC1, GABAA receptors, KCC1, KCC3 or KCC4. CLP257 alleviates hypersensitivity in rats with neuropathic painc and it al...
T4564 Ethacrynic acid Edecrin,Etacrynic Acid,Hydromedin Others , Calcium Channel , NF-κB , GST
Ethacrynic acid (Edecrin) is a nonsulfonamide loop diuretic that inhibits the activity of the Na+/K+/2Cl- cotransporter NKCC2 in the thick ascending limb of the loop of Henle. It also inhibits glutathione S-transferase a...
T35336 Furosemide sodium Frusemide Sodium,Lasix Na-K-Cl cotransporter
Furosemide sodium (Frusemide Sodium) is a potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter, NKCC1 and NKCC2. Furosemide sodium is also a GABAA receptors antagonist and displays 100-fold selectivity ...
T16818 S-8921 Others
S-8921 is an inhibitor of ileal Na+/bile acid cotransporter.
T11528 H100 Others
H100 is a Cl- transport inhibitor, no effect against KCl cotransporter. It has partial effects against both the NaK2Cl cotransporter and the Band 3 anion exchanger.
T17221 Velagliflozin SGLT
Velagliflozin is an orally available inhibitor of sodium-glucose cotransporter 2.
T30534 BMS-639432
BMS-639432 is a potent sodium-glucose cotransporter type II (SGLT2) inhibitor.
T15752 Licogliflozin LIK066 SGLT
Licogliflozin (LIK066) is an inhibitor of sodium-glucose cotransporter (SGLT1 and SGLT2).
T21399 Luseogliflozin TS71,TS-071,TS 71,TS071,TS-71,TS 071
Luseogliflozin, a potent and competitive inhibitor of sodium-dependent glucose cotransporter 2 (SGLT2), competitively inhibits human SGLT2-mediated glucose uptake with a Ki value of 1.10 nM.
T28971 Tianagliflozin
Tianagliflozin, a sodium/glucose cotransporter 2 (SGLT-2) inhibitor, is used potentially for the treatment of type 2 diabetes.
T15797 LX2761 Others
LX2761 is a chemically stable and effective inhibitor against sodium-dependent glucose cotransporter 1 (SGLT1) and SGLT2 (IC50s: 2.2 nM and 2.7nM for hSGLT1 and hSGLT2). However, it shows specific SGLT1 inhibition in the...
T12892 SGL5213 SGLT
SGL5213 is an oral active and low-absorbable inhibitor of sodium-dependent glucose cotransporter 1 (SGLT1)(hSGLT1 and hSGLT2 with IC50 values of 29 nM and 20 nM , respectively),and has potential to treat type 2 diabetes.
T13179 Tofogliflozin CSG452 Others
Tofogliflozin is a highly specific inhibitor of sodium/glucose cotransporter 2 (SGLT2) (Kis: 2.9, 14.9, and 6.4 nM for human, rat, and mouse SGLT2. IC50s: 2.9/14.9/6.4 nM (human/rat/mouse SGLT2)).
T68236 TP0438836
TP0438836 is a potent, low-absorbable sodium-dependent glucose cotransporter 1 (SGLT1) inhibitor for the treatment of type 2 diabetes. TP0438836 showed IC50 values 28nM and 7 nM for hSGLT1 and hSGLT2 resepctively.
T61713 Bumetanide sodium
Bumetanide sodium is a potent loop diuretic that acts as a blocker for the sodium-potassium-chloride cotransporter (NKCC). It selectively inhibits NKCC1 and NKCC2, with IC50 values of 0.68 μM and 4.0 μM for hNKCC1A and h...
T35728 Hydrochlorothiazide Impurity C
Hydrochlorothiazide impurity C is a potential impurity found in commercial hydrochlorothiazide preparations. [1] Hydrochlorothiazide is a thiazide diuretic that inhibits the apical membrane sodium chloride cotransporter ...
T68922 YM543 free base
YM543 free base, a potent and orally active sodium-glucose cotransporter (SGLT) 2 inhibitor, effectively reduces blood glucose levels and is suitable for diabetes research.
T35619 Dapagliflozin-3-O-β-D-Glucuronide
Dapagliflozin-3-O-β-D-glucuronide is a metabolite of dapagliflozin . Dapagliflozin is a first generation selective sodium glucose cotransporter (SGLT) 2 inhibitor that blocks glucose transport.[1] Dapagliflozin is metab...
T70390 YM-543 choline
YM-543, also known as ASP-543, is a selective SGLT2 inhibitor. Sodium-glucose cotransporter 2 (SGLT2) is a specifically expressed transporter in the kidney that plays an important role in renal glucose reabsorption, and ...
T72143 Velagliflozin proline hydrate
Velagliflozin proline hydrate, the clinical form of Velagliflozin, is an oral sodium-glucose cotransporter 2 (SGLT2) inhibitor exhibiting antidiabetic activity. By decreasing renal glucose reabsorption and promoting glyc...
T35876 Chlorthalidone Impurity G
Chlorthalidone impurity G is a potential impurity found in commercial preparations of chlorthalidone that has moderate antihypertensive effects. Chlorthalidone is a thiazide-like diuretic that inhibits the Na+/Cl- cotran...

Compounds

S0859
T2010
Synonym:
Target: Others
Enavogliflozin
T38843
Synonym: DWP-16001
Target: SGLT
PF-06869206
TQ0011
Synonym:
Target: Sodium Channel
VU0463271
T17243
Synonym: N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide
Target: Potassium Channel
CLP290
T5444
Synonym: CLP-290
Target: Potassium Channel
VU 0240551
TQ0139
Synonym: N-(4-Methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide,VU0240551-2-D4
Target: Potassium Channel, Calcium Channel, HER
Ertugliflozin
T4999
Synonym: MK-8835,PF-04971729
Target: SGLT
CLP257
T14984
Synonym:
Target: Potassium Channel
Ethacrynic acid
T4564
Synonym: Edecrin,Etacrynic Acid,Hydromedin
Target: Others, Calcium Channel, NF-κB, GST
Furosemide sodium
T35336
Synonym: Frusemide Sodium,Lasix
Target: Na-K-Cl cotransporter
S-8921
T16818
Synonym:
Target: Others
H100
T11528
Synonym:
Target: Others
Velagliflozin
T17221
Synonym:
Target: SGLT
BMS-639432
T30534
Synonym:
Target:
Licogliflozin
T15752
Synonym: LIK066
Target: SGLT
Luseogliflozin
T21399
Synonym: TS71,TS-071,TS 71,TS071,TS-71,TS 071
Target:
Tianagliflozin
T28971
Synonym:
Target:
LX2761
T15797
Synonym:
Target: Others
SGL5213
T12892
Synonym:
Target: SGLT
Tofogliflozin
T13179
Synonym: CSG452
Target: Others
TP0438836
T68236
Synonym:
Target:
Bumetanide sodium
T61713
Synonym:
Target:
Hydrochlorothiazide Impurity C
T35728
Synonym:
Target:
YM543 free base
T68922
Synonym:
Target:
Dapagliflozin-3-O-β-D-Glucuronide
T35619
Synonym:
Target:
YM-543 choline
T70390
Synonym:
Target:
Velagliflozin proline hydrate
T72143
Synonym:
Target:
Chlorthalidone Impurity G
T35876
Synonym:
Target:
Cat No. Product Name Synonyms Targets
TN1842 Kushenol I GABA Receptor , Antifection
Kushenol I is a GABAA receptor modulator, it exhibits inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2).Kushenol I is shown to be active against the plant pathogenic fungus Cladosporium cucumeri...
TN1847 Kushenol X Others
Kushenol X exhibits inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2).
TN1841 Kushenol A Leachianone E cAMP
Kushenol A is a kind of Adenosine 3', 5'-cyclic monophosphate(cAMP)phosphodiesterase inhibitiors, it shows selective alpha-glucosidase inhibitory activity. Kushenol A and kushenol C exhibit inhibitory activity against So...
TN4399 Kushenol C SGLT , NF-κB , ROS , BACE , Antifection
Kushenol C is a good 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenger, and it exhibits inhibitory activity against Sodium-dependent glucose cotransporter 2(SGLT2). Kushenol C shows antimicrobial activity against Staphyloco...
TN2553 1-Methyl-2-undecyl-4(1H)-quinolone 1-Methyl-2-undecylquinolin-4(1H)-one MAO
1-Methyl-2-undecyl-4(1H)-quinolone, and dihydroevocarpine should also be served as the chemical markers together with evodiamine for the quality control of Evodia rutaecarpa (Juss.) Benth. 1-Methyl-2-undecyl-4(1H)-quinol...

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPH-02124 SLC23A2 Protein, Human, Recombinant (His) Human in vitro E. coli expression system
Sodium/ascorbate cotransporter. Mediates electrogenic uptake of vitamin C, with a stoichiometry of 2 Na(+) for each ascorbate.
TMPH-02119 SLC5A2 Protein, Human, Recombinant (His & Myc) Human E. coli
Sodium-dependent glucose transporter. Has a Na(+) to glucose coupling ratio of 1:1.; Efficient substrate transport in mammalian kidney is provided by the concerted action of a low affinity high capacity and a high affini...
TMPJ-00935 PDIA3 Protein, Human, Recombinant (His) Human Human Cells
PDIA3 protein is also known as Protein disulfide-isomerase A3. It is a protein that in humans is encoded by the PDIA3 gene.PDIA3 is an enzyme that belongs to the endoplasmic reticulum and interacts with lectin chaperones...
TargetMol