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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T5623 | Bisphenol A | Others , Endogenous Metabolite | |
Bisphenol A is an endogenous metabolic compound of phenols and is widely used in the production of epoxy resins and polycarbonate plastics. It is reproductive, developmental and systemic toxicant and is often classified ... | |||
T20396 | Levadopa Related Compound A | 6-Hydroxydopa, L-,L-Hydroxydopa | |
Levadopa Related Compound A is the 6-hydroxy derivative of the amino acid L-DOPA with neurotoxic properties. Exogenously administered 6-Hydroxy-L-DOPA is biotransformed by an amino acid decarboxylase to the highly potent... | |||
T124815 | Barbaloin-related compound A | ||
Barbaloin-related compound A is a useful organic compound for research related to life sciences and the catalog number is T124815. | |||
T67035 | Imiquimod Related Compound A | ||
Imiquimod Related Compound A is a useful organic compound for research related to life sciences. The catalog number is T67035 and the CAS number is 99010-24-9. | |||
T125853 | Clopidogrel Related Compound A | ||
Clopidogrel Related Compound A is a useful organic compound for research related to life sciences. The catalog number is T125853 and the CAS number is 144457-28-3. | |||
T3586 | Compound 401 | 2-morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one | DNA-PK |
Compound 401 (2-morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one) is a synthetic DNA-PK inhibitor (IC50 = 0.28 μM) that also targets mTOR but not PI3K. | |||
T8555 | Neuraminidase-IN-1 | Novel NA Inhibitor,Compound Y-1 | Others , Influenza Virus |
Neuraminidase-IN-1 (Compound Y-1) is a novel neuraminidase inhibitor. | |||
T39578 | TPh A | Triphenyl Compound A | |
Triphenyl Compound A (TPh A) is an effective inhibitor of nuclear protein pirin, showing specific binding to pirin with a Ki value of 0.6 uM. Its mechanism of action involves disturbing the formation of the bcl3–pirin co... | |||
T26817 | Bim-BLK-A | Bim Blocker A,Compound A,Bim BLK A,BimBLKA | |
Bim-BLK-A efficiently blocks Bim-induced apoptosis after Bax is activated on the mitochondria. The cellular target of Bim-BLK-A was identified to be the succinate dehydrogenase subunit B (SDHB) protein of complex II of t... | |||
T70626 | MS 347a | ||
MS 347a is a myosin light chain kinase (MLCK) inhibitor; an epoxide analog of sydowinin B (MS-347b). | |||
T20995 | Amlodipine besilate impurity D | Amlodipine Related Compound A,Amlodipine impurity A | |
Amlodipine besilate impurity D is a biochemical. | |||
T20683 | Letrozole related compound B | Letrozole specified impurity A | |
Letrozole related compound B is an impurity of aromatase inhibitor. | |||
T6146 | Dorsomorphin dihydrochloride | BML-275 2HCl,Compound C dihydrochloride,Dorsomorphin (Compound C) 2HCl,Compound C 2HCl,BML-275 dihydrochloride | AMPK , Autophagy , TGF-beta/Smad |
Dorsomorphin dihydrochloride (BML-275 2HCl) is a potent, selective and ATP-competitive AMPK inhibitor (Ki: 109 nM) and does not exhibit significant activity on structurally related kinases. | |||
T67456 | Argatroban Related Compound A | ||
(2R,4R)-4-Methyl-1-((S)-2-(3-methylquinoline-8-sulfonamido)-5-(3-nitroguanidino)pentanoyl)piperidine-2-carboxylic acid is a useful organic compound for research related to life sciences and the catalog number is T67456. | |||
T24994 | MreB Perturbing Compound A22 hydrochloride | A22 hydrochloride,MreB Perturbing Compound A22 | |
A22 is an inhibitor of MreB, an actin-like bacterial protein, and has been proved to be an antibiotic adjuvant. A22 inhibition of MreB disrupts the bacterial actin cytoskeleton, which can cause an increase in cell permea... | |||
T68808 | 11-Dehydrocorticosterone | ||
11-Dehydrocorticosterone is an endogenous mineralocorticoid. It increases Na+/K+-ATPase mRNA expression in vascular smooth muscle cells and inhibits aldosterone action in B. marinus toad bladder tissue in a concentration... | |||
T25796 | Methotrexate 1-methyl ester | Methotrexate related compound I,Methotrexate alpha-methyl ester | |
Methotrexate 1-methyl ester is an impurity of Methotrexate which is a folic acid antagonist. It's used as an antineoplastic and antirheumatic. | |||
T14119 | ACT-678689 | Compound Example 1.53.4 | Hydroxylase |
ACT-678689 (Compound Example 1.53.4) (Compound Example 1.53.4) is a tryptophan hydroxylase (TPH) inhibitor with an IC50 of 8 nM[1]. | |||
T28662 | Saripidem | SL-850274,SL-85.0274,SL850274,SL85.0274 | Others |
Saripidem (SL-85.0274) is a compound with anxiolytic activity. | |||
T77771 | Compound 10w | Others | |
Compound 10w, a substituted pyrazolo[1,5-a]pyrimidinamide compound, is a ZSTK474 analog that shows anticancer activity against HeLa cells. |