Chemical
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- Catálogos PDF
Chemical Hay 28543 productos.
Dotinurad
Dotinurad is a potent selective urate reabsorption inhibitor. Dotinurad inhibits Urate Transporter 1 (URAT1), IC50 value is 37.2 nM. Dotinurad is used as a uric acid-enhancing excretor.
ZL0580
ZL0580 is a structural analogue of ZL0590 that induces epigenetic suppression of HIV by selectively binding to the BRD4 domain of BD1. ZL0580 induces inhibition of HIV by inhibiting Tat transcriptional activation and transcriptional prolongation, as well as inducing inhibition of chromatin structures on an HIV promoter.
Flavokawain B
Flavokawain B (Flavokavain B) is a chalcone isolated from the root extract of kava drunken pepper and is an effective apoptotic inducer that inhibits the growth of various cancer cell lines. (Flavokavain B) has strong anti-angiogenic activity. (Flavokavain B) inhibits the migration and vascular formation of human brain endothelial cells (HUVEC) at very...
ZL0580
ZL0580 is a structural analogue of ZL0590 that induces epigenetic suppression of HIV by selectively binding to the BRD4 domain of BD1. ZL0580 induces inhibition of HIV by inhibiting Tat transcriptional activation and transcriptional prolongation, as well as inducing inhibition of chromatin structures on an HIV promoter.
ZL0580
ZL0580 is a structural analogue of ZL0590 that induces epigenetic suppression of HIV by selectively binding to the BRD4 domain of BD1. ZL0580 induces inhibition of HIV by inhibiting Tat transcriptional activation and transcriptional prolongation, as well as inducing inhibition of chromatin structures on an HIV promoter.
Dextran (Mw 70000)
Dextran (Mw 70000) has an inhibitory effect on platelet aggregation and coagulation factors, and can replace part of the whole blood during blood transfusion, and is often used as a plasma volume expander (plasma replacement).
LY-3475070
Ly-3475070 is the first oral bioavailable, selective and extracellular enzyme CD73 (cluster of Differentiation 73, 5'-ecto-nucleotidase, 5' -nt, Ecto -5'-nucleotidase) inhibitor.
Succinyl phosphonate trisodium salt
Succinyl phosphonate trisodium salt is an inhibitor of α -ketoglutarate dehydrogenase (KGDHC) that effectively inhibits KGDHC in muscle, bacteria, brain, and human fibroblasts. Succinyl phosphonate trisodium salt inhibits 2-oxyglutarate dehydrogenase (OGDH) and damages cancer cell viability in a cell-specific, metabolically dependent manner.
Tauroursodeoxycholate dihydrate
Tauroursodeoxycholate (Tauroursodeoxycholic acid; TDUCA) dihydrate is an endoplasmic reticulum stress inhibitor. Tauroursodeoxycholate significantly reduces the expression of apoptotic molecules such as caspase-3 and caspase-12. Tauroursodeoxycholate also suppresses ERK.
Eclitasertib
Eclitasertib (DNL-758) is a receptor interaction protein kinase 1 (RIPK1) inhibitor, with IC50 value of
NVP-BSK805
NVP-BSK805 is a potent, selective, ATP competitive JAK2 inhibitor with an IC50 of 0.5 nM, which is more than 20 times more selective than acting on JAK1, JAK3 and TYK2.
N-Hexanoyl-L-homoserine lactone
N-hexanoyl-l-homoserine lactone is a short-chain N-acyl-homoserine lactone (AHL). AHL is an intercellular communication signal molecule in the quorum-sensing system of Gram-negative bacteria and mediates information exchange between eukaryotic plants and prokaryotic bacteria.