About 9 results found for searched term "71-30-7" (0.125 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M7391 | TC-S 7006 | MAPKAPK2/MAP3K/MAP4K |
| TC-S 7006 is a potent and selective Tpl2 (Cot; MAP3K8) inhibitor. | ||
| M19354 | Cytosine | Others |
| Cytosine is one of the four major bases found in DNA and RNA. cytosine modifications exhibit circadian oscillations associated with epigenetic diversity and aging. | ||
| M31179 | 12-HETE | Apoptosis |
| 12-HETE is a metabolite of arachidonic acid catalyzed by lipoxygenase (12-LOX). It is also a highly selective ligand that can be used to label mu opioid receptors in membrane and tissue sections. In addition, 12-HETE functions as an inhibitor of apoptosis. | ||
| M41017 | Kazusamycin B | Antibiotic |
| Kazusamycin B is an antibiotic that could be isolated from the fermentation broth of Streptomyces sp. | ||
| M11056 | NSC 617145 | DNA/RNA Synthesis |
| NSC 617145 is a selective werner syndrome helicase (WRN) helicase inhibitor,IC50 The value is 230 nM. NSC 617145 inhibit WRN ATPase and induce double-strand rupture (DSB) and chromosomal abnormalities. NSC 617145 is selective to WRN and superior to BLM, FANCJ, ChlR1, RecQ, and UvrD helicases. | ||
| M28252 | GSK837149A | FAS |
| GSK837149A is a selective inhibitor of human Fatty Acid Synthase (FASN) targeting the KR domain. GSK837149A has reversible inhibition effect on FASN and selectivity for type I FASN (Ki=30 nM). GSK837149A is also a competitive inhibitor of NADPH and a non-competitive inhibitor of acetoacetyl-CoA. GSK837149A can be used for the research of obesity and breast cancer. | ||
| M28287 | LY3020371 hydrochloride | GluR |
| LY3020371 hydrochloride is a potent, selective metabotropic glutamate 2/3 receptor (mGlu2/3) antagonist with Ki of 5.3 and 2.5 nM, potently blocks cAMP formation with IC50 of 16.2 nM. LY3020371 hydrochloride exerts an antidepressant-like signature in vivo. | ||
| M28288 | LY3020371 | GluR |
| LY3020371 is a potent and selective antagonist of glutamate (mGlu) 2/3 receptor, with Kis of 5.26 and 2.50 nM for hmGluR2 and hmGluR3, respectively. LY3020371 can be used for the research of depression. | ||
| M30391 | CAY10471 | Prostaglandin Receptor |
| TM30089 | ||
| CAY10471 (TM30089) is a potent, selective, and orally active prostaglandin D2 receptor CRTH2 antagonist. CAY10471 attenuates the progression of tubulointerstitial fibrosis and chronic contact hypersensitivity (CHS) in animal model. | ||
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