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首页-小分子抑制剂&激动剂-Immunology/Inflammation-Nitric Oxide Synthase (NOS)

Request The Product List ofNitric Oxide Synthase (NOS) Nitric Oxide Synthase (NOS)

Cat. No. Product Name Information
PC-62229

iNOS inhibitor 12

iNOS inhibitor

iNOS inhibitor 12 is a potent, highly selective iNOS inhibitor with IC50 of 79 nM, dispalys almost 100-fold selectivity over eNOS and nNOS.
PC-61062

nNOS-IN-25

nNOS inhibitor

nNOS-IN-25 is a potent, selective cell permeable neuronal nitric oxide synthase (nNOS) inhibitor with Ki of 30 nM.
PC-60993

ASP9853

iNOS inhibitor

ASP9853 is a potent, orally active iNOS inhibitor (IC50=10 nM, NO release DLD-1 cells) that prevents dimerization of iNOS, but has no effect on the expression or enzyme activity of iNOS.
PC-70228

1400W dihydrochloride

iNOS inhibitor

1400W dihydrochloride is a potent, selective inhibitor of iNOS with Ki of 7 nM.
PC-45544

L-NAME hydrochloride

NOS inhibitor

L-NAME hydrochloride is a widely used inhibitor of NO synthase (NOS) with IC50 of 70 uM for purified brain NOS.
PC-42163

IC-87201

PSD-95/nNOS inhibitor

IC-87201 (IC87201) is a small molecule inhibitor of PSD-95/nNOS interaction with IC50 of 31 uM, without inhibiting nNOS catalytic activity.
PC-42162

ZL006

PSD-95/nNOS inhibitor

ZL006 (ZL 006, ZL006) is a brain penetrant small molecule inhibitor of PSD-95/nNOS interaction that prevents glutamate-induced excitotoxicity and cerebral ischemic damage in vivo.
PC-22301

Cindunistat hydrochloride maleate

iNOS inhibitor

Cindunistat hydrochloride maleate (PHA-84250, SC-084250, PF-00572986, SD-6010) is a potent, selective and orally active inducible nitric-oxide synthase (iNOS) inhibitor.
PC-22300

Cindunistat

iNOS inhibitor

Cindunistat (PHA-84250, SC-084250, PF-00572986, SD-6010) is a potent, selective and orally active inducible nitric-oxide synthase (iNOS) inhibitor.
PC-20973

nNOS inhibitor 17

nNOS inhibitor

nNOS inhibitor 17 is a potent, selective neuronal nitric oxide synthase (nNOS) inhibitor with Ki of 15 and 19 nM for rat and human nNOS, respectively.

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