6 products were found matching "Cay13715"!
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CAY10621
Item number: Cay13371-5
CAY10621 is an inhibitor of sphingosine kinase 1 (SPHK1, IC50 = 3.3 µM). It is selective for SPHK1 over SPHK2 at 10 µM and PKC at concentrations less than 100 µM. CAY10621 inhibits SPHK1 activity by 70% in U937 cells when used at a concentration of 5 µM.Formal Name:...
| Keywords: | SKI 5C, SPHK1 Inhibitor 5C, (4S)-2,2-dimethyl-4-(1-oxo-2-hexadecyn-1-yl)-3-oxazolidinecarboxylic acid, 1,1-dimethylethyl... |
| Application: | SPHK 1 inhibitor |
| CAS | 120005-55-2 |
| MW: | 435.6 D |
From 38.00€
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15(R)-Prostaglandin E1
Item number: Cay13710-5
15(R)-PGE1 is the "unnatural" C-15 stereoisomer of PGE1. It is essentially inactive biologically when compared to PGE1. It is a non-competitive inhibitor of 15-hydroxy PGDH with an IC50 of 189 µM.Formal Name: 9-oxo-11alpha,15R-dihydroxy-prost-13E-en-1-oic acid. CAS Number: 20897-91-0. Synonyms: 15(R)-PGE1, 15-epi...
| Keywords: | 15(R)-PGE1, 15-epi PGE1, 9-oxo-11alpha,15R-dihydroxy-prost-13E-en-1-oic acid |
| Application: | PGDH inhibitor |
| CAS | 20897-91-0 |
| MW: | 354.5 D |
From 97.00€
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TAK-242
Item number: Cay13871-5
TAK-242 is an antagonist of toll-like receptor 4 (TLR4) with an IC50 value of 0.68 µM in a secreted alkaline phosphatase (SEAP) assay. It selectively binds to TLR4 over TLR1-3 and TLR5-10 when used at a concentration of 100 nM. TAK-242 (1 µM) prevents the interaction of TLR4 with its adaptor proteins TIRAP or TRAM...
| Keywords: | Resatorvid, 6R-[[(2-chloro-4-fluorophenyl)amino]sulfonyl]-1-cyclohexene-1-carboxylic acid, ethyl ester |
| Application: | TLR4 adaptor binding inhibitor |
| CAS | 243984-11-4 |
| MW: | 361.8 D |
From 98.00€
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Butaprost (free acid)
Item number: Cay13741-5
Butaprost is an EP2 selective agonist which has frequently been used to pharmacologically define the EP receptor expression profile of various human and animal tissues and cells. Prostaglandin free acids generally bind to their cognate receptors with 10 to 100 times the affinity of the corresponding ester...
| Keywords: | (±)-15-deoxy-16S-hydroxy-17-cyclobutyl PGE1, 15-deoxy-16S-hydroxy-17-cyclobutyl PGE1,... |
| Application: | EP2 receptor agonist |
| CAS | 433219-55-7 |
| MW: | 394.6 D |
From 142.00€
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ZLJ-6
Item number: Cay13271-5
ZLJ-6 is a dual inhibitor of COX and 5-lipoxygenase (5-LO) (IC50 = 0.73, 0.31, and 0.99 µM for COX-1, COX-2, and 5-LO, respectively, in whole blood). It reduces carrageenin-induced paw edema (inflammation) in rats and acetic acid-induced abdominal constriction (pain) in mice without causing gastrointestinal ulcers,...
| Keywords: | (5Z)-2-amino-1,5-dihydro-1-methyl-5-[[4-(methylsulfonyl)phenyl]methylene]-4H-imidazol-4-one, monomethanesulfonate |
| Application: | COX inhibitor, 5-LO inhibitor |
| CAS | 1051931-39-5 |
| MW: | 375.4 D |
From 53.00€
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Wortmannin-Rapamycin Conjugate
Item number: Cay13671-5
Phosphoinositide 3-kinase (PI3K) and mammalian target of rapamycin (mTOR) act synergistically in promoting cancer. Wortmannin is a potent inhibitor of PI3K enzymes, while rapamycin blocks mTOR Complex 1 TORC1. Wortmannin-rapamycin conjugate consists of analogs of 17-hydroxy wortmannin and rapamycin conjugated via a...
| Keywords: | 1-(4S,4aR,5R,6aS,7S,9aR,E)-1-(((3-(dimethylamino)propyl)(methyl)amino)methylene)-7,11-dihydroxy-4-(methoxymethyl)-4a,6a-di... |
| Application: | PI3K/TORC1 inhibitors |
| CAS | 1067892-47-0 |
| MW: | 1598.9 D |
From 204.00€
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