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カタログ番号 | 製品名 | 別名 | ターゲット |
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T19277 | Dexamethasone 9,11-epoxide | Others | |
Dexamethasone 9,11-epoxide is a compound obtained by extraction and is an intermediate in the preparation of dexamethasone. | |||
T37149 | Carbamazepine 10,11-epoxide | Others | |
Carbamazepine 10,11-epoxide is an active metabolite of the anticonvulsant carbamazepine.1,2It is formed from carbamazepine by the cytochrome P450 (CYP) isoforms CYP3A4 and CYP2C8 in microsomes prepared from HepG2 cells e... | |||
TQ0300 | Conduritol B epoxide | Glucosidase | |
Conduritol B epoxide is an irreversible inhibitor of β-glucosidase (GCase). | |||
T35973 | Cholesterol-5α,6α-epoxide | Epoxycholesterol,5α,6α-epoxy Cholestanol,NSC 18176 | Others |
Cholesterol-5α,6α-epoxide (Epoxycholesterol) is the metabolite of cholesterol produced by oxidation. Cholesterol-5α,6α-epoxide induces triacylglycerol biosynthesis by binding to LXRβ following tamoxifen and PBPE applicat... | |||
T36730 | Vitamin K1 2,3-epoxide | Vitamin K1 epoxide,Phylloquinone oxide,Vitamin K1 2,3-epoxide | Others |
Vitamin K1 2,3-epoxide (Phylloquinone oxide) is reduced to vitamin k and is involved in the vitamin k cycle. | |||
T83857 | Soluble Epoxide Hydrolase PROTAC 1a | sEH Proteolysis-targeting Chimera 1a,Soluble Epoxide Hydrolase Proteolysis-targeting Chimera 1a,sEH PROTAC 1a | |
Soluble epoxide hydrolase (sEH) PROTAC 1a is a proteolysis-targeting chimera (PROTAC) comprising a cereblon ligand linked to the sEH inhibitor t-TUCB via a linker, promoting selective sEH degradation and inhibiting its h... | |||
T29690 | Aflatoxin G1 9,10-epoxide | ||
Aflatoxin G1 9,10-epoxide is a biochemical. | |||
T12974 | Soluble epoxide hydrolase inhibitor | Others | |
Soluble epoxide hydrolase inhibitor is a soluble epoxide hydrolase inhibitor (human soluble epoxide hydrolase (h-sEH) with pIC50 of 8.4). | |||
T32059 | Hepaxanthin | Vitamin A epoxide | |
Hepaxanthin is a carotenoid. | |||
T34627 | SFO | Safrole epoxide,Safrole oxide | |
SFO is an endothelial-to-mesenchymal transition (EndoMT) inducer. | |||
T7898 | AUDA | Epoxide Hydrolase | |
AUDA is an inhibitor of sEH(IC50 values of 18 and 69 nM for the mouse and human enzymes, respectively) | |||
T7199 | TPPU | Epoxide Hydrolase | |
TPPU is a potent inhibitor of both human and mouse sEH (IC50 of 3.7 and 2.8 nM, respectively) | |||
T34070 | Piperitenone oxide | Rotundifolone,Lippione,cis-Piperitenone epoxide,Piperitenone oxide, (+-)- | |
Piperitenone oxide is a major chemical constituent of the carvone pathway MS essential oil. | |||
T14557 | BI-1935 | Epoxide Hydrolase | |
BI-1935 is an inhibitor of soluble epoxide hydrolase (sEH). For diseases related to cardiovascular disease. | |||
T130051 | Detigloylswietenine, 2-Hydroxy, 8?,30?-epoxide, 3- | ||
Detigloylswietenine, 2-Hydroxy, 8?,30?-epoxide, 3- is a useful organic compound for research related to life sciences and the catalog number is T130051. | |||
T10900 | CUDA | PPAR , Epoxide Hydrolase | |
CUDA is an effective soluble cyclohydrolase inhibitor with IC50 of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively. CUDA selectively increases the activity of peroxisome proliferator-activated receptor (PPAR... | |||
T14315 | AR-9281 | APAU | Epoxide Hydrolase |
AR-9281 (APAU) is a potent and selective inhibitor of soluble epoxide hydrolase (s-EH) potentially for the treatment of hypertension and type 2 diabetes | |||
T17158 | Trans-AUCB | t-AUCB | Epoxide Hydrolase |
trans-AUCB (t-AUCB) is an effective and selective soluble epoxide hydrolase inhibitor (IC50s: 1.3 nM, 8 nM, 8 nM for hsEH, mouse sEH and rat sEH, respectively). | |||
T11147 | EC5026 | BPN-19186 | Epoxide Hydrolase |
EC5026 (BPN-19186) has the potential to relieve pain by stabilizing natural analgesic and anti-inflammatory mediators. | |||
T8844 | Diflapolin | Others , FLAP , Epoxide Hydrolase | |
Diflapolin is a highly active dual 5-lipoxygenase-activating protein (FLAP)/soluble epoxide hydrolase (sEH) inhibitor with marked anti-inflammatory efficacy and high target selectivity. | |||
T17196 | UC-1728 | t-TUCB | Epoxide Hydrolase |
UC-1728 (t-TUCB) is an effective rabbit soluble epoxide hydrolase inhibitor (IC50: 2 nM on rabbit liver). | |||
T21859 | ARM1 | Aminopeptidase , Epoxide Hydrolase | |
ARM1 is a potent inhibitor of aminopeptidase and epoxide hydrolase. The IC50 values are 7.61 µM for aminopeptidase and 12.4 µM for epoxide hydrolase. | |||
T15430 | GSK2256294A | GSK 2256294 | Others , Epoxide Hydrolase |
GSK2256294A (GSK 2256294) is potent, selective inhibitor of recombinant human, rat and mouse sEH with IC50 of 27 pM, 61 pM and 189 pM, respectively. | |||
T0355 | Valpromide | Depamide,Valpramide,Dipropylacetamide,2-propylpentanamide | Epoxide Hydrolase , HSV |
Valpromide (Dipropylacetamide) is a carboxamide derivative of valproic acid, used in the treatment of epilepsy and some affective disorders. | |||
T8315 | 1-Cyclohexyl-3-dodecyl urea | CDU,N-Cyclohexyl-N-dodecyl urea,NCND | Epoxide Hydrolase |
1-Cyclohexyl-3-dodecyl urea (NCND) is a highly selective soluble epoxide hydrolase (sEH) inhibitor. | |||
T23044 | N,N'-Dicyclohexylurea | DCU,1,3-Dicyclohexylurea,NSC 17013,Dicyclohexylurea,Dicyclohexylcarbodiamide,AURORA KA-3582 | Epoxide Hydrolase |
N,N'-Dicyclohexylurea (AURORA KA-3582) is a soluble epoxide hydrolase (sEH) inhibitor. | |||
T131605 | Crotepoxide (Futoxide) | ||
Crotepoxide (Futoxide) is a useful organic compound for research related to life sciences and the catalog number is T131605. | |||
T2716 | 1,3-Diphenylurea | Epoxide Hydrolase | |
1, 3-Diphenylurea is involved with Epoxide hydrolase activity. | |||
T17025 | Tecarfarin | ATI-5000,ATI-5923 | Others |
Tecarfarin (ATI-5923) is an orally active and potent vitamin K epoxide reductase (VKOR) antagonist and cannabinoid-1 receptor inverse agonist with antithrombotic activity that attenuates abdominal pain and increases inte... | |||
T60358 | SEH inhibitor-7 | Epoxide Hydrolase | |
sEH inhibitor-7 is a soluble epoxide hydrolase (sEH) inhibitor that inhibits sEH in human and mouse with IC 50 s of 6.2 μM and 0.15 μM, respectively. sEH inhibitor-7 is associated with anti-inflammatory active molecules. | |||
T38367 | CAY10640 | sEH inhibitor-1 | Epoxide Hydrolase |
CAY10640 (sEH inhibitor-1) is a potent, orally active, water-soluble epoxide hydrolase (sEH) inhibitor that inhibits sEH in humans and mice with IC50s of 0.4 and 5.3 nM, respectively. | |||
T9832 | (Rac)-EC5026 | Urea, N-[3-fluoro-4-(trifluoromethoxy)phenyl]-N'-[1-(2-methyl-1-oxobutyl)-4-piperidinyl]- | Epoxide Hydrolase |
(Rac)-EC5026 ((Rac)-BPN-19186) is a potent piperidine inhibitor of soluble epoxide hydrolase (sEH) with Ki of 0.06 nM. (Rac)-EC5026 can be used for the research of Parkinson's disease and dementia with Lewy Bodies (DLB) ... | |||
T63536 | Dual FAAH/sEH-IN-1 | FAAH , Epoxide Hydrolase | |
Dual FAAH/sEH-IN-1 is a dual inhibitor of sEH (soluble epoxide hydrolase) (IC50: 9.6 nM) and FAAH (fatty acid amide hydrolase) (IC50: 7 nM) with high affinity and anti-inflammatory activity. | |||
T36696 | DMBA | ||
7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.1,2It undergoes metabolic activation by numerous enzy... | |||
T68786 | Orniplabin | ||
Orniplabin, also known as SMTP-7 is a dual inhibitor of thrombolysis and soluble epoxide hydrolase. SMTP-7 promotes thrombolysis and inhibits soluble epoxide hydrolase. | |||
T24778 | SEH-IN-12 | sEH inhibitor 12,sEH-inhibitor-12 | |
sEH-IN-12 is an effective inhibitor of the enzyme soluble epoxide hydrolase (sEH). | |||
T32310 | Johnstonol | ||
Johnstonol is an specifically halogenated epoxide obtained from the red alga. | |||
T70626 | MS 347a | ||
MS 347a is a myosin light chain kinase (MLCK) inhibitor; an epoxide analog of sydowinin B (MS-347b). | |||
T32385 | Keto-anhydrokinamycin | ||
Keto-anhydrokinamycin, as a keto-epoxide kinamycin intermediate, is isolated from Streptomyces murayamaensis. | |||
T37334 | (±)11,12-DiHETE | ||
(±)11,12-DiHETE is a dihydroxy metabolite of EPA produced by cytochrome P450-mediated epoxide formation and subsequent hydrolysis by epoxide hydrolase. Plasma levels of (±)11,12-DiHETE are increased over baseline after a... | |||
T17024 | Tecarfarin sodium | ATI-5923 sodium | Others |
Tecarfarin sodium is a novel orally active non-competitive vitamin K epoxide reductase antagonist. Tecarfarin sodium has the antithrombotic activity. | |||
T68259 | TUPS | ||
TUPS is a selective soluble epoxide hydrolase inhibitor which protects against isoprenaline-induced cardiac hypertrophy. | |||
T61541 | SEH inhibitor-6 | ||
sEH inhibitor-6 (Compound 3g) is a highly potent soluble epoxide hydrolase (sEH) inhibitor, exhibiting an IC 50 value of 0.5 nM [1]. | |||
T13042 | SWE101 | Others | |
SWE101 is a potent human and rat soluble epoxide hydrolase (sEH)-P inhibitor(IC50s of 4 μM and 2.8 μM, respectively). | |||
T61690 | MEH-IN-1 | ||
mEH-IN-1 (Compound 62) is a potent inhibitor of microsomal epoxide hydrolase (mEH), with an IC50 value of 2.2 nM. mEH is an α/β-fold hydrolase enzyme that is widely expressed in various mammalian tissues, responsible for... | |||
T37226 | (±)7(8)-EpDTE | ||
(±)7(8)-EpDTE is an oxylipin and an oxidative metabolite of docosapentaenoic acid . It is formed via cytochrome P450 (CYP) metabolism of DPA, and can be further metabolized to (±)7(8)-DiHDTE by epoxide hydrolase. | |||
T37239 | (±)19(20)-EpDTE | ||
(±)19(20)-EpDTE is an oxylipin and an oxidative metabolite of docosapentaenoic acid . It is formed via cytochrome P450 (CYP) metabolism of DPA and can be further metabolized to (±)19(20)-DiHDTE by epoxide hydrolase. | |||
T64136 | SEH inhibitor-5 | ||
sEH inhibitor-5 is a potent inhibitor of sEH (soluble epoxide hydrolase) (IC50: 0.1 nM). | |||
T35493 | (±)10(11)-EpDPA | ||
Cytochrome P450 metabolism of polyunsaturated fatty acids produces numerous bioactive epoxide regioisomers. (±)10(11)-EpDPA is a docosahexaenoic acid epoxygenase metabolite, derived via epoxidation of the 10,11-double bo... | |||
T72698 | SEH inhibitor-14 | ||
sEH inhibitor-14, a benzoxazolone-5-urea analogue, acts as an efficient soluble Epoxide Hydrolase (sEH) inhibitor, demonstrating significant activity with an IC50 value of 0.39 nM. |
カタログ番号 | 製品名 | 別名 | ターゲット |
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TN4958 | Schisandrin C epoxide | Others | |
Schisandrin C epoxide is a natural product for research related to life sciences. The catalog number is TN4958 and the CAS number is 81345-36-0. | |||
TN4130 | Germacrone 4,5-epoxide | gp120/CD4 , IL Receptor , P450 | |
(4S,5S)-(+)-Germacrone-4,5-epoxide inhibits certain subtypes of cytochrome P450 (CYP). | |||
TN4229 | Humulene epoxide II | Antifection | |
Humulene epoxide II has antimalarial activity. | |||
TN6794 | N-(3-methoxybenzyl)-octadecanamide | Others | |
N-(3-methoxybenzyl)-octadecanamide deverts from Maca (Lepidium meyenii Walp.). | |||
TN1078 | Seneciphylline | P450 , GST | |
Seneciphylline, one of the hepatotoxic pyrolizidine alkaloids, has mutagenic activity in Drosophila and their transfer into rat milk.Seneciphylline can significantly increased the activities of epoxide hydrase and glutat... | |||
TN5329 | Epitulipinolide diepoxide | ||
Epitulipinolide diepoxide has antioxidative and chemopreventive activities in skin melanoma cells, can significantly inhibit the proliferation of melanoma cells, it possesses cytotoxic activity against KB cells. | |||
T73797 | Cladospirone bisepoxide | ||
Cladospirone bisepoxide, a metabolite isolated from fungal cultures, exhibits selective antibiotic activity against various bacteria and fungi, and at low concentrations, it inhibits the germination of Lepidium sativum [... | |||
T15039 | Cytochalasin E | Others | |
Cytochalasin E is a potent actin depolymerization agent and an epoxide containing Aspergillus-derived fungal metabolite. Cytochalasin E also inhibits angiogenesis and tumor growth. It binds and caps the barbed end of act... | |||
T37272 | 9(S),12(S),13(S)-TriHOME | ||
9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble ... | |||
TN4592 | Murrangatin | IL Receptor , TNF , COX , Prostaglandin Receptor | |
Murrangatin may be a valuable anti-tumor-promoting agent, it can significantly inhibit Epstein-Barr virus early antigen (EBV-EA) activation, and preserve the high viability of Raji cells, it also exhibits cytotoxicity ag... |
カタログ番号 | 製品名 | Species | Expression System |
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TMPY-00410 | EPHX2 Protein, Human, Recombinant (His) | Human | Baculovirus Insect Cells |
Genetic variation in EPHX2 was significantly associated with risk of incident CHD in Caucasians, implicating EPHX2 as a potential cardiovascular disease-susceptibility gene. Single nucleotide polymorphisms (SNPs) in the ... | |||
TMPH-01298 | EPHX1 Protein, Human, Recombinant (His) | Human | E. coli |
Biotransformation enzyme that catalyzes the hydrolysis of arene and aliphatic epoxides to less reactive and more water soluble dihydrodiols by the trans addition of water. Plays a role in the metabolism of endogenous lip... | |||
TMPJ-01326 | HDHD2 Protein, Human, Recombinant (His) | Human | E. coli |
Haloacid Dehalogenase-Like Hydrolase Domain-Containing Protein 22 (HDHD2) is a member of the HAD-like hydrolase superfamily. HDHD2 includes L-2-Haloacid Dehalogenase, Epoxide Hydrolases and Phosphatases. There are two ac... |