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Cyclopropyl(2,6-difluorophenyl)methanone
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Cyclopropyl(2,6-difluorophenyl)methanone
Catalog Number:
(101780-932)
Catalog Number:
(76082-164)
Supplier:
Bioss
Description:
This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5(S)-trans-7,9-trans-11,14-cis-eicosatetrenoic acid (leukotriene A4). Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined.
Catalog Number:
(75835-544)
Supplier:
Restek
Description:
The mix consists of acetonitrile, acrylonitrile, allyl chloride , benzene, bromobenzene, bromochloromethane, bromodichloromethane, bromoform, n-butylbenzene, sec-butylbenzene, tert-butylbenzene, carbon disulfide, carbon tetrachloride, chlorobenzene, 2-chloroethanol, chloroform, chloroprene , 2-chlorotoluene, 4-chlorotoluene, dibromochloromethane, 1,2-dibromo-3-chloropropane , 1,2-dibromoethane , dibromomethane, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene, cis-1,4-dichloro-2-butene, trans-1,4-dichloro-2-butene, 1,1-dichloroethane, 1,2-dichloroethane, 1,1-dichloroethene, cis-1,2-dichloroethene, trans-1,2-dichloroethene, 1,2-dichloropropane, 1,3-dichloropropane, 2,2-dichloropropane, 1,1-dichloropropene, cis-1,3-dichloropropene, trans-1,3-dichloropropene, diethyl ether , 1,4-dioxane, ethylbenzene, ethyl methacrylate, hexachloro-1,3-butadiene, iodomethane , isobutyl alcohol , isopropylbenzene , 4-isopropyl toluene , methacrylonitrile, methyl acrylate, methyl methacrylate, methylene chloride , naphthalene, nitrobenzene, 2-nitropropane, propionitrile, n-propylbenzene, styrene, 1,1,1,2-tetrachloroethane, 1,1,2,2-tetrachloroethane, tetrachloroethene, tetrahydrofuran, toluene, 1,2,3-trichlorobenzene, 1,1,1-trichloroethane, 1,1,2-trichloroethane, trichloroethene, 1,2,3-trichloropropane, 1,1,2-trichlorotrifluororethane , 1,2,4-trimethylbenzene, 1,3,5-trimethylbenzene, m-xylene, o-xylene, p-xylene.
Catalog Number:
(10104-052)
Supplier:
Prosci
Description:
RDH12 is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. RDH12 also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).
Catalog Number:
(76082-166)
Supplier:
Bioss
Description:
This gene encodes a member of the lipoxygenase gene family and plays a dual role in the synthesis of leukotrienes from arachidonic acid. The encoded protein, which is expressed specifically in bone marrow-derived cells, catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8,11,14-cis-eicosatetraenoic acid, and further to the allylic epoxide 5(S)-trans-7,9-trans-11,14-cis-eicosatetrenoic acid (leukotriene A4). Leukotrienes are important mediators of a number of inflammatory and allergic conditions. Mutations in the promoter region of this gene lead to a diminished response to antileukotriene drugs used in the treatment of asthma and may also be associated with atherosclerosis and several cancers. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined.
Catalog Number:
(TCA1698-100MG)
Supplier:
TCI America
Description:
CAS Number: 21293-29-8
Molecular Formula: C15H20O4
Molecular Weight: 264.32
Purity/Analysis Method: <gt/>98.0% (HPLC)
Form: Crystal
Melting point (°C): 163
Specific rotation [a]20/D: 410 deg (C=0.2, EtOH)
Storage Temperature: 0-10°C
Supplier:
Bachem Americas
Description:
A readily soluble, specific and sensitive substrate for chymotrypsin and human pancreatic elastase. It is also hydrolyzed by cathepsin G and chymase. Furthermore it is the standard substrate for FK-506 binding proteins (FKBPs, also called macrophilins) and cyclophilins, which belong to the group of peptidyl prolyl cis-trans isomerases (PPIases). Thus, Suc-AAPF-pNA has been used for an uncoupled protease-free assay of PPIase activity.
Catalog Number:
(10480-606)
Supplier:
Bioss
Description:
Reduces all-trans-retinal and 9-cis retinal. Can also catalyze the oxidation of all-trans-retinol with NADP as co-factor, but with much lower efficiency. Reduces alkyl phenyl ketones and alpha-dicarbonyl compounds with aromatic rings, such as pyrimidine-4-aldehyde, 3-benzoylpyridine, 4-benzoylpyridine, menadione and 4-hexanoylpyridine. Has no activity towards aliphatic aldehydes and ketones.Tissue specificity:Isoform 1 is predominantly expressed in normal cervix (at protein level). Isoform 4 is expressed in some neoplastic cervical tissues, but not in normal cervix (at protein level). Isoform 5 and isoform 6 are expressed in a few neoplastic cervical tissues.
Catalog Number:
(10426-398)
Supplier:
Bioss
Description:
PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.
Catalog Number:
(10426-328)
Supplier:
Bioss
Description:
PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.
Supplier:
Bachem Americas
Description:
Suc-ALPF-pNA, substrate for FK-506 binding proteins (FKBPs, also called macrophilins) and cyclophilins, which belong to the group of peptidyl prolyl cis-trans isomerases (PPIases). This tetrapeptide has been used for an uncoupled protease-free assay of PPIase activity.
Catalog Number:
(TS34240-5000)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
(S)-(+)-Abscisic acid ≥98%
Catalog Number:
(10426-394)
Supplier:
Bioss
Description:
PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.
Supplier:
Thermo Scientific Chemicals
Description:
. Grade:tech. 90, Melting Point C. Boiling Point C:130*/6mm. C12H20O. 21662-16-8. KEEP COLD
Catalog Number:
(10426-396)
Supplier:
Bioss
Description:
PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
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