4-Aminocyclohexanecarboxylic+acid+(mixture+of+cis+and+trans+isome
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Supplier:
AMBEED, INC
Description:
Zeatin riboside 96%
Catalog Number:
(76480-790)
Supplier:
AAT BIOQUEST INC
Description:
In general, rhodamine 6G conjugates have higher fluorescence quantum yields than tetramethylrhodamine conjugates, as well as good photostability.
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Supplier:
BeanTown Chemical
Description:
CAS: 92112-69-1; EC No: 295-570-2; MDL No: MFCD02179311
UN No: UN1208; Haz Class: 3; Packing Group: II
Liquid; Molecular Formula: C6H14; MW: 86.18
Melting Point: -95°; Boiling Point: 68-70°; Flash point: -23°C (-9°F)
Density (g/mL): 0.672; Refractive Index: 1.379
Supplier:
Bachem Americas
Description:
Sequence: H-His(Bzl)-OMe · 2 HCl
Catalog Number:
(IC15211905)
Supplier:
MP Biomedicals
Description:
Tetramisole is an alkaline phosphatase inhibitor. It is a racemic mixture of (+) and (-) isomers. The (-) isomer (levamisole) accounts for most of the biological activity of tetramisole.
Catalog Number:
(76012-302)
Supplier:
Prosci
Description:
The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. Members of this family exhibit PPIase activity and function as molecular chaperones. A similar protein in mouse is located in the endoplasmic reticulum and binds calcium.
Catalog Number:
(101189-698)
Supplier:
BioVendor
Description:
Cyclophilins belong to a group of proteins that have peptidyl-prolyl cis-trans isomerase activity; such proteins are collectively known as immunophilins and also include the FK-506-binding proteins and the parvulins. Cyclophilins are found in all cells of all organisms studied, in both prokaryotes and eukaryotes. Human have a total of 16 cyclophilin proteins. Cyclophilins also have varying degrees of affinity for the immunosuppressive drug Cyclosporine A (CsA), a cyclic 11-amino-acid peptide produced by fungus Tolypocladium infantum. Cyclophilin A, in particular, is the major intracellular receptor for CsA. Cyclophilin A (CYPA) is the first member of the cyclophilins to be identified in mammals. Human genes of CYPA, also known as Cyp18, are located on chromosome 7p11.2-p13 and encode the protein, which consists of 165 amino acid residues with a relative molecular mass approximately 18 kDa. Human CYPA has an eight-stranded antiparallel β-barrel structure, with two α-helices enclosing the barrel from either side. Seven aromatic and other hydrophobic residues form a compact hydrophobic core within the barrel, usually in the area where CsA binds. A loop from Lys118 ti His126 and four β-strands (β3-β6) make up the binding site for CsA. In mammals, the CsA-CYPA complex binds to and inhibits calcineurin, a calcium-calmodulin-activated serine/threonine-specific protein phosphatase. The inhibition of calcineurin blocks the translocation of nuclear factor of activated T cells from the cytosol to the nucleus, thus preventing the transcription of genes encoding cytokines such as interleukin-2.
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Cinnamyl alcohol ≥98% (trans-isomers)
Catalog Number:
(89149-298)
Supplier:
Enzo Life Sciences
Description:
R,S-Sulforaphane is a synthetic version of the naturally occurring compound, R-sulforaphane, from Broccoli. It is a racemic mixture of both the R and S isomers.
Potent, selective inducer of phase II detoxification enzymes. Inhibits chemically induced mammary tumor formation in rats. Inhibits LPS-induced HMGB1 (high mobility group box 1) secretion.
Supplier:
AMBEED, INC
Description:
1-(2-Chlorophenyl)-2-nitroethylene, Purity: 98% (only trans-), CAS Number: 3156-34-1, Appearance: White to Yellow to Tan Powder or Crystals, Storage: Inert atmosphere, Room Temperature, Size: 25g
Supplier:
Thermo Scientific Chemicals
Description:
Trifluoromethyl(perfluorodecahydronaphthalene). Grade:tech. 85, Melting Point C-70*. Boiling Point C:159-160*. C11F20. 51294-16-7. Balance other fluorocarbons.
Supplier:
Bachem Americas
Description:
Sequence: Boc-His(Bzl)-OH
Supplier:
MP Biomedicals
Description:
Protein kinase C inhibitor (IC50 = 50-200 µM depending on assay conditions in MCF-7 cells or IC50 = 100 µM in rat brain). The PKC inhibition is also dependent on the phosopholipid concentration. Also inhibits both calmodulin-dependent and calmodulin-independent Ca2+-, Mg2+-ATPase. Tamoxifen is a selective estrogen response modifier (SERM), anti-angiogenetic factor. It is a prodrug that is metabolized to active metabolites 4-hydroxytamoxifen (4-OHT) and endoxifen by cytochrome P450 isoforms CYP2D6 and CYP3A4. In breast cancer, the gene repressor activity of tamoxifen against ERBB2 is dependent upon PAX2. Blocks estradiol-stimulated VEGF production in breast tumor cells.
Tamoxifen has been used to facilitate the recombination of ect2flox allele in mouse organs. It has also been used to study its effect on lipopolysaccharide (LPS)-induced microglial activation Tamoxifen is a Protein kinase C inhibitor. It induces apoptosis in human malignant glioma cell lines. Tamoxifen and its metabolite 4-hydroxytamoxifen are selective estrogen response modifiers (SERMs) that act as estrogen antagonists in mammary gland. Blocks estradiol-stimulated VEGF production in breast tumor cells.
Supplier:
TCI America
Description:
CAS Number: 122-20-3
MDL Number: MFCD00004533 Molecular Formula: C9H21NO3 Molecular Weight: 191.27 Purity/Analysis Method: >98.0% (T) Form: Crystal Boiling point (°C): 305 Flash Point (°C): 160
Supplier:
Thermo Scientific Chemicals
Description:
Main effects in tissue culture systems include control of shoot growth and formation, cell division and inhibition of leaf senescence
Supplier:
TCI America
Description:
MDL Number: MFCD00008236
Molecular Formula: C5H13N Molecular Weight: 87.17 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Flash Point (°C): -1 Specific Gravity (20/20): 0.76
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