cis-\u200BEthyl+4-\u200Baminocyclohexanecarb\u200Boxylate+HCl+sal
Your search request has been modified to limit number of results. Your search was - cis-\u200BEthyl+4-\u200Baminocyclohexanecarb\u200Boxylate+HCl+salt |
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Supplier:
Enzo Life Sciences
Description:
Cyclic hydroxylamine spin probe for<i> in vivo</i>, intraperitoneal and intravenous injections.
Catalog Number:
(77402-368)
Supplier:
APOLLO SCIENTIFIC
Description:
2-Chloroethylammonium chloride 97%
Supplier:
VWR International
Description:
General purpose nuclear stain, regressive type. Used with hematoxylin and eosin staining.
Supplier:
AMBEED, INC
Description:
Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one, 2',4',5',7'-tetrabromo-3',6'-dihydroxy-, Purity: 97% BS, CAS Number: 15086-94-9, Appearance: Reddish yellow to red powder or crystals, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 100g
Supplier:
AMBEED, INC
Description:
Ethyl azetidine-3-carboxylate hydrochloride, Purity: 97%, CAS Number: 405090-31-5, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 10G
Supplier:
Thermo Scientific Chemicals
Description:
D-Tyrosine methyl ester hydrochloride, 98%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Mexiletine hydrochloride
Supplier:
Matrix Scientific
Description:
MF=C7H8Clf3N2 MW=212.60 Cas=3107-34-4 MDL=MFCD00102619 ,25G
Supplier:
AMBEED, INC
Description:
Pyren-1-ylmethanamine hydrochloride, Purity: 97%, CAS Number: 93324-65-3, Appearance: Powder or crystals, Storage: Sealed in dry, Room Temperature, Size: 250mg
Supplier:
TCI America
Description:
3-Fluoroazetidine Hydrochloride, Purity: >98.0%(N)(T), CAS Number: 617718-46-4, Molecular Formula: C3H6FN.HCl, Molecular Weight: 111.54, form: Crystal- Powder, Color: White - Almost white, Size: 1G
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:
MP Biomedicals
Description:
Soluble in methanol (50 mg/mL - clear, colorless solution). Soluble in water (50 mg/mL).
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-(2-Aminoethyl)-2-methoxyphenol hydrochloride 99+%
Supplier:
AMBEED, INC
Description:
H-D-Dap(Boc)-OMe 97%
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