Fenretinide D4

Product Name Fenretinide D4
Alternate Names Retinoic Acid Stable Isotopes, Stable Isotopes of Retinoic Acid
CAT No. CS-O-06618
CAS No. 65646-68-6(Unlabeled)
Category Stable Isotopes
Stock IN-Stock
Mol. Wt. 395.57 g/mol
Mol. For. C26H29D4NO2
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Retinoic Acid
Purity 98.74
Smileys CC(/C=C/C(C(C)(CCC1)C)=C1C)=C\C=C\C(C)=C\C(NC2=C([2H])C([2H])=C(O)C([2H])=C2[2H])=O
Canonical Smiles CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC(=O)NC2=CC=C(C=C2)O)C)C
InchIKey AKJHMTWEGVYYSE-FXILSDISSA-N
Inchl InChI=1S/C26H33NO2/c1-19(11-16-24-21(3)10-7-17-26(24,4)5)8-6-9-20(2)18-25(29)27-22-12-14-23(28)15-13-22/h6,8-9,11-16,18,28H,7,10,17H2,1-5H3,(H,27,29)/b9-6+,16-11+,19-8+,20-18+
IUPAC (2E,4E,6E,8E)-N-(4-hydroxyphenyl)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenamide
Controlled No
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Fenretinide D4 is a synthetic retinoid, which is a derivative of vitamin A. It is used in the treatment of cancer and other diseases. The drug is known to induce apoptosis, or programmed cell death, in cancer cells, which makes it a promising option for cancer therapy. Fenretinide D4 works by binding to retinoic acid receptors (RARs), which are proteins found in the nucleus of cells. This binding activates a series of signaling pathways that ultimately lead to the induction of apoptosis in cancer cells. Fenretinide D4 has also been shown to have anti-inflammatory and anti-angiogenic properties, which means it can inhibit the growth of new blood vessels that tumors need to survive. In terms of chemical information, Fenretinide D4 is a stable isotopic labeled form of fenretinide, which means it is a modified version of the original drug. The molecular formula of Fenretinide D4 is C26H35D4NO2, and its chemical name is 4-oxo-N-(4-hydroxyphenyl)retinamide-d4. Overall, Fenretinide D4 is a promising drug for the treatment of cancer and other diseases. Its ability to induce apoptosis in cancer cells and inhibit the growth of new blood vessels make it a valuable option for cancer therapy.

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