6-a-Hydroxy Paclitaxel-D5

Product Name 6-a-Hydroxy Paclitaxel-D5
Alternate Names Paclitaxel Stable Isotopes, Stable Isotopes of Paclitaxel
CAT No. CS-AU-00064
CAS No. 1315376-90-9
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Paclitaxel
Therapeutic Anti-Cancer / Oncology
Smileys CC(O[C@@]1([C@]([C@@H](O)[C@@H]2O)([H])OC1)[C@@]([C@@]2(C3=O)C)([H])[C@@H]([C@@](C4(C)C)(C[C@H](OC([C@H](O)[C@H](C5=CC=CC=C5)NC(C(C([2H])=C6[2H])=C(C([2H])=C6[2H])[2H])=O)=O)C(C)=C4[C@H]3OC(C)=O)O)OC(C7=CC=CC=C7)=O)=O
Canonical Smiles CC1=C2C(C(=O)C3(C(C(C(C2(C)C)(CC1OC(=O)C(C(C4=CC=CC=C4)NC(=O)C5=CC=CC=C5)O)O)OC(=O)C6=CC=CC=C6)C7(COC7C(C3O)O)OC(=O)C)C)OC(=O)C
InchIKey NDCWHEDPSFRTDA-NZSUPHSRSA-N
Inchl InChI=1S/C47H51NO15/c1-24-30(61-43(57)33(51)32(27-16-10-7-11-17-27)48-41(55)28-18-12-8-13-19-28)22-47(58)40(62-42(56)29-20-14-9-15-21-29)36-45(6,38(54)35(60-25(2)49)31(24)44(47,4)5)37(53)34(52)39-46(36,23-59-39)63-26(3)50/h7-21,30,32-37,39-40,51-53,58H,22-23H2,1-6H3,(H,48,55)/t30-,32-,33+,34-,35+,36-,37-,39+,40-,45-,46+,47+/m0/s1/i8D,12D,13D,18D,19D
IUPAC [(1S,2S,3R,4S,7R,8S,9R,10S,12R,15S)-4,12-diacetyloxy-1,8,9-trihydroxy-15-[(2R,3S)-2-hydroxy-3-[(2,3,4,5,6-pentadeuteriobenzoyl)amino]-3-phenylpropanoyl]oxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate
Controlled No
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6-a-Hydroxy Paclitaxel-D5 is a derivative of Paclitaxel, a natural product extracted from the bark of the Pacific Yew tree. Paclitaxel has been used as an effective chemotherapy agent for various types of cancers such as ovarian, breast, and lung cancer. 6-a-Hydroxy Paclitaxel-D5 is a deuterated analogue of Paclitaxel, where five deuterium atoms are incorporated into the molecule. This modification is done to improve the pharmacokinetic properties of the drug, including increased metabolic stability and decreased toxicity. The primary mechanism of action of Paclitaxel and its derivatives is the inhibition of microtubule depolymerization, leading to cell cycle arrest and apoptosis. 6-a-Hydroxy Paclitaxel-D5 acts in a similar manner and has been shown to have potent antitumor activity in vitro and in vivo. The chemical structure of 6-a-Hydroxy Paclitaxel-D5 includes a hydroxyl group attached to the sixth carbon atom of the Paclitaxel molecule. This modification can affect the drug's solubility, stability, and bioavailability. Therefore, proper storage and handling of the drug are essential to maintain its efficacy. In conclusion, 6-a-Hydroxy Paclitaxel-D5 is a promising chemotherapy agent that has shown significant antitumor activity in preclinical studies. Its chemical modifications have improved its pharmacokinetic properties, making it a potential candidate for clinical trials.

Related Compounds

Paclitaxel-D5 (Benzoylamine) | Paclitaxel-D5 (Benzoyloxy) |

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