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CAS 76429-85-1: 10-Deacetylcephalomannine

Formula:C43H51NO13
InChI:InChI=1S/C43H51NO13/c1-8-22(2)37(50)44-31(25-15-11-9-12-16-25)33(48)39(52)55-27-20-43(53)36(56-38(51)26-17-13-10-14-18-26)34-41(7,35(49)32(47)30(23(27)3)40(43,5)6)28(46)19-29-42(34,21-54-29)57-24(4)45/h8-18,27-29,31-34,36,46-48,53H,19-21H2,1-7H3,(H,44,50)/b22-8+/t27-,28-,29+,31-,32+,33+,34-,36-,41+,42-,43+/m0/s1
InChI key:InChIKey=ADDGUHVEJPNWQZ-GJKIWTKTSA-N
SMILES:O(C(C)=O)[C@]12[C@]3([C@H](OC(=O)C4=CC=CC=C4)[C@@]5(O)C(C)(C)C([C@@H](O)C(=O)[C@]3(C)[C@@H](O)C[C@]1(OC2)[H])=C(C)[C@@H](OC([C@@H]([C@@H](NC(/C(=C/C)/C)=O)C6=CC=CC=C6)O)=O)C5)[H]
Synonyms:
  • 10-Deacetylcephalomannine
  • 10-Deacetyltaxol B
  • 10β-Deacetylcephalomanine
  • 7,11-Methano-1H-cyclodeca[3,4]benz[1,2-b]oxete, benzenepropanoic acid deriv.
  • Benzenepropanoic acid, α-hydroxy-β-[(2-methyl-1-oxo-2-butenyl)amino]-, 12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,6,11-trihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, [2aR-[2aα,4β,4aβ,6β,9α[αR*,βS*(E)],11α,12α,12aα,12bα]]-
  • Benzenepropanoic acid, α-hydroxy-β-[[(2E)-2-methyl-1-oxo-2-buten-1-yl]amino]-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,6,11-trihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, (αR,βS)-
  • Benzenepropanoic acid, α-hydroxy-β-[[(2E)-2-methyl-1-oxo-2-butenyl]amino]-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,6,11-trihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, (αR,βS)-
  • benzenepropanoic acid, alpha-hydroxy-beta-[[(2E)-2-methyl-1-oxo-2-buten-1-yl]amino]-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,6,11-trihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl ester, (alphaR,betaS)-
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Found 6 products.
  • 10-Deacetyl Cephalomannine

    CAS:
    Applications 10-Deacetyl Cephalomannine is a derivative of Cephalomannine (C258500). References Liu, J., et al.: J. Pharm. Biomed. Anal., 15, 1729 (1997), Montero, A., et al.: Lancet Oncol., 6, 229 (2005), Ojima, I., et al.: J. Nat. Prod. 72, 554 (2009),
    Formula:C43H51NO13
    Color and Shape:Neat
    Molecular weight:789.86

    Ref: TR-D198650

    25mg
    765.00€
    50mg
    1,425.00€
    100mg
    2,256.00€
  • 10-Deacetyl Cephalomannine

    CAS:
    Formula:C43H51NO3
    Molecular weight:789.87

    Ref: ST-EA-CP-C548001

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  • 10-Deacetyl Cephalomannine

    CAS:
    Formula:C43H51NO3
    Molecular weight:789.88

    Ref: 4Z-C-11905

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  • 10-Deacetyl cephalomannine

    CAS:
    10-Deacetyl cephalomannine is a taxane derivative that has been isolated from the needles of Taxus cuspidata. This compound is metabolized by human liver enzymes, such as cytochrome P450, to 10-deacetyltaxol (10-DT). 10-DT has shown antitumor activity in vitro and in vivo against human cancer cell lines. It also inhibits the growth of Mycobacterium tuberculosis in culture. The mechanism of action for this compound is not known, but it may inhibit protein synthesis or cell division. 10-DT inhibits the growth of cancer cells by binding to tubulin and inhibiting microtubule polymerization.
    Formula:C43H51NO13
    Purity:Min. 95%
    Molecular weight:789.86 g/mol

    Ref: 3D-FD20817

    10mg
    749.00€
    25mg
    989.00€
  • N-Tigloyl Docetaxel

    CAS:
    Formula:C43H51NO13
    Molecular weight:789.9

    Ref: ST-EA-CP-D32046

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  • 10-Deacetylcephalomannine

    CAS:
    10-Deacetylcephalomannin exhibits activity against PS leukemia in vivo; however, its instability leads to an equilibrium mixture with its cytotoxic C-7 epimer. Additionally, 10-Deacetylcephalomannine demonstrates growth inhibitory effects on human cancer cell lines, including cervical HeLa adenocarcinoma.
    Formula:C43H51NO13
    Color and Shape:Solid
    Molecular weight:789.9

    Ref: TM-TN7414

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