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164235414 molecular structure
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sulfuric acid methyl (1R,9R,10S,11R,12R,19R)-11-[(2H3)acetyloxy]-12-ethyl-4-[(13S,15S,17S)-17-ethyl-17-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl]-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate

ChemBase ID: 179504
Molecular Formular: C46H60N4O13S
Molecular Mass: 909.0526
Monoisotopic Mass: 908.387759
SMILES and InChIs

SMILES:
c12c([nH]c3c1CCN1C[C@@H](C[C@]3(C(=O)OC)c3c(cc4c(c3)[C@@]35[C@@H](N4C)[C@]([C@@H]([C@]4([C@@H]3N(CC=C4)CC5)CC)OC(=O)C)(C(=O)OC)O)OC)C[C@](C1)(CC)O)cccc2.S(=O)(=O)(O)O
Canonical SMILES:
OS(=O)(=O)O.COc1cc2N(C)[C@@H]3[C@@]4(c2cc1[C@]1(C[C@@H]2CN(CCc5c1[nH]c1c5cccc1)C[C@](C2)(O)CC)C(=O)OC)CCN1[C@H]4[C@@]([C@H]([C@]3(O)C(=O)OC)OC(=O)C)(CC)C=CC1
InChI:
InChI=1S/C46H58N4O9.H2O4S/c1-8-42(54)23-28-24-45(40(52)57-6,36-30(15-19-49(25-28)26-42)29-13-10-11-14-33(29)47-36)32-21-31-34(22-35(32)56-5)48(4)38-44(31)17-20-50-18-12-16-43(9-2,37(44)50)39(59-27(3)51)46(38,55)41(53)58-7;1-5(2,3)4/h10-14,16,21-22,28,37-39,47,54-55H,8-9,15,17-20,23-26H2,1-7H3;(H2,1,2,3,4)/t28-,37+,38-,39-,42+,43-,44-,45+,46+;/m1./s1
InChIKey:
KDQAABAKXDWYSZ-JKDPCDLQSA-N

Cite this record

CBID:179504 http://www.chembase.cn/molecule-179504.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
sulfuric acid methyl (1R,9R,10S,11R,12R,19R)-11-[(2H3)acetyloxy]-12-ethyl-4-[(13S,15S,17S)-17-ethyl-17-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl]-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate
IUPAC Traditional name
sulfuric acid methyl (1R,9R,10S,11R,12R,19R)-11-[(2H3)acetyloxy]-12-ethyl-4-[(1S,13S,15S,17S)-17-ethyl-17-hydroxy-13-(methoxycarbonyl)-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl]-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate
Synonyms
Vincaleukoblastine-d3 Sulfate
(+)-Vinblastine-d3 Sulfate
Rozevin-d3
VLB-d3
Valban-d3
Vinblastin-d3
29060-LE-d3
Exal-d3
Velban-d3
Velbe-d3
Vinblastine-d3 Sulfate
PubChem SID
164235414
PubChem CID
71752947

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC V314002 external link Add to cart
PubChem 71752947 external link
Data Source Data ID Price
TRC
V314002 external link Add to cart Please log in.
Data Source Data ID
PubChem 71752947 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 10.869524  H Acceptors
H Donor LogD (pH = 5.5) -1.6706752 
LogD (pH = 7.4) 1.8057727  Log P 4.1831455 
Molar Refractivity 222.4206 cm3 Polarizability 87.76486 Å3
Polar Surface Area 154.1 Å2 Rotatable Bonds 10 
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
MSDS Link
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Certificate of Analysis
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DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - V314002 external link
Labelled Vinblastine (V314000). Antitumor alkaloid isolated from periwinkle, Vinca rosea Linn., Apocynaceae; inhibits microtubule assembly. An antineoplastic.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Lu, C., et al.: Cancer Research, 39, 3575 (1979)
  • • Gobbi, P.G., et al.: J. Clin. Oncol., 14, 527 (1979)
  • • Muhtadi, F.J., et al.: Anal. Profiles Drug Subs. Excip., 21, 611 (1979)
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PATENTS

PATENTS

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INTERNET

INTERNET

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