Home > Compound List > Compound details
164235415 molecular structure
click picture or here to close

methyl (1R,9R,10S,11S,12R,19R)-11-(acetyloxy)-12-ethyl-4-[(13S,15S,17S)-17-ethyl-17-hydroxy-13-[(2H3)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: 179505
Molecular Formular: C46H58N4O9
Molecular Mass: 810.97412
Monoisotopic Mass: 810.42037946
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
Canonical SMILES:
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/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/h10-14,16,21-22,28,37-39,47,54-55H,8-9,15,17-20,23-26H2,1-7H3/t28-,37+,38-,39+,42+,43-,44-,45+,46+/m1/s1
InChIKey:
JXLYSJRDGCGARV-SSFPKTLXSA-N

Cite this record

CBID:179505 http://www.chembase.cn/molecule-179505.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
methyl (1R,9R,10S,11S,12R,19R)-11-(acetyloxy)-12-ethyl-4-[(13S,15S,17S)-17-ethyl-17-hydroxy-13-[(2H3)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
methyl (1R,9R,10S,11S,12R,19R)-11-(acetyloxy)-12-ethyl-4-[(1S,13S,15S,17S)-17-ethyl-17-hydroxy-13-[(2H3)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
29060-LE-d3
Exal-d3
Velban-d3
Velbe-d3
Vinblastine-d3
Vincaleukoblastine-d3 Sulfate
(+)-Vinblastine-d3 Sulfate
Rozevin-d3
VLB-d3
Valban-d3
Vinblastin-d3
PubChem SID
164235415
PubChem CID
71752949

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC V314003 external link Add to cart
PubChem 71752949 external link
Data Source Data ID Price
TRC
V314003 external link Add to cart Please log in.
Data Source Data ID
PubChem 71752949 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

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Chloroform expand Show data source
Dichloromethane expand Show data source
Dimethyl Sulfoxide expand Show data source
Methanol expand Show data source
Apperance
Beige Solid expand Show data source
Storage Condition
Refrigerator expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
Download expand Show data source

DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - V314003 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)
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle