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Vindesine (sulfate) (Standard)

CAT: 0804-HY-129071RSize: 1 EachDry Ice: NoHazardous: No
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Description
Vindesine (sulfate) (Standard) is the analytical standard of Vindesine (sulfate) . This product is intended for research and analytical applications. Vindesine sulfate is a potent tubulin inhibitor with an Ki of 0.110 μM. Vindesine sulfate shows anti-proliferation effect in vitro. Vindesine sulfate shows antitumor effect in vivo[1].
CAS Number
59917-39-4
UNSPSC
12352005
Target
Microtubule/Tubulin; Reference Standards
Type
Reference Standards
Related Pathways
Cell Cycle/DNA Damage; Cytoskeleton; Others
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/vindesine-sulfate-standard.html
Smiles
O=S(O)(O)=O.CC[C@@]12[C@@]3([H])[C@@]4(CCN3CC=C2)C5=CC([C@@]6(C7=C(CC[N@]8C[C@@](C[C@](O)(C8)CC)([H])C6)C9=CC=CC=C9N7)C(OC)=O)=C(OC)C=C5N([C@@]4([H])[C@](O)([C@@H]1O)C(N)=O)C
Molecular Formula
C43H57N5O11S
Molecular Weight
852.00
References & Citations
[1]Jordan MA, et al. Comparison of the effects of vinblastine, vincristine, vindesine, and vinepidine on microtubule dynamics and cell proliferation in vitro. Cancer Res. 1985 Jun;45 (6) :2741-7.
Shipping Conditions
Room temperature
Scientific Category
Reference Standards

Chemical Information

Vindesine Sulfate

Vindesine sulfate is an alkaloid sulfate salt. It has a role as an antineoplastic agent. It is functionally related to a vindesine.

CAS Number59917-39-4
PubChem CID43116
IUPAC Namemethyl (13S,15S,17S)-13-[(1R,9R,10S,11R,12R,19R)-10-carbamoyl-12-ethyl-10,11-dihydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl]-17-ethyl-17-hydroxy-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraene-13-carboxylate;sulfuric acid
Molecular FormulaC43H57N5O11S
Molecular Weight852.0
Topological Polar Surface Area248
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count14
Rotatable Bond Count7
Heavy Atom Count60
Formal Charge0
Complexity1650
SMILES
CC[C@@]1(C[C@@H]2C[C@@](C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)[C@]78CCN9[C@H]7[C@@](C=CC9)([C@H]([C@@]([C@@H]8N6C)(C(=O)N)O)O)CC)OC)C(=O)OC)O.OS(=O)(=O)O
InChI
InChI=1S/C43H55N5O7.H2O4S/c1-6-39(52)21-25-22-42(38(51)55-5,33-27(13-17-47(23-25)24-39)26-11-8-9-12-30(26)45-33)29-19-28-31(20-32(29)54-4)46(3)35-41(28)15-18-48-16-10-14-40(7-2,34(41)48)36(49)43(35,53)37(44)50;1-5(2,3)4/h8-12,14,19-20,25,34-36,45,49,52-53H,6-7,13,15-18,21-24H2,1-5H3,(H2,44,50);(H2,1,2,3,4)/t25-,34+,35-,36-,39+,40-,41-,42+,43+;/m1./s1
InChIKey
COFJBSXICYYSKG-FJFFLIEUSA-N
Chemical Structure
2D Structure
2D structure of Vindesine Sulfate
CAS: 59917-39-4
CID: 43116
Formula: C43H57N5O11S
MW: 852.0
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight852.0
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count14
Rotatable Bond Count7
Exact Mass851.37752882
Monoisotopic Mass851.37752882
Topological Polar Surface Area248 Ų
Heavy Atom Count60
Formal Charge0
Complexity1650
Isotope Atom Count0
Defined Atom Stereocenter Count9
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes

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Alternative Products

CatalogName
MBS3614220-01Vindesine sulfate
291927-01Vindesine sulfate salt
RM-V091401-01Vindesine Sulfate EP Impurity A
BV164524Vindesine sulfate - Bio-X TM
RM-V091403-01Vindesine Sulfate EP Impurity C
MBS6107671-01Vindesine Sulfate Salt (LY-099094, Eldisine, Fildesin)
RM-V091402-01Vindesine Sulfate EP Impurity B; Vincristine EP Impurity H
ASSO492YSulfate Standard for Ion Chromatography
TN2299Vindesine

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