Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C46H56N4O10 |
Molecular Weight | 824.9576 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 9 / 9 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12N3CC[C@@]14C5=CC(=C(OC)C=C5N(C=O)[C@@]4([H])[C@](O)([C@H](OC(C)=O)[C@]2(CC)C=CC3)C(=O)OC)[C@]6(C[C@H]7CN(C[C@](O)(CC)C7)CCC8=C6NC9=CC=CC=C89)C(=O)OC
InChI
InChIKey=OGWKCGZFUXNPDA-CFWMRBGOSA-N
InChI=1S/C46H56N4O10/c1-7-42(55)22-28-23-45(40(53)58-5,36-30(14-18-48(24-28)25-42)29-12-9-10-13-33(29)47-36)32-20-31-34(21-35(32)57-4)50(26-51)38-44(31)16-19-49-17-11-15-43(8-2,37(44)49)39(60-27(3)52)46(38,56)41(54)59-6/h9-13,15,20-21,26,28,37-39,47,55-56H,7-8,14,16-19,22-25H2,1-6H3/t28-,37-,38+,39+,42-,43+,44+,45-,46-/m0/s1
Molecular Formula | C46H56N4O10 |
Molecular Weight | 824.9576 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 8 / 9 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 14:59:52 UTC 2023
by
admin
on
Fri Dec 15 14:59:52 UTC 2023
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Record UNII |
5J49Q6B70F
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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WHO-VATC |
QL01CA02
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LIVERTOX |
1030
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NCI_THESAURUS |
C932
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WHO-ATC |
L01CA02
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WHO-ESSENTIAL MEDICINES LIST |
8.2
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NDF-RT |
N0000007780
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NDF-RT |
N0000007780
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NCI_THESAURUS |
C67422
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NDF-RT |
N0000175612
Created by
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Code System | Code | Type | Description | ||
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DB00541
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CHEMBL90555
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SUB00059MIG
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m11453
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DTXSID1032278
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1440
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2825
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200-318-1
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C933
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100000079089
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11202
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5388993
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5J49Q6B70F
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5J49Q6B70F
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57-22-7
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VINCRISTINE
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D014750
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6785
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3199
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143658
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Vincristine
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28445
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Related Record | Type | Details | ||
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METABOLIC ENZYME -> SUBSTRATE | |||
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METABOLIC ENZYME -> SUBSTRATE |
CYP3A5 was more efficient in catalyzing the formation of M1 compared with CYP3A4 (9- to 14-fold higher intrinsic clearance for CYP3A5).
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TRANSPORTER -> SUBSTRATE | |||
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TRANSPORTER -> INHIBITOR |
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TRANSPORTER -> INHIBITOR | |||
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TRANSPORTER -> SUBSTRATE | |||
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TRANSPORTER -> SUBSTRATE |
Dogs homozygous or heterozygous for the ABCB1-1Δ mutation are significantly more likely than normal dogs to develop haematological and gastrointestinal toxicity.
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TRANSPORTER -> SUBSTRATE |
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TARGET -> INHIBITOR | |||
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TRANSPORTER -> SUBSTRATE | |||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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METABOLITE -> PARENT |
MINOR
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Route of Elimination | PHARMACOKINETIC |
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Route of Elimination | PHARMACOKINETIC |
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Biological Half-life | PHARMACOKINETIC |
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