Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H16N2O4 |
Molecular Weight | 348.352 |
Optical Activity | ( + ) |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[C@@]1(O)C(=O)OCC2=C1C=C3N(CC4=C3N=C5C=CC=CC5=C4)C2=O
InChI
InChIKey=VSJKWCGYPAHWDS-FQEVSTJZSA-N
InChI=1S/C20H16N2O4/c1-2-20(25)14-8-16-17-12(7-11-5-3-4-6-15(11)21-17)9-22(16)18(23)13(14)10-26-19(20)24/h3-8,25H,2,9-10H2,1H3/t20-/m0/s1
Molecular Formula | C20H16N2O4 |
Molecular Weight | 348.352 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:45:30 UTC 2023
by
admin
on
Fri Dec 15 15:45:30 UTC 2023
|
Record UNII |
XT3Z54Z28A
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C1904
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
24360
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
C338
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
SUB25812
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
DTXSID0030956
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
DB04690
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
27656
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
94600
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
1672280
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
D002166
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
m3007
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | Merck Index | ||
|
100000089959
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
7689-03-4
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
CAMPTOTHECIN
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY | |||
|
XT3Z54Z28A
Created by
admin on Fri Dec 15 15:45:30 UTC 2023 , Edited by admin on Fri Dec 15 15:45:30 UTC 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
SALT/SOLVATE -> PARENT | |||
|
DERIVATIVE -> PARENT |
|
||
|
TRANSPORTER -> SUBSTRATE |
Down-regulation of ABCB5αresulted in a gain of drug sensitivity to camptothecin 10-OH, 5-fluorouracil, and mitoxantrone.
|
||
|
CONJUGATE->CONJUGATE COMPONENT |
|
||
|
DERIVATIVE -> PARENT |
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |