Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C15H18O4 |
Molecular Weight | 262.301 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12C[C@@H](C)[C@]3([H])C=CC(=O)[C@@]3(C)[C@@H](O)[C@]1([H])C(=C)C(=O)O2
InChI
InChIKey=ZVLOPMNVFLSSAA-XEPQRQSNSA-N
InChI=1S/C15H18O4/c1-7-6-10-12(8(2)14(18)19-10)13(17)15(3)9(7)4-5-11(15)16/h4-5,7,9-10,12-13,17H,2,6H2,1,3H3/t7-,9+,10-,12-,13+,15+/m1/s1
Molecular Formula | C15H18O4 |
Molecular Weight | 262.301 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:44:05 UTC 2023
by
admin
on
Fri Dec 15 19:44:05 UTC 2023
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Record UNII |
4GUY9L896T
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Record Status |
Validated (UNII)
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Record Version |
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-
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Code | English |
Code System | Code | Type | Description | ||
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3490
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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23205
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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HELENALIN
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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C001329
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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85236
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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DTXSID50217868
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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4GUY9L896T
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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PRIMARY | |||
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6754-13-8
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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PRIMARY | |||
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m5931
Created by
admin on Fri Dec 15 19:44:05 UTC 2023 , Edited by admin on Fri Dec 15 19:44:05 UTC 2023
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PRIMARY | Merck Index |
Related Record | Type | Details | ||
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TARGET -> INHIBITOR |
Helenalin selectively alkylates p65 subunit at
Cys38 [27, 63]. Formation of this covalent bond sterically
prevents the p50/p65 heterodimer from binding to DNA and therefore inhibits its transcriptional activation.
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TARGET -> INHIBITOR |
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PARENT -> ACTIVE CONSTITUENT ALWAYS PRESENT |
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TARGET -> INHIBITOR |
Helenalin binds to Cys445 of telomerase
in the Michael-type addition reaction, disturbing recognition of the telomere DNA at the telomerase active site and causing suppression of the enzyme activity.
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PARENT -> ACTIVE CONSTITUENT ALWAYS PRESENT |
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