Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C28H22O6 |
Molecular Weight | 454.4707 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@H]1CC2=C(O[C@@H]1C3=CC4=C(OC(O4)(C5=CC=CC=C5)C6=CC=CC=C6)C=C3)C=C(O)C=C2O
InChI
InChIKey=NGJOOUAZHCZCOW-WNCULLNHSA-N
InChI=1S/C28H22O6/c29-20-14-22(30)21-16-23(31)27(32-25(21)15-20)17-11-12-24-26(13-17)34-28(33-24,18-7-3-1-4-8-18)19-9-5-2-6-10-19/h1-15,23,27,29-31H,16H2/t23-,27+/m0/s1
Molecular Formula | C28H22O6 |
Molecular Weight | 454.4707 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/2872863 |
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2872863 |
Bencianol (ZY 15051) possesses an anti-spasmogenic effect. It anticonstrictor properties in pial arteries in situ were studied. However, the information about the nowadays use of this compound is not available.
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3959160
The pretreatment with Bencianol (10(-10) M-10(-7) M) produced cytoprotective effects against CCl4 induced cell injury
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:03:06 GMT 2023
by
admin
on
Fri Dec 15 16:03:06 GMT 2023
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Record UNII |
C4A4TVM56F
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29698
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C4A4TVM56F
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C73228
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287-240-1
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SUB05702MIG
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C047756
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ACTIVE MOIETY |