Details
Stereochemistry | ACHIRAL |
Molecular Formula | C15H12O |
Molecular Weight | 208.2552 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C(\C=C\C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=DQFBYFPFKXHELB-VAWYXSNFSA-N
InChI=1S/C15H12O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-12H/b12-11+
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Antioxidative function and substrate specificity of NAD(P)H-dependent alkenal/one oxidoreductase. A new role for leukotriene B4 12-hydroxydehydrogenase/15-oxoprostaglandin 13-reductase. | 2001 Nov 2 |
|
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
|
2-Hydroxychalcone and xanthohumol inhibit invasion of triple negative breast cancer cells. | 2013 May 25 |
Patents
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
210-383-8
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
ALTERNATIVE | |||
|
27618
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
48965
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
637760
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
5S5A2Q39HX
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
4523
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
614-47-1
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
167107
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
DTXSID8022531
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
202-330-2
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
2592960
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
94-41-7
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
NON-SPECIFIC STEREOCHEMISTRY | |||
|
m3306
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | Merck Index | ||
|
26612
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
CHALCONE
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
D002599
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY | |||
|
5S5A2Q39HX
Created by
admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
|
PRIMARY |
ACTIVE MOIETY