Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H16 |
| Molecular Weight | 208.2982 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C=C(CCC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=PWSZACWUDDFZMQ-UHFFFAOYSA-N
InChI=1S/C16H16/c1-14(16-10-6-3-7-11-16)12-13-15-8-4-2-5-9-15/h2-11H,1,12-13H2
| Molecular Formula | C16H16 |
| Molecular Weight | 208.2982 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006-11 |
|
| Estrogenic activity of styrene oligomers after metabolic activation by rat liver microsomes. | 2003-03 |
|
| Certain styrene oligomers have proliferative activity on MCF-7 human breast tumor cells and binding affinity for human estrogen receptor. | 2001-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:37:24 GMT 2025
by
admin
on
Mon Mar 31 20:37:24 GMT 2025
|
| Record UNII |
557SU9B24T
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
519286
Created by
admin on Mon Mar 31 20:37:24 GMT 2025 , Edited by admin on Mon Mar 31 20:37:24 GMT 2025
|
PRIMARY | |||
|
557SU9B24T
Created by
admin on Mon Mar 31 20:37:24 GMT 2025 , Edited by admin on Mon Mar 31 20:37:24 GMT 2025
|
PRIMARY | |||
|
16606-47-6
Created by
admin on Mon Mar 31 20:37:24 GMT 2025 , Edited by admin on Mon Mar 31 20:37:24 GMT 2025
|
PRIMARY | |||
|
DTXSID50168068
Created by
admin on Mon Mar 31 20:37:24 GMT 2025 , Edited by admin on Mon Mar 31 20:37:24 GMT 2025
|
PRIMARY |