Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H8O2 |
| Molecular Weight | 160.1693 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC(O)=C2C=CC=CC2=C1
InChI
InChIKey=XOOMNEFVDUTJPP-UHFFFAOYSA-N
InChI=1S/C10H8O2/c11-8-5-7-3-1-2-4-9(7)10(12)6-8/h1-6,11-12H
| Molecular Formula | C10H8O2 |
| Molecular Weight | 160.1693 |
| 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 |
|---|---|---|
| Comparative developmental toxicity of environmentally relevant oxygenated PAHs. | 2013-09-01 |
|
| Electrophilic components of diesel exhaust particles (DEP) activate transient receptor potential ankyrin-1 (TRPA1): a probable mechanism of acute pulmonary toxicity for DEP. | 2011-06-20 |
|
| Functional characterization of the promiscuous prenyltransferase responsible for furaquinocin biosynthesis: identification of a physiological polyketide substrate and its prenylated reaction products. | 2010-12-17 |
|
| Carbon starved anther encodes a MYB domain protein that regulates sugar partitioning required for rice pollen development. | 2010-03 |
|
| Antibiotic pigment from desert soil actinomycetes; biological activity, purification and chemical screening. | 2009-09 |
|
| rac-(1S,2R)-Diethyl 6-hydr-oxy-1-(4-methoxy-phen-yl)-3-oxo-2,3-di-hydro-1H-benzo[f]chromen-2-yl]-phospho-nate. | 2008-06-07 |
|
| A soluble, magnesium-independent prenyltransferase catalyzes reverse and regular C-prenylations and O-prenylations of aromatic substrates. | 2007-06-26 |
|
| Effector-repressor interactions, binding of a single effector molecule to the operator-bound TtgR homodimer mediates derepression. | 2006-03-17 |
|
| Naphthalene-1,3-diol. | 2006-02 |
|
| Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products. | 2005-06-16 |
|
| Enantioselective DNA alkylation by a pyrrole-imidazole S-CBI conjugate. | 2004-07-28 |
|
| Selective nonpeptidic inhibitors of herpes simplex virus type 1 and human cytomegalovirus proteases. | 2001-03 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:15:52 GMT 2025
by
admin
on
Mon Mar 31 19:15:52 GMT 2025
|
| Record UNII |
5X457YEW8Y
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
205-079-7
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY | |||
|
C027029
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY | |||
|
8601
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY | |||
|
132-86-5
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY | |||
|
115890
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY | |||
|
DTXSID8059631
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY | |||
|
m7751
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY | Merck Index | ||
|
5X457YEW8Y
Created by
admin on Mon Mar 31 19:15:52 GMT 2025 , Edited by admin on Mon Mar 31 19:15:52 GMT 2025
|
PRIMARY |