Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H14O2 |
| Molecular Weight | 166.217 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC1=CC=C(O)C=C1O
InChI
InChIKey=CSHZYWUPJWVTMQ-UHFFFAOYSA-N
InChI=1S/C10H14O2/c1-2-3-4-8-5-6-9(11)7-10(8)12/h5-7,11-12H,2-4H2,1H3
| Molecular Formula | C10H14O2 |
| Molecular Weight | 166.217 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL1973 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23205541 |
21.0 µM [IC50] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Quasi-drugs developed in Japan for the prevention or treatment of hyperpigmentary disorders. | 2010-06-18 |
|
| Efficacy and safety of liposome-encapsulated 4-n-butylresorcinol 0.1% cream for the treatment of melasma: a randomized controlled split-face trial. | 2010-04 |
|
| The Efficacy and Safety of 4-n-butylresorcinol 0.1% Cream for the Treatment of Melasma: A Randomized Controlled Split-face Trial. | 2010-02 |
|
| Studies on depigmenting activities of dihydroxyl benzamide derivatives containing adamantane moiety. | 2009-03-01 |
|
| Evaluation of efficacy and safety of rucinol serum in patients with melasma: a randomized controlled trial. | 2007-05 |
|
| Inhibitory effects of 4-n-butylresorcinol on tyrosinase activity and melanin synthesis. | 2005-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:34:17 GMT 2025
by
admin
on
Mon Mar 31 19:34:17 GMT 2025
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| Record UNII |
2IK4UQ3ZGA
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| Record Status |
Validated (UNII)
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| Record Version |
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2IK4UQ3ZGA
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DTXSID50172403
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18979-61-8
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1600929
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2IK4UQ3ZGA
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300000051566
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4-Butylresorcinol
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205912
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