Phenylethyl Alcohol

Phenylethyl Alcohol

SCHEMBL183529

CC(=O)O.OCCc1ccccc1

nearest known ligand 0.76

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Phenylethyl Alcohol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 2/20 0.76
ALDH1A1 P00352 3/20 0.61
KEAP1 Q14145 1/20 0.54
SMN1; SMN2 Q16637 2/20 0.50
HDAC2 Q92769 2/20 0.50
HDAC8 Q9BY41 2/20 0.50
HDAC6 Q9UBN7 2/20 0.50
HDAC3 O15379 1/20 0.50
MAPK1 P28482 1/20 0.50
ADRA1A P35348 1/20 0.50
HDAC4 P56524 1/20 0.50
SLC6A3 Q01959 1/20 0.50
HDAC1 Q13547 1/20 0.50
HDAC7 Q8WUI4 1/20 0.50
HDAC10 Q969S8 1/20 0.50
HDAC11 Q96DB2 1/20 0.50
HDAC9 Q9UKV0 1/20 0.50
HDAC5 Q9UQL6 1/20 0.50
FFAR1 O14842 1/20 0.50
CYP4F2 P78329 2/20 0.48

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Phenylethyl Alcohol SCHEMBL28312218 0.91 TDP1 (0.70) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2
Phenylethyl Alcohol SCHEMBL28145944 0.91 TDP1 (0.70) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2
Phenylethyl Alcohol SCHEMBL28920276 0.89 TDP1 (0.67) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2
Phenylethyl Alcohol SCHEMBL10904935 0.87 TDP1 (0.89) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2
Acetic Acid SCHEMBL7431776 0.87 ALDH1A1 (0.70) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2
Phenylethyl Alcohol SCHEMBL1867158 0.87 TDP1 (1.00) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2
Phenylethyl Alcohol SCHEMBL8968173 0.87 TDP1 (1.00) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2
Phenylethyl Alcohol SCHEMBL1838 0.87
Acetophenone SCHEMBL8048362 0.87 TDP1 (0.64) TDP1ALDH1A1KEAP1SMN1; SMN2CYP4F2
Phenylethyl Alcohol SCHEMBL11450063 0.87 TDP1 (1.00) TDP1ALDH1A1KEAP1SMN1; SMN2HDAC2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 286 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111830145-B Method for determining feeding ratio and distillation time of black-branch rose hydrosol 北京市农林科学院 2022-11-11 CN claimed
CN-108853105-A Cosmetic composition, composite medicine and food compositions 西姆莱斯股份公司 2018-11-23 CN claimed
EP-1476534-B1 \"DOUBLESSE\" METHOD FOR PRODUCING SPARKLING WINE SEKTKELLEREI SCHLOSS WACHENHEI (DE) 2005-06-29 EP claimed
WO-2001060986-A9 ESTERASE ENZYMES HAVING SELECTIVE ACTIVITY THERMOGEN INC (US) 2002-10-17 WO claimed
WO-2001060986-A2 ESTERASE ENZYMES HAVING SELECTIVE ACTIVITY THERMOGEN, INC. (US) 2001-08-23 WO claimed
CN-119677494-A Flavored composition comprising at least one sulfur-containing antioxidant compound, at least one organic UV screening agent and at least one flavoring substance 莱雅公司 2025-03-21 CN disclosed
EP-4330853-A1 SYSTEMS AND METHODS FOR CHEMICAL AND BIOLOGICAL AUTHENTICATION Salvus, LLC (US) 2024-03-06 EP disclosed
EP-2646533-B2 FABRIC CONDITIONERS UNILEVER IP HOLDINGS B V (NL) 2023-07-05 EP disclosed
EP-3310164-B1 METHOD AND SYSTEM FOR ATTRACTING LEPIDOPTEROUS INSECTS THE NEW ZEALAND INSTITUTE FOR PLANT AND FOOD RESEACH LTD (NZ) 2023-06-07 EP disclosed
CN-115836061-A Odorants and compositions comprising odorants 丝趣科尔卡有限公司 2023-03-21 CN disclosed
CN-110079466-B Yeast and application thereof in fermentation of lotus seed wine 中国石油大学(华东) 2023-01-10 CN disclosed
CN-110079466-B Yeast and application thereof in fermentation of lotus seed wine 中国石油大学(华东) 2023-01-10 CN disclosed
WO-2006133592-A1 CYCLOAKYLIDENE- (ORTHO SUBSTITUTED PHENYL) -ACETONITRILES AND THEIR USE AS ODORANTS GIVAUDAN SA (CH) 2006-12-21 WO disclosed
CN-1144779-C Process for preparing alkylphenylethyl aminopropanediol and intermediate obtained therein 杭州中美华东制药有限公司 2004-04-07 CN disclosed
WO-2001060986-A9 ESTERASE ENZYMES HAVING SELECTIVE ACTIVITY THERMOGEN INC (US) 2002-10-17 WO disclosed
WO-2001060986-A2 ESTERASE ENZYMES HAVING SELECTIVE ACTIVITY THERMOGEN, INC. (US) 2001-08-23 WO disclosed
EP-1115487-A1 SUPPORTED BF3-COMPLEX SOLID ACID CATALYST, PREPARATION AND USE THE UNIVERSITY OF YORK (GB) 2001-07-18 EP disclosed
CN-1266844-A Process for preparing alkylphenylethyl aminopropanediol and intermediate obtained therein CHINA AMERICA JOINT HUADONG PH (CN) 2000-09-20 CN disclosed
WO-2000013792-A1 SUPPORTED BF3-COMPLEX SOLID ACID CATALYST, PREPARATION AND USE THE UNIVERSITY OF YORK (GB) 2000-03-16 WO disclosed
US-5552380-A Perfume uses of phenyl alkanol derivatives INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) 1996-09-03 US disclosed