Cinnamic Alcohol

Cinnamic Alcohol

SCHEMBL901221

CCO.OC/C=C/c1ccccc1

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
PAM P19021 1/20 0.52
HTR2A P28223 3/20 0.48
IDO1 P14902 2/20 0.47
ALDH1A1 P00352 1/20 0.45
CYP3A4 P08684 1/20 0.45
RECQL P46063 1/20 0.45
NPC1 O15118 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
MAOB P27338 2/20 0.44
RELA Q04206 1/20 0.44
GLA P06280 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
NFE2L2 Q16236 1/20 0.43
SIGMAR1 Q99720 1/20 0.43

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
Cinnamic Alcohol SCHEMBL28289701 1.00 PAM (0.52) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL39220 0.93 PAM (0.58) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL28583889 0.93 PAM (0.58) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL891462 0.93 PAM (0.58) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL39219 0.93 PAM (0.58) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL4175503 0.93 PAM (0.58) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL27887623 0.93 PAM (0.58) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL28671092 0.91 PAM (0.56) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL28671087 0.91 PAM (0.56) PAMHTR2AIDO1ALDH1A1CYP3A4
Cinnamic Alcohol SCHEMBL27879151 0.91 PAM (0.56) PAMHTR2AIDO1ALDH1A1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111424006-B Recombinant cell and application thereof in synthesizing alpha, beta-unsaturated aldehyde 浙江工业大学 2022-04-19 CN disclosed
US-11062794-B2 Olfactory signature and odorant mixture having the same YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2021-07-13 US disclosed
CN-111424006-A Recombinant cell and application thereof in synthesizing α -unsaturated aldehyde 浙江工业大学 2020-07-17 CN disclosed
US-20180253534-A1 OLFACTORY SIGNATURE AND ODORANT MIXTURE HAVING THE SAME YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2018-09-06 US disclosed
EP-3365418-A2 PARTICLES FOR MALODOR REDUCTION The Procter and Gamble Company (US) 2018-08-29 EP disclosed
EP-3325022-A1 WATER-BASED FRAGRANCE COMPOSITION, FRAGRANCE DELIVERY DEVICE, AND METHOD OF PROVIDING A LONG-LASTING SCENT S.C. Johnson & Son, Inc. (US) 2018-05-30 EP disclosed
EP-3307394-A1 FRAGRANCE FIXATIVES AND COMPOSITIONS COMPRISING THEREOF The Procter and Gamble Company (US) 2018-04-18 EP disclosed
EP-3307231-A1 FRAGRANCE COMPOSITIONS AND USES THEREOF The Procter and Gamble Company (US) 2018-04-18 EP disclosed
EP-3307393-A1 FRAGRANCE COMPOSITION The Procter and Gamble Company (US) 2018-04-18 EP disclosed
WO-2017158497-A1 HYDROPHOBICALLY MODIFIED UREA ETHERS AS STRUCTURANTS FOR HYDROPHOBIC SYSTEMS PROCTER & GAMBLE INERNATIONAL OPERATIONS SA (CH) 2017-09-21 WO disclosed
US-20100104525-A1 USE OF FRAGRANCE COMPOSITIONS FOR THE PREVENTION OF THE DEVELOPMENT OF INDOLE BASE MALODOURS FROM FECAL AND URINE BASED SOILS TAKASAGO INTERNATIONAL CORPORATION (JP) 2010-04-29 US disclosed
WO-2009117621-A1 PEST CONTROL COMPOSITIONS AND METHODS TYRATECH, INC. (US) 2009-09-24 WO disclosed
US-20080032912-A1 Use of fragrance compositions for the prevention of the development of indole base malodours from fecal and urine based soils TAKASAGO INTERNATIONAL CORPORATION (JP) 2008-02-07 US disclosed
EP-1884251-A1 Use of fragrance compositions for the prevention of the development of indole based malodours from faecal and urine based soils Takasago International Corporation (JP) 2008-02-06 EP disclosed
EP-1622915-A1 FRAGRANCE COMPOSITIONS COMPRISING BENZO [4,5]THIENO[3,2-B] PYRAN-2-ONE Flexitral, Inc. (US) 2006-02-08 EP disclosed
WO-2004092182-A1 FRAGRANCE COMPOSITIONS COMPRISING BENZO[4,5]THIENO[3,2-B]PYRAN-2-ONE FLEXITRAL, INC. (US) 2004-10-28 WO disclosed
EP-1458666-A1 IMPROVED AROMACHEMICALS Flexitral Inc. (US) 2004-09-22 EP disclosed
WO-2003053887-A1 A METHOD FOR INCREASING THE STABILITY AND INTENSITY OF ODORANT MOLECULES FLEXITRAL, INC. (US) 2003-07-03 WO disclosed
WO-2003053902-A1 IMPROVED AROMACHEMICALS FLEXITRAL, INC. (US) 2003-07-03 WO disclosed
US-5129951-A Exposure to benzaldehyde, salicylaldehyde, cinnamaldehyde, hydrocinnamaldehyde, thymol THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF AGRICULTURE (US) 1992-07-14 US disclosed