Salicyl Alcohol

Salicyl Alcohol

SCHEMBL4149772

CC(=O)O.OCc1ccccc1O

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Salicyl 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
AKR1B1 P15121 1/20 0.59
PKM P14618 2/20 0.50
HSPA5 P11021 1/20 0.50
HIF1A Q16665 2/20 0.45
CYP2D6 P10635 1/20 0.45
TSHR P16473 1/20 0.45
IAPP P10997 1/20 0.44
TAAR1 Q96RJ0 1/20 0.43
PDCD1 Q15116 1/20 0.42
CD274 Q9NZQ7 1/20 0.42
CA12 O43570 2/20 0.42
CA2 P00918 2/20 0.42
IDO1 P14902 1/20 0.42
HPGD P15428 2/20 0.42
LMNA P02545 1/20 0.42
GAA P10253 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
THRB P10828 1/20 0.41
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41

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
Salicyl Alcohol SCHEMBL1395496 0.91 AKR1B1 (0.64) AKR1B1PKMHSPA5HIF1ACYP2D6
Salicyl Alcohol SCHEMBL28230169 0.89 HSPA5 (0.62) AKR1B1PKMHSPA5HIF1ACYP2D6
Salicyl Alcohol SCHEMBL9577921 0.88 AKR1B1 (0.52) AKR1B1PKMHSPA5HIF1ACYP2D6
Salicyl Alcohol SCHEMBL29728553 0.87 AKR1B1 (0.59) AKR1B1PKMHSPA5HIF1ACYP2D6
Salicyl Alcohol SCHEMBL9220390 0.86 HSPA5 (0.59) AKR1B1HSPA5HIF1ACYP2D6TSHR
Salicyl Alcohol SCHEMBL29453973 0.86
Salicyl Alcohol SCHEMBL17028795 0.86 HSPA5 (0.65) AKR1B1HSPA5HIF1ACYP2D6TSHR
Salicyl Alcohol SCHEMBL15639 0.86
Salicyl Alcohol SCHEMBL16965609 0.86 AKR1B1 (0.53) AKR1B1PKMHSPA5HIF1ACYP2D6
Acetic Acid SCHEMBL27895243 0.84 AKR1B1 (0.61) AKR1B1HSPA5HIF1ACYP2D6TSHR

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101974436-B Lignocellulose degrading bacteria and application thereof INST AGRI RESOURCES CAAS 2012-10-03 CN disclosed
CN-101104745-B Method for producing natural blue pigment UNIV EAST CHINA SCIENCE & TECH 2011-05-18 CN disclosed
CN-101974436-A Lignocellulose degrading bacteria and application thereof INST AGRI RESOURCES CAAS 2011-02-16 CN disclosed
CN-101225404-B Compound organic nitrogen source used for microbial fermentation UNIV EAST CHINA SCIENCE & TECH 2010-12-29 CN disclosed
US-20090068273-A1 Inhalation devices for delivering phenethanolamine derivatives for the treatment of respiratory diseases GLAXO GROUP LIMITED (GB) 2009-03-12 US disclosed
CN-101225404-A Compound organic nitrogen source used for microbial fermentation UNIV EAST CHINA SCIENCE & TECH (CN) 2008-07-23 CN disclosed
CN-101104745-A Method for producing natural blue pigment UNIV EAST CHINA SCIENCE & TECH (CN) 2008-01-16 CN disclosed
EP-1497261-A1 PHENETHANOLAMINE DERIVATIVES GLAXO GROUP LIMITED (GB) 2005-01-19 EP disclosed
EP-1425001-A1 PHENETHANOLAMINE DERIVATIVES FOR TREATMENT OF RESPIRATORY DISEASES GLAXO GROUP LIMITED (GB) 2004-06-09 EP disclosed
WO-2003091204-A1 PHENETHANOLAMINE DERIVATIVES GLAXO GROUP LIMITED (GB) 2003-11-06 WO disclosed
WO-2003024439-A1 PHENETHANOLAMINE DERIVATIVES FOR TREATMENT OF RESPIRATORY DISEASES GLAXO GROUP LIMITED (GB) 2003-03-27 WO disclosed
EP-0377308-B1 Phenolic resins BORDEN UK LTD (GB) 1993-11-03 EP disclosed
US-5051454-A An esterified phenolic compound, an unesterified phenolic resole and a base and curing BORDEN, INC. (US) 1991-09-24 US disclosed
EP-0377308-A1 Phenolic resins BORDEN (UK) LIMITED (GB) 1990-07-11 EP disclosed
WO-1990006904-A2 PHENOLIC RESINS BORDEN (UK) LIMITED (GB) 1990-06-28 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090068273-A1 Inhalation devices for delivering phenethanolamine derivatives for the treatment of respiratory diseases PNMT, CHRM3, HRH4 AKR1B1 2819/4885PKM 1267/4885HSPA5 522/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.