Alcohol

Alcohol

SCHEMBL6231697

CCCCCCCC/C=C/C=C/O.CCO

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of 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
FASN P49327 1/20 0.55
ALDH1A1 P00352 1/20 0.52
TSHR P16473 1/20 0.52
FAAH O00519 4/20 0.46
KDM4E B2RXH2 1/20 0.46
TRPV1 Q8NER1 1/20 0.45
TERT O14746 2/20 0.44
GMNN O75496 1/20 0.44
USP2 O75604 1/20 0.44
LMNA P02545 1/20 0.44
CYP1A2 P05177 1/20 0.44
POLB P06746 1/20 0.44
MAPT P10636 1/20 0.44
CYP2C9 P11712 1/20 0.44
ALOX15 P16050 1/20 0.44
APEX1 P27695 1/20 0.44
CYP2C19 P33261 1/20 0.44
RECQL P46063 1/20 0.44
BLM P54132 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44

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
Alcohol SCHEMBL346159 0.98 ALDH1A1 (0.55) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL149569 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL10955534 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL8102518 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL356416 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL317072 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL317433 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL10814643 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL7293653 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E
SCHEMBL3252003 0.96 FASN (0.59) FASNALDH1A1TSHRFAAHKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050271735-A1 Method of encapsulating hydrophobic organic molecules in polyurea capsules MCMASTER UNIVERSITY (CA) 2005-12-08 US claimed
EP-1517746-A1 METHOD OF ENCAPSULATING HYDROPHOBIC ORGANIC MOLECULES IN POLYUREA CAPSULES McMaster University (CA) 2005-03-30 EP claimed
WO-2003101606-A1 METHOD OF ENCAPSULATING HYDROPHOBIC ORGANIC MOLECULES IN POLYUREA CAPSULES MCMASTER UNIVERSITY (CA) 2003-12-11 WO claimed
US-20050271735-A1 Method of encapsulating hydrophobic organic molecules in polyurea capsules MCMASTER UNIVERSITY (CA) 2005-12-08 US disclosed
EP-1517746-A1 METHOD OF ENCAPSULATING HYDROPHOBIC ORGANIC MOLECULES IN POLYUREA CAPSULES McMaster University (CA) 2005-03-30 EP disclosed
WO-2003101606-A1 METHOD OF ENCAPSULATING HYDROPHOBIC ORGANIC MOLECULES IN POLYUREA CAPSULES MCMASTER UNIVERSITY (CA) 2003-12-11 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-20050271735-A1 Method of encapsulating hydrophobic organic molecules in polyurea capsules PUF60, HNRNPU, HNRNPUL1 FASN 463/4885ALDH1A1 1938/4885TSHR 2960/4885

“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.