Alcohol

Alcohol

SCHEMBL4094172

CCO.O=[N+]([O-])c1ccc(CC(O)c2cccc(C3OCCO3)n2)cc1

nearest known ligand 0.37

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 18)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 1/20 0.37
CCR3 P51677 5/20 0.36
MEN1 O00255 2/20 0.35
KMT2A Q03164 2/20 0.35
DRD4 P21917 1/20 0.35
TSHR P16473 1/20 0.35
LMNA P02545 1/20 0.34
HTR2A P28223 1/20 0.34
HTR1D P28221 1/20 0.34
HTR7 P34969 1/20 0.34
HTR2B P41595 1/20 0.34
NPC1 O15118 2/20 0.33
LOXL2 Q9Y4K0 1/20 0.33
CXCR3 P49682 1/20 0.33
TP53 P04637 1/20 0.33
RAB9A P51151 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
KDM4E B2RXH2 1/20 0.33

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
SCHEMBL9906217 0.96 CCR3 (0.39) EPHX1CCR3MEN1KMT2ATSHR
SCHEMBL4094176 0.79 MAPT (0.37) EPHX1MEN1KMT2ATSHRLMNA
SCHEMBL9906216 0.74 TSHR (0.43) EPHX1CCR3MEN1KMT2ATSHR
SCHEMBL13722427 0.71 LMNA (0.42) CCR3MEN1KMT2ATSHRLMNA
Alcohol SCHEMBL4097978 0.69 ALDH1A1 (0.40) EPHX1MEN1KMT2ADRD4TSHR
SCHEMBL8541579 0.68 KMT2A (0.49) MEN1KMT2ATSHRNPC1TP53
SCHEMBL6984191 0.66 CHRNA7 (0.43) DRD4
SCHEMBL25189836 0.64 ALDH1A1 (0.44) MEN1KMT2ANPC1RAB9ASMN1; SMN2
Alcohol SCHEMBL28329576 0.64 TSHR (0.61) TSHRLMNALOXL2
SCHEMBL10621456 0.63 LMNA (0.50) EPHX1MEN1KMT2ATSHRLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2004642-B1 BIFUNCTIONAL POLYAZAMACROCYCLIC CHELATING AGENTS Nordion (Canada) Inc (CA) 2017-07-26 EP disclosed
US-8518715-B2 Bifunctional polyazamacrocyclic chelating agents NORDION (CANADA) INC. (CA) 2013-08-27 US disclosed
US-20120276001-A1 BIFUNCTIONAL POLYAZAMACROCYCLIC CHELATING AGENTS Nordion (Canada) Inc (CA) 2012-11-01 US disclosed
US-8198101-B2 Bifunctional polyazamacrocyclic chelating agents NORDION (CANADA) INC. (CA) 2012-06-12 US disclosed
US-20090202521-A1 Bifunctional Polyazamacrocyclic Chelating Agents MDS (CANADA) INC. (CA) 2009-08-13 US disclosed
EP-2004642-A1 BIFUNCTIONAL POLYAZAMACROCYCLIC CHELATING AGENTS MDS (Canada) Inc. (CA) 2008-12-24 EP disclosed
WO-2007104135-A1 BIFUNCTIONAL POLYAZAMACROCYCLIC CHELATING AGENTS MDS (CANADA) INC. (CA) 2007-09-20 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 (2 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-20090202521-A1 Bifunctional Polyazamacrocyclic Chelating Agents LPXN, FCGRT, POLQ EPHX1 4043/4885CCR3 1142/4885MEN1 691/4885
US-20120276001-A1 BIFUNCTIONAL POLYAZAMACROCYCLIC CHELATING AGENTS LPXN, FCGRT, F13A1 EPHX1 3965/4885CCR3 1242/4885MEN1 497/4885

“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.