SCHEMBL5013940

SCHEMBL5013940

Cc1c(Cc2cc(O)c(O)c(O)c2C)cc(O)c(O)c1O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 4/20 0.50
PRKCE Q02156 3/20 0.43
MYLK Q15746 2/20 0.43
MEN1 O00255 2/20 0.43
ALDH1A1 P00352 2/20 0.43
MAPT P10636 2/20 0.43
KMT2A Q03164 2/20 0.43
TDP1 Q9NUW8 2/20 0.43
PRKCG P05129 1/20 0.43
PRKCA P17252 1/20 0.43
APEX1 P27695 1/20 0.43
RECQL P46063 1/20 0.43
HSPA5 P11021 2/20 0.42
AMY1A P0DUB6 1/20 0.42
SELL P14151 1/20 0.42
SELP P16109 1/20 0.42
SELE P16581 1/20 0.42
CA1 P00915 2/20 0.41
CA2 P00918 2/20 0.41
CYP2C9 P11712 2/20 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
SCHEMBL278609 0.84 ALOX5 (0.49) MEN1MAPTKMT2ATDP1
SCHEMBL2221249 0.83 ALOX15 (0.43) PTPN1PRKCEMYLKMEN1ALDH1A1
SCHEMBL278588 0.82 BCL2 (0.62) PTPN1MEN1KMT2AHIF1AHSD17B10
SCHEMBL9059697 0.80 HSPA5 (0.47) PTPN1PRKCEMYLKMEN1ALDH1A1
SCHEMBL5532933 0.79 HMGCR (0.42) PTPN1PRKCEMYLKMEN1ALDH1A1
SCHEMBL8072029 0.76 GABRA1 (0.46) PRKCEMYLKMEN1ALDH1A1MAPT
SCHEMBL10743686 0.74 TYR (0.56) MEN1MAPTKMT2ATDP1
SCHEMBL5517885 0.73 TYR (0.59) MEN1MAPTKMT2ATDP1
SCHEMBL2220478 0.73 SELL (0.50) PRKCEMYLKMEN1ALDH1A1MAPT
Propane SCHEMBL2218962 0.72 SELL (0.43) PRKCEMYLKMEN1ALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4387152-A Light-sensitive mixture and copying material prepared therefrom, and process for the preparation of a printing form from the copying material HOECHST AKTIENGESELLSCHAFT (DE) 1983-06-07 US claimed
JP-8311141-A None JP disclosed
US-20080070086-A1 Phase-Separated Polymer Electrolyte Membrane, Electrode - Phase-Separated Polymer Electrolyte Membrane Joint Using Same, Method for Manufacture Thereof, and Fuel Cell Using Same HITACHI CHEMICAL COMPANY, LTD. (JP) 2008-03-20 US disclosed
EP-1845573-A1 PHASE SEPARATION TYPE POLYMER ELECTROLYTE FILM, ELECTRODE/PHASE SEPARATION TYPE POLYMER ELECTROLYTE FILM ASSEMBLY EMPLOYING THE SAME, PROCESSES FOR PRODUCING THE SAME, AND FUEL CELL EMPLOYING THE SAME Hitachi Chemical Co., Ltd. (JP) 2007-10-17 EP disclosed
EP-1352888-B1 Hydroxymethyl-substituted polyfunctional phenols HONSHU CHEMICAL IND (JP) 2007-06-13 EP disclosed
US-6906226-B2 Hydroxymethyl-substituted polyfunctional phenols HONSHU CHEMICAL INDUSTRY CO., LTD. (JP) 2005-06-14 US disclosed
US-6906130-B2 Inverted novolac resin-type insulation binder GEORGIA-PACIFIC RESINS, INC. (US) 2005-06-14 US disclosed
US-20040082713-A1 Inverted novolac resin-type insulation binder GEORGIA-PACIFIC RESINS, INC. 2004-04-29 US disclosed
US-20030204117-A1 Hydroxymethyl-substituted polyfunctional phenols HONSHU, CHEMICAL INDUSTRY CO., LTD. (JP) 2003-10-30 US disclosed
EP-1352888-A1 Hydroxymethyl-substituted polyfunctional phenols Honshu Chemical Industry Co., Ltd. (JP) 2003-10-15 EP disclosed
JP-H08311141-A RESOL TYPE PHENOLIC RESIN AND COATING THEREFROM KISHIMOTO AKIRA 1996-11-26 JP disclosed
US-5371140-A Catalytic polymerization of phenol-formaldehyde using alkali metal base as catalyst and urea as free aldehyde scavanger; scavanging, neutralizing basic catalyst GEORGIA-PACIFIC RESINS, INC. (US) 1994-12-06 US disclosed
US-4028367-A REACTING PHENOL WITH FORMALDEHYDE, DIHYDROXYDIPHENYLMETHANES PRESENT TO INHIBIT CRYSTAL FORMATION MONSANTO COMPANY (US) 1977-06-07 US disclosed
US-3956205-A High efficiency aqueous resole solutions being stable to crystallization and emulsifiable with method of manufacture MONSANTO COMPANY (US) 1976-05-11 US 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-20030204117-A1 Hydroxymethyl-substituted polyfunctional phenols TET1, TET3, TET2 PTPN1 1364/4885PRKCE 4760/4885MYLK 4159/4885

“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.