SCHEMBL7189135

SCHEMBL7189135

CC(C)(C)Sc1ccccc1O

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.44
TSHR P16473 3/20 0.44
TDP1 Q9NUW8 2/20 0.44
ALOX15 P16050 3/20 0.41
HPGD P15428 3/20 0.41
CA2 P00918 2/20 0.41
NPC1 O15118 2/20 0.41
LMNA P02545 2/20 0.41
CYP3A4 P08684 2/20 0.41
MAPT P10636 2/20 0.41
HSD17B10 Q99714 2/20 0.41
KDM4E B2RXH2 1/20 0.41
CA12 O43570 1/20 0.41
GMNN O75496 1/20 0.41
EGFR P00533 1/20 0.41
FYN P06241 1/20 0.41
POLB P06746 1/20 0.41
CA3 P07451 1/20 0.41
MMP9 P14780 1/20 0.41
NFKB1 P19838 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
SCHEMBL6934720 0.82 AOC3 (0.37) ALDH1A1TSHRTDP1HPGDMAPT
SCHEMBL15988650 0.79 TSHR (0.39) ALDH1A1TSHRTDP1ALOX15HPGD
SCHEMBL1275601 0.78 GABRA1 (0.42) ALDH1A1TSHRTDP1ALOX15HPGD
SCHEMBL16710910 0.77 ALDH1A1 (0.41) ALDH1A1TSHRTDP1ALOX15HPGD
SCHEMBL30821022 0.77 KIF11 (0.38) ALDH1A1TSHRTDP1ALOX15HPGD
SCHEMBL3542339 0.76 ALDH1A1 (0.41) ALDH1A1TSHRTDP1ALOX15HPGD
SCHEMBL29788344 0.76 ALDH1A1 (0.41) ALDH1A1TSHRTDP1ALOX15HPGD
SCHEMBL7930508 0.73 ACHE (0.43) ALDH1A1TSHRTDP1CA2CYP3A4
SCHEMBL7189127 0.73 CETP (0.34) ALDH1A1HPGDCA2CA12CA4
SCHEMBL5050103 0.73 ENPP2 (0.39) MAPTCA4CA5ACA14CA5B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0220660-B1 SEMI-PERMEABLES MEMBRANES PREPARED VIA REACTION OF CATIONIC GROUPS WITH NUCLEOPHILIC GROUPS THE DOW CHEMICAL COMPANY (US) 1992-03-11 EP claimed
US-4704324-A REVERSE OSMOSIS, GAS SEPARATION, ULTRAFILTRATION THE DOW CHEMICAL COMPANY (US) 1987-11-03 US claimed
WO-1987002682-A1 SEMI-PERMEABLE MEMBRANES PREPARED VIA REACTION OF CATIONIC GROUPS WITH NUCLEOPHILIC GROUPS THE DOW CHEMICAL COMPANY (US) 1987-05-07 WO claimed
EP-0220660-A2 Semi-permeables membranes prepared via reaction of cationic groups with nucleophilic groups THE DOW CHEMICAL COMPANY (US) 1987-05-06 EP claimed
US-10927076-B2 HSP90B N-terminal isoform-selective inhibitors UNIVERSITY OF KANSAS (US) 2021-02-23 US disclosed
US-6627714-B2 Copolymerizing ethylene and dicyclopentadiene or tricyclopentadiene, and cyclic olefin in presence of metallocene catalyst to produce copolymer MARUZEN PETROCHEMICAL CO., LTD. (JP) 2003-09-30 US disclosed
CN-1097588-C Dihydrobenzofuran and related compounds useful as anti-inflammatory agents UNIV FANDBILT (US) 2003-01-01 CN disclosed
US-20020058767-A1 Method for producing an olefin type copolymer having a cyclic structure MARUZEN PETROCHEMICAL CO., LTD. (JP) 2002-05-16 US disclosed
EP-1205497-A2 Method for producing an olefin type copolymer having a cyclic structure MARUZEN PETROCHEMICAL CO., LTD. (JP) 2002-05-15 EP disclosed
CN-1210529-A Dihydrobenzofuran and related compounds useful as anti-inflammatory agents PROCTER & GAMBLE (US) 1999-03-10 CN disclosed
EP-0220660-B1 SEMI-PERMEABLES MEMBRANES PREPARED VIA REACTION OF CATIONIC GROUPS WITH NUCLEOPHILIC GROUPS THE DOW CHEMICAL COMPANY (US) 1992-03-11 EP disclosed
EP-0253985-B1 STABILIZED MOULDING COMPOSITIONS BASED ON POLYVINYL CHLORIDE OR VINYL CHLORIDE COPOLYMERS AND STABILIZER SYSTEM HÜLS AKTIENGESELLSCHAFT (DE) 1991-12-27 EP disclosed
US-4839203-A COVALENT BONDING PRODUCING A COMPOSITE THE DOW CHEMICAL COMPANY (US) 1989-06-13 US disclosed
US-4797187-A COACERVATION OF CATIONS THE DOW CHEMICAL COMPANY (US) 1989-01-10 US disclosed
EP-0253985-A2 Stabilized moulding compositions based on polyvinyl chloride or vinyl chloride copolymers and stabilizer system HÜLS AKTIENGESELLSCHAFT (DE) 1988-01-27 EP disclosed
US-4704324-A REVERSE OSMOSIS, GAS SEPARATION, ULTRAFILTRATION THE DOW CHEMICAL COMPANY (US) 1987-11-03 US disclosed
WO-1987002682-A1 SEMI-PERMEABLE MEMBRANES PREPARED VIA REACTION OF CATIONIC GROUPS WITH NUCLEOPHILIC GROUPS THE DOW CHEMICAL COMPANY (US) 1987-05-07 WO disclosed
EP-0220660-A2 Semi-permeables membranes prepared via reaction of cationic groups with nucleophilic groups THE DOW CHEMICAL COMPANY (US) 1987-05-06 EP 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-10927076-B2 HSP90B N-terminal isoform-selective inhibitors HSP90AB1, HSP90AB2P, HSP90B1 ALDH1A1 1671/4885TSHR 4294/4885TDP1 1855/4885

“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.