SCHEMBL2556609

SCHEMBL2556609

O=CCC(=O)c1ccccc1O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 7/20 0.50
HPGD P15428 6/20 0.50
SMN1; SMN2 Q16637 4/20 0.50
ALDH1A1 P00352 3/20 0.50
CA12 O43570 1/20 0.50
CA1 P00915 1/20 0.50
CA2 P00918 1/20 0.50
HMGB1 P09429 1/20 0.50
CA4 P22748 1/20 0.50
CA6 P23280 1/20 0.50
CA7 P43166 1/20 0.50
CA9 Q16790 1/20 0.50
NAPRT Q6XQN6 1/20 0.50
CA14 Q9ULX7 1/20 0.50
MAPT P10636 6/20 0.49
MEN1 O00255 3/20 0.49
KMT2A Q03164 3/20 0.49
RAB9A P51151 1/20 0.49
KCNH2 Q12809 1/20 0.49
CYP19A1 P11511 1/20 0.49

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
SCHEMBL30730520 1.00 KDM4E (0.50) KDM4EHPGDSMN1; SMN2ALDH1A1CA12
SCHEMBL27448122 0.82 KDM4E (0.48) KDM4EHPGDSMN1; SMN2ALDH1A1CA12
SCHEMBL3803604 0.82 KDM4E (0.48) KDM4EHPGDSMN1; SMN2ALDH1A1CA12
SCHEMBL105808 0.78 KDM4E (0.58) KDM4EHPGDSMN1; SMN2ALDH1A1CA12
SCHEMBL598345 0.78 MEN1 (0.69) KDM4EHPGDSMN1; SMN2ALDH1A1CA12
SCHEMBL31211720 0.78 CYP19A1 (0.66) KDM4EHPGDSMN1; SMN2ALDH1A1CA12
SCHEMBL1125330 0.78 ALDH1A1 (0.47) KDM4EHPGDSMN1; SMN2ALDH1A1MAPT
SCHEMBL1125249 0.78 ERCC5 (0.55) KDM4EHPGDSMN1; SMN2ALDH1A1MAPT
SCHEMBL767241 0.78 ERCC5 (0.55) HPGDMEN1KMT2ARAB9ANPC1
SCHEMBL1125179 0.78 PTPN1 (0.55) HPGDALDH1A1MAPTMEN1KMT2A

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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090028751-A1 ANTI-MICROBIAL TIME CARD ROBBINS GLENN 2009-01-29 US claimed
US-6995203-B2 Flame retardant polymer compositions THE BOEING COMPANY (US) 2006-02-07 US claimed
US-20240336868-A1 COMPOSITIONS COMPRISING ADAMANTYL ESTER-CONTAINING COMPOUNDS THE PROCTER & GAMBLE COMPANY 2024-10-10 US disclosed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
US-11225655-B2 Bi-functional complexes and methods for making and using such complexes NUEVOLUTION A/S (DK) 2022-01-18 US disclosed
CN-107141299-B Substituted pyrrole chromone compound and application thereof 中山大学 2020-03-13 CN disclosed
EP-3540059-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES Nuevolution A/S (DK) 2019-09-18 EP disclosed
EP-2558577-B1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION AS (DK) 2018-12-12 EP disclosed
CN-105777725-B The application of 3- (2- furyls) chromogen ketone compounds and preparation method thereof and plant epiphyte resisting 陕西师范大学 2018-10-26 CN disclosed
CN-107141299-A A kind of substituted azole chromogen ketone compounds and its application 中山大学 2017-09-08 CN disclosed
CN-105777725-A 3-(2-furyl) chromone compound, preparation method thereof and application in resisting plant fungi 陕西师范大学 2016-07-20 CN disclosed
US-20020128522-A1 Process for the preparation of 4,4' -dihalogen-o-hydroxydiphenyl compounds TEODORO ARMANDO DI (DE) 2002-09-12 US disclosed
US-6346260-B1 HETEROCYCLIC ALKYLENEDIONE PHENOLS AND ALKYLENEDIONE PHENYL PHENOL CIBA SPECIALTY CHEMICALS CORPORATION 2002-02-12 US disclosed
US-6346260-B1 HETEROCYCLIC ALKYLENEDIONE PHENOLS AND ALKYLENEDIONE PHENYL PHENOL CIBA SPECIALTY CHEMICALS CORPORATION 2002-02-12 US disclosed
CN-1321142-A Process for preparation of 4,4'-dihalo-o-hydroxydiphenyl compounds CIBA SPECIALTY CHEMICLAS HOLDI (CH) 2001-11-07 CN disclosed
EP-1119540-A1 PROCESS FOR THE PREPARATION OF 4,4'-DIHALOGEN-O-HYDROXYDIPHENYL COMPOUNDS Ciba SC Holding AG (CH) 2001-08-01 EP disclosed
EP-1074179-A3 Microbicidal active ingredients Ciba SC Holding AG (CH) 2001-04-11 EP disclosed
EP-1074179-A2 Microbicidal active ingredients Ciba SC Holding AG (CH) 2001-02-07 EP disclosed
EP-1074179-A2 Microbicidal active ingredients Ciba SC Holding AG (CH) 2001-02-07 EP disclosed
WO-2000020366-A1 PROCESS FOR THE PREPARATION OF 4,4'-DIHALOGEN-O-HYDROXYDIPHENYL COMPOUNDS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2000-04-13 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-20020128522-A1 Process for the preparation of 4,4' -dihalogen-o-hydroxydiphenyl compounds DDT, CYP2F1, CYP4X1 KDM4E 797/4885HPGD 861/4885SMN1; SMN2 4637/4885

“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.