SCHEMBL6350238

SCHEMBL6350238

C=CCOC(=O)C1CCCC1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.44
GAA P10253 1/20 0.44
KMT2A Q03164 2/20 0.39
ADRB2 P07550 1/20 0.39
ADRB1 P08588 1/20 0.39
ADRB3 P13945 1/20 0.39
CASP1 P29466 1/20 0.37
CYP3A4 P08684 1/20 0.37
NPSR1 Q6W5P4 1/20 0.36
CES2 O00748 1/20 0.36
CES1 P23141 1/20 0.36
TSHR P16473 3/20 0.36
MAPT P10636 2/20 0.36
MDM2 Q00987 1/20 0.36
NPC1 O15118 1/20 0.36
RAB9A P51151 1/20 0.36
HTT P42858 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
CACNA1B Q00975 1/20 0.35

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
SCHEMBL15443392 0.98 ALDH1A1 (0.46) ALDH1A1GAAKMT2AADRB2ADRB1
SCHEMBL15443027 0.98 ALDH1A1 (0.46) ALDH1A1GAAKMT2AADRB2ADRB1
SCHEMBL634058 0.98 ALDH1A1 (0.46) ALDH1A1GAAKMT2AADRB2ADRB1
SCHEMBL15442983 0.98 ALDH1A1 (0.46) ALDH1A1GAAKMT2AADRB2ADRB1
SCHEMBL7133197 0.96 ALDH1A1 (0.41) ALDH1A1GAAKMT2AADRB2ADRB1
SCHEMBL423892 0.91 KMT2A (0.47) ALDH1A1GAAKMT2ACASP1CYP3A4
SCHEMBL719931 0.91
SCHEMBL1218797 0.88 ALDH1A1 (0.39) ALDH1A1GAAKMT2ACASP1CYP3A4
SCHEMBL1219520 0.84 KMT2A (0.41) ALDH1A1GAAKMT2ACASP1CYP3A4
SCHEMBL11769670 0.84 KMT2A (0.41) ALDH1A1GAAKMT2ACASP1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107759483-B Preparation method of methylamino-substituted alkyl cyclopentanecarboxylate 浙江瑞博制药有限公司 2022-03-11 CN claimed
US-11779015-B2 Pesticide compositions FUNDACIÓ CENTRE DE REGULACIÓ GENÓMICA (ES) 2023-10-10 US disclosed
CN-110128288-B Preparation method of amino-substituted cyclopentane alkyl formate derivative 浙江九洲药业股份有限公司 2023-07-28 CN disclosed
CN-110128288-B Preparation method of amino-substituted cyclopentane alkyl formate derivative 浙江九洲药业股份有限公司 2023-07-28 CN disclosed
CN-107759483-B Preparation method of methylamino-substituted alkyl cyclopentanecarboxylate 浙江瑞博制药有限公司 2022-03-11 CN disclosed
CN-107759483-B Preparation method of methylamino-substituted alkyl cyclopentanecarboxylate 浙江瑞博制药有限公司 2022-03-11 CN disclosed
CN-107759483-B Preparation method of methylamino-substituted alkyl cyclopentanecarboxylate 浙江瑞博制药有限公司 2022-03-11 CN disclosed
US-20200359621-A1 PESTICIDE COMPOSITIONS FUNDACIÓ CENTRE DE REGULACIÓ GENÒMICA (ES) 2020-11-19 US disclosed
EP-3713415-A1 PESTICIDE COMPOSITIONS Fundació Centre de Regulació Genòmica (ES) 2020-09-30 EP disclosed
WO-2019101890-A1 PESTICIDE COMPOSITIONS FUNDACIÓ CENTRE DE REGULACIÓ GENÒMICA (ES) 2019-05-31 WO disclosed
US-20050165201-A1 Epoxidizing an alpha-halohydrin intermediate from a halide substitution-deesterification of an alpha -hydroxy ester derivative obtained by the coupling reaction of a phenol and a glycidyl ester BORIACK CLINTON J (US) 2005-07-28 US disclosed
US-20030149219-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom BORIACK CLINTON J (US) 2003-08-07 US disclosed
US-6534621-B2 Epoxidizing an alpha-halohydrin intermediate produced from an in situ halide substitution-deesterification of an alpha-hydroxy ester derivative DOW GLOBAL TECHNOLOGIES INC. 2003-03-18 US disclosed
EP-1290058-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC. (US) 2003-03-12 EP disclosed
US-20020045707-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom DOW GLOBAL TECHNOLOGIES INC. 2002-04-18 US disclosed
WO-2001088013-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC (US) 2001-11-22 WO disclosed
EP-0126506-A3 PREPARATION OF THE ALKYL CYCLOPENTANE-CARBOXYLATES USEFUL AS INTERMEDIATES FOR PREPARING PROSTAGLANDINS CONSIGLIO NAZIONALE DELLE RICERCHE (IT) 1985-07-31 EP disclosed
EP-0126506-A2 Preparation of the alkyl cyclopentane-carboxylates useful as intermediates for preparing prostaglandins CONSIGLIO NAZIONALE DELLE RICERCHE (IT) 1984-11-28 EP disclosed
EP-0126506-A2 Preparation of the alkyl cyclopentane-carboxylates useful as intermediates for preparing prostaglandins CONSIGLIO NAZIONALE DELLE RICERCHE (IT) 1984-11-28 EP disclosed
US-4140554-A Water-rinsable soldering fluid containing a polyamide dispersant CHEVRON RESEARCH COMPANY (US) 1979-02-20 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 (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-20200359621-A1 PESTICIDE COMPOSITIONS ADH1C, DDT, AKR1C3 ALDH1A1 35/4885GAA 3742/4885KMT2A 2852/4885
US-11779015-B2 Pesticide compositions ADH1C, DDT, AKR1C3 ALDH1A1 35/4885GAA 3742/4885KMT2A 2852/4885

“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.