SCHEMBL2921177

SCHEMBL2921177

CC(C)=CCCC(C)=CCCC(C)=CCC(=O)O

nearest known ligand 0.69

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
FNTA P49354 5/20 0.69
FNTB P49356 5/20 0.69
KMT2A Q03164 4/20 0.64
MAPT P10636 3/20 0.61
MEN1 O00255 3/20 0.61
TRPA1 O75762 1/20 0.61
KDM4E B2RXH2 1/20 0.59
ATM Q13315 1/20 0.59
ALOX15 P16050 3/20 0.57
CYP3A4 P08684 2/20 0.57
ALDH1A1 P00352 2/20 0.57
UGT1A1 P22309 1/20 0.57
POLB P06746 1/20 0.57
SQLE Q14534 1/20 0.55

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
SCHEMBL15315193 1.00 FNTA (0.69) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL1105228 1.00 FNTA (0.69) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL11619480 1.00 FNTA (0.69) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL8758581 1.00 FNTA (0.69) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL11619483 1.00 FNTA (0.69) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL806737 0.98 FNTA (0.66) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL1409916 0.98 FNTA (0.66) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL5361163 0.98 FNTA (0.66) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL28603272 0.94 FNTA (0.63) FNTAFNTBKMT2AMAPTMEN1
SCHEMBL1395165 0.87 FNTA (0.72) FNTAFNTBKMT2AMAPTMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111741943-B Method for isomerising 3- (Z) -unsaturated carboxylic acids into 3- (E) -isomers 巴斯夫欧洲公司 2024-07-02 CN claimed
CN-114989000-B Process for preparing unsaturated carboxylic acids by carbonylation of allyl alcohol and its acylated products 巴斯夫欧洲公司 2024-05-10 CN claimed
EP-2922813-B1 HYDROCARBONYLATION OR METHOXYCARBONYLATION OF 1,3-DIENE DERIVATIVES WITH PALLADIUM COMPLEX FIRMENICH & CIE (CH) 2016-10-12 EP claimed
US-9376365-B2 Hydrocarbonylation or methoxycarbonylation of 1,3-diene derivatives with palladium complex FIRMENICH SA (CH) 2016-06-28 US claimed
US-20150299085-A1 HYDROCARBONYLATION OR METHOXYCARBONYLATION OF 1,3-DIENE DERIVATIVES WITH PALLADIUM COMPLEX FIRMENICH SA (CH) 2015-10-22 US claimed
EP-2922813-A1 HYDROCARBONYLATION OR METHOXYCARBONYLATION OF 1,3-DIENE DERIVATIVES WITH PALLADIUM COMPLEX Firmenich SA (CH) 2015-09-30 EP claimed
WO-2014079691-A1 HYDROCARBONYLATION OR METHOXYCARBONYLATION OF 1,3-DIENE DERIVATIVES WITH PALLADIUM COMPLEX FIRMENICH SA (CH) 2014-05-30 WO claimed
US-4520029-A ANTIINFLAMMATORY AND ANTIULCER AGENTS KOTOBUKI SEIYAKU CO., LTD. (JP) 1985-05-28 US claimed
JP-2258773-A None JP disclosed
JP-60123483-A None JP disclosed
US-12172956-B2 Method for the isomerization of a 3-(Z)-unsaturated carboxylic acid to the 3-(E)-isomer BASF SE (DE) 2024-12-24 US disclosed
CN-111741943-B Method for isomerising 3- (Z) -unsaturated carboxylic acids into 3- (E) -isomers 巴斯夫欧洲公司 2024-07-02 CN disclosed
CN-114989000-B Process for preparing unsaturated carboxylic acids by carbonylation of allyl alcohol and its acylated products 巴斯夫欧洲公司 2024-05-10 CN disclosed
CN-110325646-B Process for preparing (3E, 7E) -Gao Fani acid or (3E, 7E) -Gao Fani acid esters 巴斯夫欧洲公司 2024-02-09 CN disclosed
US-4520029-A ANTIINFLAMMATORY AND ANTIULCER AGENTS KOTOBUKI SEIYAKU CO., LTD. (JP) 1985-05-28 US disclosed
US-4520029-A ANTIINFLAMMATORY AND ANTIULCER AGENTS KOTOBUKI SEIYAKU CO., LTD. (JP) 1985-05-28 US disclosed
US-4503240-A Process for preparing 8,12-epoxy-13,14,15,16-tetranorlabdane Consortium F/u/ r Elektrochemische Industrie GmbH (DE) 1985-03-05 US disclosed
US-4209529-A ANTIULCER AGENTS KOTOBUKI SEIYAKU COMPANY LIMITED (JP) 1980-06-24 US disclosed
US-4209529-A ANTIULCER AGENTS KOTOBUKI SEIYAKU COMPANY LIMITED (JP) 1980-06-24 US disclosed
US-4116955-A META-CYCLOPHANE AND A TRANS-TERPENOID, SEPARATION OF ISOMERS TEIJIN LIMITED (JP) 1978-09-26 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-20150299085-A1 HYDROCARBONYLATION OR METHOXYCARBONYLATION OF 1,3-DIENE DERIVATIVES WITH PALLADIUM COMPLEX PHOSPHO1, PDCD1LG2, PDK2 FNTA 1235/4885FNTB 928/4885KMT2A 555/4885
US-12172956-B2 Method for the isomerization of a 3-(Z)-unsaturated carboxylic acid to the 3-(E)-isomer HCAR2, HCAR1, AKR1C3 FNTA 1530/4885FNTB 2615/4885KMT2A 2629/4885

“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.