SCHEMBL296159

SCHEMBL296159

CCCOC(=O)C1C(C=C(C)C)C1(C)C

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.76
CYP1A2 P05177 4/20 0.47
CYP2C19 P33261 4/20 0.47
TDP1 Q9NUW8 3/20 0.47
CYP3A4 P08684 2/20 0.47
CYP2D6 P10635 1/20 0.47
CYP2C9 P11712 1/20 0.47
TSHR P16473 4/20 0.44
ALOX15 P16050 1/20 0.38
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
TRPV1 Q8NER1 1/20 0.36
ADRA2A P08913 1/20 0.36
CNR1 P21554 1/20 0.36
ATM Q13315 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
NPSR1 Q6W5P4 1/20 0.35
PPM1B O75688 1/20 0.33
PTPN1 P18031 1/20 0.33
PPP1CC P36873 1/20 0.33

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
SCHEMBL809165 0.90 LMNA (0.71) LMNACYP1A2CYP2C19TDP1CYP3A4
SCHEMBL27601600 0.89 LMNA (0.69) LMNACYP1A2CYP2C19TDP1CYP3A4
SCHEMBL294548 0.87 LMNA (0.57) LMNACYP1A2CYP2C19TDP1CYP3A4
Chrysanthemic Acid, Ethyl Ester SCHEMBL6054986 0.86 LMNA (1.00) LMNACYP1A2CYP2C19TDP1CYP3A4
Chrysanthemic Acid, Ethyl Ester SCHEMBL10712272 0.86 LMNA (1.00) LMNACYP1A2CYP2C19TDP1CYP3A4
Chrysanthemic Acid, Ethyl Ester SCHEMBL10846022 0.86 LMNA (1.00) LMNACYP1A2CYP2C19TDP1CYP3A4
Chrysanthemic Acid, Ethyl Ester SCHEMBL3676624 0.86 LMNA (1.00) LMNACYP1A2CYP2C19TDP1CYP3A4
Chrysanthemic Acid, Ethyl Ester SCHEMBL294267 0.86 LMNA (1.00) LMNACYP1A2CYP2C19TDP1CYP3A4
Chrysanthemic Acid, Ethyl Ester SCHEMBL18231332 0.86 LMNA (1.00) LMNACYP1A2CYP2C19TDP1CYP3A4
SCHEMBL2167455 0.86 LMNA (0.56) LMNACYP1A2CYP2C19TDP1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112301065-A Preparation method of dextro-cis-first chrysanthemic acid 江苏扬农化工股份有限公司 2021-02-02 CN claimed
CN-108486170-A A kind of preparation method of d-trans dichlor chrysanthemic acid 江苏扬农化工股份有限公司 2018-09-04 CN claimed
US-4788323-A Method for racemization of optically active chrysanthemic acid or its ester SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1988-11-29 US claimed
US-4659864-A USING ALUMINUM BORMIDE AND A HYDROPEROXIDE SUMITOMO CHEMICAL COMPANY, LTD. (JP) 1987-04-21 US claimed
CN-115044922-A Preparation method of pyridino-imidazole skeleton fused ring compound under electrocatalysis 青岛科技大学 2022-09-13 CN disclosed
CN-112301065-A Preparation method of dextro-cis-first chrysanthemic acid 江苏扬农化工股份有限公司 2021-02-02 CN disclosed
CN-108486170-A A kind of preparation method of d-trans dichlor chrysanthemic acid 江苏扬农化工股份有限公司 2018-09-04 CN disclosed
EP-1792889-B1 Process for the preparation of carboxylic acid esters SUMITOMO CHEMICAL CO (JP) 2015-03-04 EP disclosed
EP-1547995-B1 Process for the preparation of carboxylic acid esters SUMITOMO CHEMICAL CO (JP) 2014-05-07 EP disclosed
EP-1683783-B1 Chiral copper complex and production processes thereof and using the same SUMITOMO CHEMICAL CO (JP) 2012-03-14 EP disclosed
EP-1683782-B1 Chiral copper complex and production processes thereof and using the same SUMITOMO CHEMICAL CO (JP) 2012-03-14 EP disclosed
US-7741511-B2 Process for the preparation of carboxylic acid esters SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-06-22 US disclosed
EP-0299760-A1 Method for racemization of optically active chrysanthemic acid or its derivatives SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1989-01-18 EP disclosed
US-4788323-A Method for racemization of optically active chrysanthemic acid or its ester SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1988-11-29 US disclosed
EP-0282221-A2 Method for racemization of optically active chrysanthemic acid or its ester SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1988-09-14 EP disclosed
EP-0261824-A1 Method for racemization of optically active chrysanthemic acid or its ester SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1988-03-30 EP disclosed
US-4723035-A Method for racemization of chrysanthemic acid or its ester SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1988-02-02 US disclosed
EP-0235940-A1 Method for racemization of chrysanthemic acid or its ester SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1987-09-09 EP disclosed
US-4659864-A USING ALUMINUM BORMIDE AND A HYDROPEROXIDE SUMITOMO CHEMICAL COMPANY, LTD. (JP) 1987-04-21 US disclosed
EP-0165070-A2 Method for racemization of chrysanthemic acid or its ester SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1985-12-18 EP disclosed