SCHEMBL6732284

SCHEMBL6732284

CCOC(=O)C(C(C)=O)=C(N)C(F)(F)F

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GLO1 Q04760 1/20 0.41
ALOX15 P16050 1/20 0.40
ALDH1A1 P00352 5/20 0.37
LMNA P02545 1/20 0.37
HSD17B10 Q99714 1/20 0.37
CYP1A2 P05177 1/20 0.36
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36
MAPT P10636 2/20 0.34
CES2 O00748 3/20 0.34
ACHE P22303 3/20 0.34
CES1 P23141 3/20 0.34
NPSR1 Q6W5P4 1/20 0.33
HTT P42858 1/20 0.33
HPGD P15428 1/20 0.33
HDAC4 P56524 2/20 0.33
HDAC6 Q9UBN7 2/20 0.33
HDAC3 O15379 1/20 0.33
HDAC1 Q13547 1/20 0.33
TSHR P16473 1/20 0.32

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
SCHEMBL6732281 1.00 GLO1 (0.41) GLO1ALOX15ALDH1A1LMNAHSD17B10
SCHEMBL10820989 0.86 GLO1 (0.39) GLO1ALOX15ALDH1A1LMNAHSD17B10
SCHEMBL10820990 0.86 GLO1 (0.39) GLO1ALOX15ALDH1A1LMNAHSD17B10
SCHEMBL10364778 0.84 ALOX15 (0.39) GLO1ALOX15ALDH1A1CYP1A2MEN1
SCHEMBL10364776 0.84 ALOX15 (0.39) GLO1ALOX15ALDH1A1CYP1A2MEN1
SCHEMBL10820971 0.81 GLO1 (0.41) GLO1ALOX15ALDH1A1LMNAHSD17B10
SCHEMBL18456945 0.81 GLO1 (0.41) GLO1ALOX15ALDH1A1LMNAHSD17B10
SCHEMBL10820970 0.81 GLO1 (0.41) GLO1ALOX15ALDH1A1LMNAHSD17B10
SCHEMBL9653470 0.81 ALOX15 (0.43) GLO1ALOX15ALDH1A1LMNAHSD17B10
SCHEMBL3158392 0.81 ALOX15 (0.43) GLO1ALOX15ALDH1A1LMNAHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014126580-A1 PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO DOW AGROSCIENCES LLC (US) 2014-08-21 WO disclosed
WO-2013106254-A1 PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO DOW AGROSCIENCES LLC (US) 2013-07-18 WO disclosed
US-20040220231-A1 Substituted pyridines useful for inhibiting cholesteryl ester transfer protein activity LEE LEN F (US) 2004-11-04 US disclosed
US-6794396-B2 Substituted pyridines useful for inhibiting cholesteryl ester transfer protein activity PHARMACIA CORPORATION 2004-09-21 US disclosed
US-20040038939-A1 Substituted pyridines useful for inhibiting cholesteryl ester transfer protein activity PHARMACIA CORPORATION 2004-02-26 US disclosed
US-6605624-B1 Preventing and/or treating atherosclerosis and other coronary artery diseases PHARMACIA CORPORATION 2003-08-12 US disclosed
US-5196045-A Substituted pyridine herbicides MONSANTO COMPANY (US) 1993-03-23 US disclosed
EP-0252055-B1 SUBSTITUTED PYRIDINE HERBICIDES Monsanto Company (US) 1992-01-22 EP disclosed
US-5019153-A Substituted pyridine herbicides MONSANTO COMPANY (US) 1991-05-28 US disclosed
EP-0181852-B1 SUBSTITUTED 2,6-SUBSTITUTED PYRIDINE COMPOUNDS Monsanto Company (US) 1990-08-29 EP disclosed
EP-0182769-B1 2,6-SUBSTITUTED PYRIDINE COMPOUNDS Monsanto Company (US) 1990-08-01 EP disclosed
US-4921530-A Certain 3,5-pyridine dicarboxylates, their thio analogues having herbicidal activity MONSANTO COMPANY (US) 1990-05-01 US disclosed
US-4885026-A FLUORINE-CONTAINING METHYL GROUP AT THE 2- OR 6-POSITION; PRE- AND POSTEMERGENT MONSANTO COMPANY (US) 1989-12-05 US disclosed
US-4835279-A 2,6-substituted pyridine compounds MONSANTO COMPANY (US) 1989-05-30 US disclosed
US-4797149-A HERBICIDES MONSANTO COMPANY (US) 1989-01-10 US disclosed
EP-0252055-A1 Substituted pyridine herbicides Monsanto Company (US) 1988-01-07 EP disclosed
US-4698093-A POST, PRE EMERGENTS MONSANTO COMPANY (US) 1987-10-06 US disclosed
US-4655816-A PLANT GROWTH REGULATORS MONSANTO COMPANY (US) 1987-04-07 US disclosed
EP-0182769-A1 2,6-Substituted pyridine compounds Monsanto Company (US) 1986-05-28 EP disclosed
EP-0181852-A1 Substituted 2,6-substituted pyridine compounds Monsanto Company (US) 1986-05-21 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 (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-20040038939-A1 Substituted pyridines useful for inhibiting cholesteryl ester transfer protein activity CETP, CES1, MTTP GLO1 1210/4885ALOX15 3178/4885ALDH1A1 1154/4885
US-20040220231-A1 Substituted pyridines useful for inhibiting cholesteryl ester transfer protein activity CETP, MTTP, LCAT GLO1 1324/4885ALOX15 3254/4885ALDH1A1 1364/4885

“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.