SCHEMBL3265463

SCHEMBL3265463

CCC(CC(N)=O)Nc1ccc(C(F)(F)F)cc1

nearest known ligand 0.45

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
KIF11 P52732 3/20 0.45
CA12 O43570 1/20 0.45
CA1 P00915 1/20 0.45
MMP2 P08253 1/20 0.45
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
HDAC1 Q13547 1/20 0.44
EPHX2 P34913 1/20 0.44
LMNA P02545 1/20 0.41
HTT P42858 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
PTGS1 P23219 2/20 0.40
LGMN Q99538 1/20 0.40
TRPV1 Q8NER1 1/20 0.40
FPR2 P25090 1/20 0.39
DHODH Q02127 1/20 0.39

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
SCHEMBL1937094 1.00 KIF11 (0.45) KIF11CA12CA1MMP2MEN1
SCHEMBL8996214 1.00 KIF11 (0.45) KIF11CA12CA1MMP2MEN1
SCHEMBL1734544 0.87 CA12 (0.46) CA12CA1MMP2MEN1KMT2A
SCHEMBL1734546 0.87 CA12 (0.46) CA12CA1MMP2MEN1KMT2A
SCHEMBL14509044 0.87 CA12 (0.46) KIF11CA12CA1MMP2MEN1
SCHEMBL8996266 0.86 FPR2 (0.45) KIF11CA12CA1MMP2MEN1
SCHEMBL1734536 0.86 HDAC1 (0.50) KIF11CA12CA1MMP2MEN1
SCHEMBL9001619 0.86 FPR2 (0.45) KIF11CA12CA1MMP2MEN1
SCHEMBL1734540 0.86 HDAC1 (0.50) KIF11CA12CA1MMP2MEN1
SCHEMBL3264266 0.84 CA12 (0.44) KIF11CA12CA1MMP2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119118998-A Preparation method of CETP inhibitor Obicetrapib (AMG-899) 上海相辉医药科技有限公司 2024-12-13 CN claimed
EP-1604975-A1 PROCESSES FOR PRODUCTION OF (R)-3- 4-(TRIFLUOROMETHYL)- PHEN YLAMINO PENTANAMIDE DERIVATIVES KANEKA CORPORATION (JP) 2005-12-14 EP claimed
US-20040199005-A1 Method for producing (R) -3- [4- (trifluoromethyl) phenylamino] -pentanoic acid amide derivative KANEKA CORPORATION (JP) 2004-10-07 US claimed
CN-119118998-A Preparation method of CETP inhibitor Obicetrapib (AMG-899) 上海相辉医药科技有限公司 2024-12-13 CN disclosed
CN-119118998-A Preparation method of CETP inhibitor Obicetrapib (AMG-899) 上海相辉医药科技有限公司 2024-12-13 CN disclosed
EP-1594843-B1 METHOD FOR PRODUCING AN OPTICALLY ACTIVE beta-amino acid derivative TAKASAGO PERFUMERY CO LTD (JP) 2013-05-22 EP disclosed
US-8188307-B2 Method for producing an optically active tetrahydroquinoline TAKASAGO INTERNATIONAL CORPORATION (JP) 2012-05-29 US disclosed
US-20100036149-A1 METHOD FOR PRODUCING AN OPTICALLY ACTIVE TETRAHYDROQUINOLINE TAKASAGO INTERNATIONAL COPORATION (JP) 2010-02-11 US disclosed
US-7601842-B2 Method for producing an optically active tetrahydroquinoline TAKASAGO INTERNATIONAL CORPORATION (JP) 2009-10-13 US disclosed
CN-1972927-A Compounds and methods for treating dyslipidemia LILLY CO ELI (US) 2007-05-30 CN disclosed
US-7223859-B2 Method for producing (R)-3-[4-(trifluoromethyl) phenylamino]-pentanoic acid amide derivative PFIZER INC. (US) 2007-05-29 US disclosed
US-20040199005-A1 Method for producing (R) -3- [4- (trifluoromethyl) phenylamino] -pentanoic acid amide derivative KANEKA CORPORATION (JP) 2004-10-07 US disclosed
US-20040199005-A1 Method for producing (R) -3- [4- (trifluoromethyl) phenylamino] -pentanoic acid amide derivative KANEKA CORPORATION (JP) 2004-10-07 US disclosed
WO-2004083166-A1 PROCESSES FOR PRODUCTION OF (R)-3-[4-(TRIFLUOROMETHYL)- PHENYLAMINO]PENTANAMIDE DERIVATIVES KANEKA CORPORATION (JP) 2004-09-30 WO disclosed
WO-2004074255-A2 METHOD FOR PRODUCING AN OPTICALLY ACTIVE TETRAHYDROQUINOLINE TAKASAGO INTERNATIONAL CORPORATION (JP) 2004-09-02 WO disclosed
EP-1425270-A2 METHODS AND INTERMEDIATES FOR PREPARING 4-AMINOQUINOLINE CETP INHIBITORS Pfizer Products Inc. (US) 2004-06-09 EP disclosed
EP-1383734-A2 COMPOUNDS USEFUL AS INTERMEDIATES FOR 4-AMINOQUINOLINE DERIVATIVES Pfizer Products Inc. (US) 2004-01-28 EP disclosed
WO-2002088069-A9 COMPOUNDS USEFUL AS INTERMEDIATES FOR 4-AMINOQUINOLINE DERIVATIVES PFIZER PROD INC (US) 2003-12-04 WO disclosed
WO-2002088085-A2 METHODS AND INTERMEDIATES FOR PREPARING 4-AMINOQUINOLINE CETP INHIBITORS PFIZER PRODUCTS INC. (US) 2002-11-07 WO disclosed
WO-2002088069-A2 COMPOUNDS USEFUL AS INTERMEDIATES FOR 4-AMINOQUINOLINE DERIVATIVES PFIZER PRODUCTS INC. (US) 2002-11-07 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 (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-20100036149-A1 METHOD FOR PRODUCING AN OPTICALLY ACTIVE TETRAHYDROQUINOLINE AADAT, KMO, ALDH7A1 KIF11 2810/4885CA12 2615/4885CA1 1662/4885
US-20040199005-A1 Method for producing (R) -3- [4- (trifluoromethyl) phenylamino] -pentanoic acid amide derivative CETP, PCTP, MTTP KIF11 3837/4885CA12 3484/4885CA1 2155/4885

“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.