SCHEMBL359159

SCHEMBL359159

C[C@H](N)C(=O)Oc1ccccn1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.43
NPC1 O15118 1/20 0.43
RAB9A P51151 1/20 0.43
CYP3A4 P08684 2/20 0.41
CYP1A2 P05177 2/20 0.41
ALDH1A1 P00352 4/20 0.39
TSHR P16473 2/20 0.38
XIAP P98170 1/20 0.38
BIRC2 Q13490 1/20 0.38
KDM4E B2RXH2 2/20 0.38
LMNA P02545 2/20 0.38
ABCB11 O95342 1/20 0.38
ESR1 P03372 1/20 0.38
ADRA2A P08913 1/20 0.38
CYP2C9 P11712 1/20 0.38
PDE4A P27815 1/20 0.38
ADRA1A P35348 1/20 0.38
OPRK1 P41145 1/20 0.38
STAT6 P42226 1/20 0.38
SLC6A3 Q01959 1/20 0.38

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
SCHEMBL3718331 1.00 SMN1; SMN2 (0.43) SMN1; SMN2NPC1RAB9ACYP3A4CYP1A2
Hydrochloric Acid SCHEMBL9641232 0.98 SMN1; SMN2 (0.42) SMN1; SMN2NPC1RAB9ACYP3A4CYP1A2
SCHEMBL10985870 0.81 ALDH1A1 (0.42) SMN1; SMN2NPC1RAB9ACYP3A4CYP1A2
SCHEMBL27864513 0.80 SMN1; SMN2 (0.44) SMN1; SMN2NPC1RAB9ACYP3A4CYP1A2
SCHEMBL7511792 0.79 NPC1 (0.39) SMN1; SMN2NPC1RAB9ACYP3A4CYP1A2
SCHEMBL21137978 0.79 SLC1A5 (0.41) SMN1; SMN2NPC1RAB9ACYP1A2ALDH1A1
SCHEMBL6658582 0.79 SLC1A5 (0.41) SMN1; SMN2NPC1RAB9ACYP1A2ALDH1A1
SCHEMBL15156598 0.78 PTPRA (0.42) SMN1; SMN2NPC1RAB9ACYP1A2ALDH1A1
SCHEMBL28426909 0.77 P4HTM (0.44) SMN1; SMN2NPC1RAB9ACYP3A4CYP1A2
Methyl Alcohol SCHEMBL11294525 0.77 PTPRA (0.41) SMN1; SMN2NPC1RAB9ACYP3A4CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109988312-B Polyamide acid ester, preparation method, negative polyimide composition and application 深圳先进技术研究院 2023-04-11 CN claimed
US-20210206835-A1 Self-Assembling Collagen-Like Polypeptides for Applications and Uses Related Thereto NATIONAL SCIENCE FOUNDATION 2021-07-08 US claimed
US-20140309273-A1 COMPOUNDS AND METHODS OF TREATING OBESITY YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD. (IL) 2014-10-16 US claimed
US-20110178151-A1 COMPOUNDS AND METHODS OF TREATING OBESITY YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW (IL) 2011-07-21 US claimed
EP-2262763-A2 COMPOUNDS AND METHODS OF TREATING OBESITY Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. (IL) 2010-12-22 EP claimed
WO-2009109973-A2 COMPOUNDS AND METHODS OF TREATING OBESITY YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD. (IL) 2009-09-11 WO claimed
CN-101495502-A N-terminally modified GLP-1 receptor modulators BRISTOL MYERS SQUIBB CO (US) 2009-07-29 CN claimed
US-20080045461-A1 N-TERMINALLY MODIFIED GLP-1 RECEPTOR MODULATORS BRISTOL-MYERS SQUIBB COMPANY 2008-02-21 US claimed
EP-1179056-B1 MIXED-BED SOLID PHASE AND ITS USE IN THE ISOLATION OF NUCLEIC ACIDS PROMEGA CORP (US) 2004-07-28 EP claimed
JP-2002543980-A 2002-12-24 JP claimed
WO-2000070041-A1 MIXED-BED SOLID PHASE AND ITS USE IN THE ISOLATION OF NUCLEIC ACIDS PROMEGA CORPORATION (US) 2000-11-23 WO claimed
EP-0961779-A1 SUBSTITUTED AMINO BICYCLIC-$g(b)-LACTAM PENAM AND CEPHAM DERIVATIVES AS CYSTEINE PROTEASE INHIBITORS SYNPHAR LABORATORIES INC. (CA) 1999-12-08 EP claimed
EP-0950046-A1 3,4-DISUBSTITUTED AZETIDIN-2-ONE DERIVATIVES USEFUL AS CYSTEINE PROTEINASE REGULATORS SYNPHAR LABORATORIES INC. (CA) 1999-10-20 EP claimed
US-5959123-A REACATING SUBSTITUTED AMINO ACID WITH 3-AMINO-4-SUBSTITUTED-AZETIDINE-2-ONE COMPOUND TO FORM 3, 4-DISUBSTITUTED-AZETIDINE-2-ONE COMPOUND; USEFUL FOR TREATING MUSCULAR DYSTROPHY, ARTHRITIS, VIRAL AND PARASITIC INFECTIONS SYNPHAR LABORATORIES, INC. (CA) 1999-09-28 US claimed
WO-1998032766-A1 SUBSTITUTED AMINO BICYCLIC-β-LACTAM PENAM AND CEPHAM DERIVATIVES AS CYSTEINE PROTEASE INHIBITORS SYNPHAR LABORATORIES INC. (US) 1998-07-30 WO claimed
WO-1998012176-A1 3,4-DISUBSTITUTED AZETIDIN-2-ONE DERIVATIVES USEFUL AS CYSTEINE PROTEINASE REGULATORS SYNPHAR LABORATORIES INC. (US) 1998-03-26 WO claimed
WO-1997011958-A1 PROTEIN SIGNATURE ANALYSIS THE SCRIPPS RESEARCH INSTITUTE (US) 1997-04-03 WO claimed
EP-0656904-A1 PEPTIDE INHIBITORS OF SELECTIN BINDING CENTOCOR INC. (US) 1995-06-14 EP claimed
EP-0606222-A1 CYCLIC HEXAPEPTIDES AS TACHYQUININ ANTAGONISTS, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THEREOF A. MENARINI INDUSTRIE FARMACEUTICHE RIUNITE S.R.L. (IT) 1994-07-20 EP claimed
WO-1993024526-A1 PEPTIDE INHIBITORS OF SELECTIN BINDING CENTOCOR, INC. (US) 1993-12-09 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-20140309273-A1 COMPOUNDS AND METHODS OF TREATING OBESITY FABP4, LIPC, GPR119 SMN1; SMN2 2751/4885NPC1 146/4885RAB9A 2307/4885
US-20080045461-A1 N-TERMINALLY MODIFIED GLP-1 RECEPTOR MODULATORS GLP1R, GIPR, IAPP SMN1; SMN2 631/4885NPC1 3199/4885RAB9A 1569/4885
US-20110178151-A1 COMPOUNDS AND METHODS OF TREATING OBESITY GPR119, FABP4, LIPC SMN1; SMN2 3157/4885NPC1 132/4885RAB9A 2272/4885

“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.