SCHEMBL7326080

SCHEMBL7326080

C[C@H](N)C(=O)Oc1ccccc1I

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FABP7 O15540 1/20 0.42
▸ FABP3 P05413 1/20 0.42
▸ FABP5 Q01469 1/20 0.42
▸ IRAK4 Q9NWZ3 1/20 0.39
▸ ALDH1A1 P00352 4/20 0.37
▸ ACHE P22303 1/20 0.37
▸ XIAP P98170 1/20 0.35
▸ KDM4E B2RXH2 3/20 0.35
▸ HPGD P15428 2/20 0.35
▸ HSD17B10 Q99714 2/20 0.35
▸ KMT2A Q03164 2/20 0.35
▸ HTT P42858 1/20 0.34
▸ GAA P10253 1/20 0.34
▸ BCHE P06276 1/20 0.34
▸ TSHR P16473 2/20 0.33
▸ LMNA P02545 1/20 0.33
▸ CYP1A2 P05177 1/20 0.33
▸ CARM1 Q86X55 1/20 0.33
▸ PRMT6 Q96LA8 1/20 0.33
▸ TAAR1 Q96RJ0 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
SCHEMBL27996039 0.85 ELANE (0.46) FABP7FABP3FABP5IRAK4ALDH1A1
SCHEMBL23867037 0.84 FABP7 (0.43) FABP7FABP3FABP5IRAK4ALDH1A1
SCHEMBL1983875 0.80 TSHR (0.46) IRAK4ALDH1A1ACHEXIAPKDM4E
SCHEMBL3199566 0.80 KMT2A (0.51) IRAK4ALDH1A1KDM4EKMT2AHTT
SCHEMBL5062924 0.80 TDP1 (0.46) IRAK4ALDH1A1KDM4EHPGDKMT2A
SCHEMBL5058437 0.80 TDP1 (0.46) IRAK4ALDH1A1KDM4EHPGDKMT2A
SCHEMBL8399530 0.80 CA1 (0.45) IRAK4ALDH1A1ACHEKDM4EHPGD
SCHEMBL7976424 0.80 KMT2A (0.51) IRAK4ALDH1A1KDM4EKMT2AHTT
SCHEMBL28842455 0.80 TSHR (0.46) IRAK4ALDH1A1ACHEXIAPKDM4E
SCHEMBL27620015 0.79 FABP7 (0.45) FABP7FABP3FABP5IRAK4ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260014282-A1 METHODS OF FORMING RADIOPAQUE PEPTIDES FOR USE IN MEDICAL HYDROGELS BOSTON SCIENTIFIC SCIMED, INC. (US) 2026-01-15 — — US 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
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
US-20260014282-A1 METHODS OF FORMING RADIOPAQUE PEPTIDES FOR USE IN MEDICAL HYDROGELS BOSTON SCIENTIFIC SCIMED, INC. (US) 2026-01-15 — — US disclosed
CN-105026574-B Cell lines 米迪缪尼有限公司 2019-08-30 — — CN disclosed
CN-103917538-B 2-(1,2,3-triazole-2-base) Benzoylamide and 3-(1,2,3-triazole-2-base) picolinamide derivatives 埃科特莱茵药品有限公司 2016-08-24 — — CN disclosed
EP-2776430-B1 2- (1,2,3-TRIAZOL-2-YL) BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL) PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS ACTELION PHARMACEUTICALS LTD (CH) 2016-03-16 — — EP disclosed
US-9150566-B2 2-(1,2,3-triazol-2-yl)benzamide and 3-(1,2,3-triazol-2-YL)picolinamide derivatives as orexin receptor antagonists ACTELION PHARMACEUTICALS LTD. (CH) 2015-10-06 — — US disclosed
US-20150158855-A1 2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS ACTELION PHARMACEUTICALS LTD. (CH) 2015-06-11 — — US disclosed
EP-2776430-A1 2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS Actelion Pharmaceuticals Ltd. (CH) 2014-09-17 — — EP disclosed
WO-2013068935-A1 2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS ACTELION PHARMACEUTICALS LTD (CH) 2013-05-16 — — WO disclosed
CN-1838950-A Methods for treating protein aggregation disorders NEUROCHEM INTERNAT LTD (CH) 2006-09-27 — — CN disclosed
CN-1575816-A Compounds for the treatment of female sexual dysfunction PFIZER (US) 2005-02-09 — — CN disclosed
CN-1328824-A Compounds for the treatment of female sexual dysfunction PFIZER (US) 2002-01-02 — — CN disclosed
US-6232305-B1 ANTICANCER AGENTS; BONE DISORDERS; ANTIARTHRITIC AGENTS; RESPIRATORY SYSTEM DISORDERS NAEJA PHARMACEUTICAL INC. (CA) 2001-05-15 — — US disclosed
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 disclosed
WO-1998032766-A1 SUBSTITUTED AMINO BICYCLIC-β-LACTAM PENAM AND CEPHAM DERIVATIVES AS CYSTEINE PROTEASE INHIBITORS SYNPHAR LABORATORIES INC. (US) 1998-07-30 — — 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-20150158855-A1 2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS HCRTR2, HCRTR1, NPY1R FABP7 2694/4885FABP3 4217/4885FABP5 3267/4885
US-20260014282-A1 METHODS OF FORMING RADIOPAQUE PEPTIDES FOR USE IN MEDICAL HYDROGELS IAPP, NPPA, ARG1 FABP7 1254/4885FABP3 389/4885FABP5 2328/4885

“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.

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