SCHEMBL232698

SCHEMBL232698

NCC(=O)NC(Cc1ccccc1)C(=O)O

nearest known ligand 0.68

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CTSC P53634 2/20 0.60
ITGB3 P05106 2/20 0.60
ITGA2B P08514 2/20 0.60
LMNA P02545 1/20 0.59
MME P08473 1/20 0.59
ACE P12821 5/20 0.58
NPSR1 Q6W5P4 1/20 0.58
NAALAD2 Q9Y3Q0 1/20 0.56
ECE1 P42892 1/20 0.56
MMP2 P08253 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.55

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
SCHEMBL232699 1.00 CTSC (0.60) CTSCITGB3ITGA2BLMNAMME
SCHEMBL4432590 1.00 CTSC (0.60) CTSCITGB3ITGA2BLMNAMME
Water SCHEMBL28030234 0.98 CTSC (0.63) CTSCITGB3ITGA2BLMNAMME
Water SCHEMBL28030233 0.98 CTSC (0.63) CTSCITGB3ITGA2BLMNAMME
Hydrochloric Acid SCHEMBL9501928 0.98 CTSC (0.59) CTSCITGB3ITGA2BLMNAMME
Hydrochloric Acid SCHEMBL3634876 0.98 CTSC (0.59) CTSCITGB3ITGA2BLMNAMME
Bromide SCHEMBL11242978 0.98 CTSC (0.59) CTSCITGB3ITGA2BLMNAMME
Bromide SCHEMBL11242976 0.98 CTSC (0.59) CTSCITGB3ITGA2BLMNAMME
SCHEMBL8068326 0.94 MME (0.61) CTSCITGB3ITGA2BLMNAMME
SCHEMBL8068319 0.94 MME (0.61) CTSCITGB3ITGA2BLMNAMME

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12534510-B2 Peptide-receptive MHC-I complex compositions and methods THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2026-01-27 US claimed
EP-3817757-B1 PEPTIDE DEFICIENT-MHC CLASS I/CHAPERONE COMPOSITIONS AND METHODS UNIV CALIFORNIA (US) 2026-01-07 EP claimed
EP-4136098-B1 PEPTIDE-RECEPTIVE MHC-I COMPLEX COMPOSITIONS AND METHODS FOR THEIR GENERATION UNIV CALIFORNIA (US) 2025-12-17 EP claimed
US-20250027938-A1 METABOLIC SIGNATURE FOR PREDICTION OF MUCOSAL INFLAMMATION AND MICROBIAL COMPOSITION IMPERIAL COLLEGE INNOVATIONS LIMITED (GB) 2025-01-23 US claimed
CN-118703593-A Argininase quantitative detection kit, argininase qualitative detection kit and use method thereof 武汉简为医疗科技有限公司 2024-09-27 CN claimed
US-20240294601-A1 PEPTIDE DEFICIENT-MHC CLASS I/CHAPERONE COMPOSITIONS AND METHODS THE REGENTS OF THE UNIVERSITY OF CALIFORNA 2024-09-05 US claimed
CN-118384255-A Application of walnut peptide in preparation of obesity improving medicine 云南中医药大学 2024-07-26 CN claimed
EP-4370919-A1 METABOLIC SIGNATURE FOR PREDICTION OF MUCOSAL INFLAMMATION AND MICROBIAL COMPOSITION Imperial College Innovations Limited (GB) 2024-05-22 EP claimed
CN-117269494-A A group of metabolic markers for breast cancer lung metastasis 厦门大学 2023-12-22 CN claimed
US-11814420-B2 Peptide deficient-MHC class I/chaperone compositions and methods THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2023-11-14 US claimed
US-5430133-A Semi-synthetic glycosaminoglycans with heparin or heparan structure of α-L-iduronic-2-O-sulfate acid modified in position 2 ALFA WASSERMANN S.P.A. (IT) 1995-07-04 US claimed
US-5410039-A Process for the synthesis of glycosaminoglycans containing α-L-galacturonic acid substituted with nucleophilic groups in position 3 ALFA WASSERMANN S.P.A. (IT) 1995-04-25 US claimed
US-5405949-A Process for the synthesis of glycosaminoglycans with heparin or heparan structure modified in position 2 of the α-L-iduronic-2-O-sulfate acid ALFA WASSERNANN S.P.A. (IT) 1995-04-11 US claimed
EP-0618235-A1 Process for the synthesis of semisynthetic glycosaminoglycans containig alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN S.p.A. (IT) 1994-10-05 EP claimed
EP-0618234-A1 Process for the synthesis of semisynthetic glycosaminoglycans with heparin or heparan structure modified in position 2 of the alpha-L-iduronic-2-0-sulfate acid ALFA WASSERMANN S.p.A. (IT) 1994-10-05 EP claimed
EP-0565862-A2 Semi-synthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP claimed
EP-0565863-A2 Semi-synthetic glycosaminoglycans with heparin or heparan structure of alpha-L-iduronic-2-0-sulfate acid modified in position 2 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP claimed
EP-0226304-B1 COMPOSITION CONTAINING A PENEM OR CARBAPENEM ANTIBIOTIC SANKYO COMPANY LIMITED (JP) 1991-08-28 EP claimed
US-4757066-A Reduces renal toxicity SANKYO COMPANY LIMITED (JP) 1988-07-12 US claimed
EP-0226304-A1 Composition containing a penem or carbapenem antibiotic SANKYO COMPANY LIMITED (JP) 1987-06-24 EP 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 (1 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-12534510-B2 Peptide-receptive MHC-I complex compositions and methods MICA, TAP2, TAP1 CTSC 818/4885ITGB3 1089/4885ITGA2B 443/4885

“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.