SCHEMBL598263

SCHEMBL598263

CC(C)(C)OC(=O)NC(C=O)Cc1ccc(-c2ccccc2)cc1

nearest known ligand 0.61

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CTSK P43235 9/20 0.61
CTSS P25774 6/20 0.61
ATM Q13315 1/20 0.54
CTSB P07858 2/20 0.52
CTSL P07711 1/20 0.52
BCL2 P10415 1/20 0.51
ACE P12821 2/20 0.50
PPARA Q07869 2/20 0.48
PPARG P37231 1/20 0.48
MME P08473 1/20 0.48
ACE2 Q9BYF1 1/20 0.48
PTPN1 P18031 1/20 0.47
KLK5 Q9Y337 1/20 0.47

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
SCHEMBL9929938 1.00 CTSK (0.61) CTSKCTSSATMCTSBCTSL
SCHEMBL8523201 1.00 CTSK (0.61) CTSKCTSSATMCTSBCTSL
SCHEMBL7094 0.92 ATM (0.62) CTSKCTSSATMCTSBCTSL
SCHEMBL1094506 0.92 ATM (0.62) CTSKCTSSATMCTSBCTSL
SCHEMBL390555 0.92 ATM (0.62) CTSKCTSSATMCTSBCTSL
SCHEMBL16945132 0.89 CTSS (0.60) CTSKCTSSATMCTSBCTSL
SCHEMBL18995190 0.88 CTSK (0.54) CTSKCTSSATMCTSBCTSL
SCHEMBL14274169 0.88 PPARG (0.58) CTSKCTSSATMCTSBCTSL
SCHEMBL1912623 0.87 CTSL (0.50) CTSKCTSSCTSBCTSLACE
SCHEMBL30867 0.85 CTSS (0.59) CTSKCTSSATMCTSBCTSL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11370739-B2 Sacubitril intermediate and preparation method thereof SUNSHINE LAKE PHARMA CO., LTD. (CN) 2022-06-28 US disclosed
CN-112661671-B Preparation method of Sacubitril intermediate 江苏阿尔法药业股份有限公司 2022-04-22 CN disclosed
CN-112661671-A Preparation method of Sacubitril intermediate 江苏阿尔法药业有限公司 2021-04-16 CN disclosed
US-10479753-B2 Sacubitril intermediate and preparation method thereof SUNSHINE LAKE PHARMA CO., LTD (CN) 2019-11-19 US disclosed
US-20170114006-A1 SUBSTITUTED BIARYL ALKYL AMIDES BIOTHERYX, INC. 2017-04-27 US disclosed
US-9546131-B2 Substituted biaryl alkyl amides BIOTHERYX, INC. (US) 2017-01-17 US disclosed
EP-2121578-B1 PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID NOVARTIS AG (CH) 2016-08-10 EP disclosed
EP-2121578-B1 PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID NOVARTIS AG (CH) 2016-08-10 EP disclosed
US-9206116-B2 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS AG (CH) 2015-12-08 US disclosed
US-9206116-B2 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS AG (CH) 2015-12-08 US disclosed
US-20120142916-A1 PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID NOVARTIS AG (CH) 2012-06-07 US disclosed
US-8115016-B2 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS AG (CH) 2012-02-14 US disclosed
US-8115016-B2 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS AG (CH) 2012-02-14 US disclosed
US-20100113801-A1 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS PHARMACEUTICALS CORPORATION 2010-05-06 US disclosed
US-20100113801-A1 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS PHARMACEUTICALS CORPORATION 2010-05-06 US disclosed
US-20090326066-A1 PROCESS FOR PREPARING BIARYL SUBSTITUTED 4-AMINO-BUTYRIC ACID OR DERIVATIVES THEREOF AND THEIR USE IN THE PRODUCTION OF NEP INHIBITORS NOVARTIS AG (CH) 2009-12-31 US disclosed
US-20090326066-A1 PROCESS FOR PREPARING BIARYL SUBSTITUTED 4-AMINO-BUTYRIC ACID OR DERIVATIVES THEREOF AND THEIR USE IN THE PRODUCTION OF NEP INHIBITORS NOVARTIS AG (CH) 2009-12-31 US disclosed
EP-2121578-A2 NEW PROCESS Novartis AG (CH) 2009-11-25 EP disclosed
WO-2008083967-A2 PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID NOVARTIS AG (CH) 2008-07-17 WO disclosed
WO-2008083967-A2 PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID NOVARTIS AG (CH) 2008-07-17 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 (6 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-20100113801-A1 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid MME, REN, PAH CTSK 2667/4885CTSS 950/4885ATM 4839/4885
US-20120142916-A1 PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID MME, REN, PAH CTSK 2667/4885CTSS 950/4885ATM 4839/4885
US-20170114006-A1 SUBSTITUTED BIARYL ALKYL AMIDES AADAC, NAT1, GLS2 CTSK 1842/4885CTSS 879/4885ATM 2724/4885
US-20090326066-A1 PROCESS FOR PREPARING BIARYL SUBSTITUTED 4-AMINO-BUTYRIC ACID OR DERIVATIVES THEREOF AND THEIR USE IN THE PRODUCTION OF NEP INHIBITORS MME, REN, BCAT2 CTSK 2982/4885CTSS 1291/4885ATM 4871/4885
US-11370739-B2 Sacubitril intermediate and preparation method thereof DPP4, ACE, DPP8 CTSK 146/4885CTSS 378/4885ATM 3110/4885
US-10479753-B2 Sacubitril intermediate and preparation method thereof ACE, DPP4, SI CTSK 225/4885CTSS 509/4885ATM 2245/4885

“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.