SCHEMBL598389

SCHEMBL598389

C[C@H]1C[C@@H](Cc2ccc(-c3ccccc3)cc2)N(C(=O)OC(C)(C)C)C1=O

nearest known ligand 0.45

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
KLK7 P49862 6/20 0.45
KLK5 Q9Y337 5/20 0.42
PRSS1 P07477 2/20 0.41
PRSS2 P07478 2/20 0.41
PRSS3 P35030 2/20 0.41
USP30 Q70CQ3 3/20 0.40
NR1H2 P55055 4/20 0.39
NR1H3 Q13133 4/20 0.39
PLA2G10 O15496 1/20 0.39
PLA2G5 P39877 1/20 0.39
DPP4 P27487 1/20 0.38
STS P08842 1/20 0.38
CETP P11597 1/20 0.38
RXRA P19793 1/20 0.38
ABHD6 Q9BV23 1/20 0.38
DAGLA Q9Y4D2 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
SCHEMBL598255 1.00 KLK7 (0.45) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL1908567 1.00 KLK7 (0.45) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL3424651 1.00 KLK7 (0.45) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL17169858 0.94 KLK7 (0.50) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL29997836 0.94 KLK7 (0.50) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL19605628 0.88 KLK7 (0.45) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL18724921 0.88 KLK7 (0.45) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL19605627 0.88 KLK7 (0.45) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL9963887 0.88 KLK7 (0.45) KLK7KLK5PRSS1PRSS2PRSS3
SCHEMBL12519985 0.87 KLK7 (0.47) KLK7KLK5PRSS1PRSS2PRSS3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9802887-B2 Process for the preparation of intermediates useful for the manufacture NEP inhibitors NOVARTIS AG (CH) 2017-10-31 US disclosed
US-9403766-B2 Intermediates for producing NEP inhibitors or prodrugs thereof NOVARTIS AG (CH) 2016-08-02 US disclosed
US-20160060217-A1 Processes HOOK DAVID (CH) 2016-03-03 US disclosed
US-9227934-B2 Processes for producing NEP inhibitors or prodrugs thereof NOVARTIS AG (CH) 2016-01-05 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-20150274650-A1 PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL FOR THE MANUFACTURE NEP INHIBITORS HOOK DAVID (CH) 2015-10-01 US disclosed
US-20150246881-A1 Processes NOVARTIS AG (CH) 2015-09-03 US disclosed
US-9085529-B2 Process for the preparation of intermediates useful for the manufacture NEP inhibitors NOVARTIS AG (CH) 2015-07-21 US disclosed
US-9061973-B2 Processes for producing NEP inhibitors or prodrugs thereof NOVARTIS PHARMACEUTICALS CORPORATION (US) 2015-06-23 US disclosed
US-20150166468-A1 Process for Preparing 5-biphenyl-4-amino-2-methyl Pentanoic Acid NOVARTIS AG (CH) 2015-06-18 US disclosed
US-8993785-B2 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS AG (CH) 2015-03-31 US disclosed
US-20140249320-A1 Process for Preparing 5-biphenyl-4-amino-2-methyl Pentanoic Acid NOVARTIS AG (CH) 2014-09-04 US disclosed
US-20140243546-A1 Processes NOVARTIS AG (CH) 2014-08-28 US disclosed
US-8716495-B2 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS AG (CH) 2014-05-06 US disclosed
US-8580974-B2 Processes NOVARTIS AG (CH) 2013-11-12 US disclosed
US-20130158275-A1 NEW PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL FOR THE MANUFACTURE NEP INHIBITORS NOVARTIS AG (CH) 2013-06-20 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-20110046397-A1 NEW PROCESSES NOVARTIS PHARMACEUTICALS CORPORATION 2011-02-24 US disclosed
US-20100113801-A1 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid NOVARTIS PHARMACEUTICALS CORPORATION 2010-05-06 US 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 (10 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-20160060217-A1 Processes MME, NAT1, AGTR1 KLK7 2704/4885KLK5 1869/4885PRSS1 509/4885
US-20110046397-A1 NEW PROCESSES MME, REN, AGTR1 KLK7 2766/4885KLK5 1892/4885PRSS1 569/4885
US-20130158275-A1 NEW PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL FOR THE MANUFACTURE NEP INHIBITORS MME, DNPEP, REN KLK7 2897/4885KLK5 1766/4885PRSS1 202/4885
US-20100113801-A1 Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid MME, REN, PAH KLK7 3403/4885KLK5 1873/4885PRSS1 363/4885
US-20120142916-A1 PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID MME, REN, PAH KLK7 3403/4885KLK5 1873/4885PRSS1 363/4885
US-20140249320-A1 Process for Preparing 5-biphenyl-4-amino-2-methyl Pentanoic Acid MME, REN, PAH KLK7 3403/4885KLK5 1873/4885PRSS1 363/4885
US-20150166468-A1 Process for Preparing 5-biphenyl-4-amino-2-methyl Pentanoic Acid MME, REN, PAH KLK7 3403/4885KLK5 1873/4885PRSS1 363/4885
US-20150274650-A1 PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL FOR THE MANUFACTURE NEP INHIBITORS MME, DNPEP, REN KLK7 2446/4885KLK5 1752/4885PRSS1 364/4885
US-20140243546-A1 Processes MME, NAT1, AGTR1 KLK7 2704/4885KLK5 1869/4885PRSS1 509/4885
US-20150246881-A1 Processes MME, NAT1, AGTR1 KLK7 2704/4885KLK5 1869/4885PRSS1 509/4885

“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.