SCHEMBL901541

SCHEMBL901541

CCOC(=O)C(CCc1ccccc1)N[C@@H](CCCCNC(=O)C(F)(F)F)C(=O)O

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MME P08473 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.43
ACE P12821 7/20 0.43
POLB P06746 1/20 0.43
SIRT2 Q8IXJ6 2/20 0.42
SIRT1 Q96EB6 2/20 0.42
LMNA P02545 1/20 0.42
HDAC3 O15379 1/20 0.42
HDAC4 P56524 1/20 0.42
HDAC1 Q13547 1/20 0.42
HDAC7 Q8WUI4 1/20 0.42
HDAC2 Q92769 1/20 0.42
HDAC10 Q969S8 1/20 0.42
HDAC11 Q96DB2 1/20 0.42
HDAC8 Q9BY41 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
HDAC9 Q9UKV0 1/20 0.42
HDAC5 Q9UQL6 1/20 0.42
NCOR2 Q9Y618 1/20 0.42
FOLH1 Q04609 2/20 0.41

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
SCHEMBL15101628 1.00 MME (0.45) MMESMN1; SMN2ACEPOLBSIRT2
SCHEMBL901542 1.00 MME (0.45) MMESMN1; SMN2ACEPOLBSIRT2
SCHEMBL5346764 0.97 SMN1; SMN2 (0.46) SMN1; SMN2ACEPOLBSIRT2SIRT1
SCHEMBL21373191 0.93 MME (0.46) MMEACEPOLBSIRT2SIRT1
SCHEMBL30313716 0.93 MME (0.46) MMEACEPOLBSIRT2SIRT1
SCHEMBL14423531 0.91 MME (0.52) MMESMN1; SMN2ACEPOLBFOLH1
SCHEMBL3373746 0.91 MME (0.52) MMESMN1; SMN2ACEPOLBFOLH1
SCHEMBL30313811 0.90 MME (0.43) MMESMN1; SMN2ACEPOLBSIRT2
SCHEMBL21373190 0.90 MME (0.43) MMESMN1; SMN2ACEPOLBSIRT2
SCHEMBL14423532 0.90 SMN1; SMN2 (0.48) SMN1; SMN2ACEPOLBLMNAHDAC3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8940929-B2 Preparation method of high-optical purity N2-[1 -(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine ABA CHEMICALS CORPORATION (CN) 2015-01-27 US claimed
US-20130178651-A1 PREPARATION METHOD OF HIGH-OPTICAL PURITY N2-[1-(S)-ETHOXYCARBONYL-3-PHENYLPROPYL]-N6-TRIFLUOROACETYL-L-LYSINE ABA CHEMICALS CORPORATION (CN) 2013-07-11 US claimed
US-7253299-B2 Process for purifying n2-(1(s)-ethoxycarbonyl-3-phenylpropyl)-n6-thifluoroacetyl-l-lysine KANEKA CORPORATION (JP) 2007-08-07 US claimed
US-20040147773-A1 Process for purifying n2-(1(s)-ethoxycarbonyl -3-phenylpropyl)-n6-thifluoroacetyl-l-lysine KANEKA CORPORATION (JP) 2004-07-29 US claimed
EP-1405845-A1 METHOD FOR PURIFYING N2-(1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL)-N6-TRIFLUOROACETYL-L-LYSINE KANEKA CORPORATION (JP) 2004-04-07 EP claimed
EP-0239062-B1 N2-(1-CARBOXY-3-OXO-3-PHENYLPROPYL)-L-LYSINE COMPOUNDS AND THEIR DERIVATIVES KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1991-05-29 EP claimed
EP-0239062-A2 N2-(1-carboxy-3-oxo-3-phenylpropyl)-L-Lysine compounds and their derivatives KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-09-30 EP claimed
JP-8253497-A None JP disclosed
EP-3543225-B1 METHOD FOR PREPARING LISINOPRIL INTERMEDIATE ZHEJIANG HUAHAI PHARM CO LTD (CN) 2023-01-04 EP disclosed
CN-113698313-A Method for recovering lisinopril chiral intermediate 浙江华海药业股份有限公司 2021-11-26 CN disclosed
CN-111732627-A Synthesis method of lisinopril impurity J 浙江华海药业股份有限公司 2020-10-02 CN disclosed
US-10633329-B2 Method for preparing lisinopril intermediate ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. (CN) 2020-04-28 US disclosed
EP-3543225-A1 METHOD FOR PREPARING LISINOPRIL INTERMEDIATE Zhejiang Huahai Pharmaceutical Co., Ltd (CN) 2019-09-25 EP disclosed
EP-0903337-A1 PROCESS FOR THE PREPARATION OF 1-ALKOXYCARBONYL-3-PHENYLPROPYL DERIVATIVES KANEKA CORPORATION (JP) 1999-03-24 EP disclosed
JP-H08253497-A PEPTIDE-TYPE COMPOUND RICHTER GEDEON V G RT 1996-10-01 JP disclosed
EP-0336368-B1 N2-(1-carboxy-3-phenylpropyl)-L-lysine derivative and process of producing lysinopril using the compound KANEGAFUCHI CHEMICAL IND (JP) 1995-02-01 EP disclosed
EP-0239062-B1 N2-(1-CARBOXY-3-OXO-3-PHENYLPROPYL)-L-LYSINE COMPOUNDS AND THEIR DERIVATIVES KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1991-05-29 EP disclosed
EP-0336368-A2 N2-(1-carboxy-3-phenylpropyl)-L-lysine derivative and process of producing lysinopril using the compound KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-10-11 EP disclosed
EP-0239062-A2 N2-(1-carboxy-3-oxo-3-phenylpropyl)-L-Lysine compounds and their derivatives KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-09-30 EP disclosed
EP-0239062-A2 N2-(1-carboxy-3-oxo-3-phenylpropyl)-L-Lysine compounds and their derivatives KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-09-30 EP 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-20040147773-A1 Process for purifying n2-(1(s)-ethoxycarbonyl -3-phenylpropyl)-n6-thifluoroacetyl-l-lysine KARS1, L3MBTL1, PKN2 MME 751/4885SMN1; SMN2 1082/4885ACE 2862/4885
US-10633329-B2 Method for preparing lisinopril intermediate PKLR, PHYKPL, ACE MME 525/4885SMN1; SMN2 830/4885ACE 3/4885

“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.