SCHEMBL217352

SCHEMBL217352

CC(C)C[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O)C(C)C

nearest known ligand 0.60

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
FOLH1 Q04609 1/20 0.60
ACE P12821 7/20 0.56
NPY1R P25929 1/20 0.56
NPY2R P49146 1/20 0.56
NPY4R P50391 1/20 0.56
MME P08473 3/20 0.53
CPA1 P15085 2/20 0.53
ACE2 Q9BYF1 2/20 0.53
BACE1 P56817 6/20 0.51
BACE2 Q9Y5Z0 2/20 0.51
OPRM1 P35372 1/20 0.49
OPRD1 P41143 1/20 0.49

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
SCHEMBL73897 0.97 NPY4R (0.60) FOLH1ACENPY1RNPY2RNPY4R
SCHEMBL11056714 0.93 FOLH1 (0.69) FOLH1ACENPY1RNPY2RNPY4R
SCHEMBL2474675 0.93 FOLH1 (0.69) FOLH1ACENPY1RNPY2RNPY4R
SCHEMBL31067318 0.93 FOLH1 (0.69) FOLH1ACENPY1RNPY2RNPY4R
SCHEMBL31636210 0.92 BACE1 (0.55) FOLH1ACENPY1RNPY2RNPY4R
SCHEMBL30464728 0.92 NPY1R (0.60) FOLH1ACENPY1RNPY2RNPY4R
Hydrochloric Acid SCHEMBL6473764 0.92 FOLH1 (0.67) FOLH1ACENPY1RNPY2RNPY4R
SCHEMBL32681297 0.91 FOLH1 (0.60) FOLH1ACENPY1RNPY2RNPY4R
SCHEMBL30445563 0.91 OPRD1 (0.54) FOLH1ACEMMECPA1ACE2
SCHEMBL30445840 0.91 OPRD1 (0.54) FOLH1ACEMMECPA1ACE2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220267372-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION ONYX PHARMACEUTICALS, INC. 2022-08-25 US disclosed
WO-2022170196-A1 BINDING PEPTIDES AND USES THEREOF THE JOHNS HOPKINS UNIVERSITY (US) 2022-08-11 WO disclosed
US-20210179663-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PROTEOLIX, INC. 2021-06-17 US disclosed
US-20200325172-A1 Compounds for proteasome enzyme inhibition PROTEOLIX, INC. 2020-10-15 US disclosed
US-20200071356-A1 COMPOUNDS FOR PROTEASOME PROTEOLIX, INC. 2020-03-05 US disclosed
US-20190211058-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PROTEOLIX, INC. 2019-07-11 US disclosed
US-10150794-B2 Compounds for enzyme inhibition ONYX THERAPEUTICS, INC. (US) 2018-12-11 US disclosed
US-20180170962-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION ONYX THERAPEUTICS INC (US) 2018-06-21 US disclosed
EP-3101026-B1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION ONYX THERAPEUTICS INC (US) 2018-03-28 EP disclosed
US-20170260230-A1 COMPUNDS FOR ENZYME INHIBITION ONYX THERAPEUTICS INC (US) 2017-09-14 US disclosed
US-7417042-B2 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2008-08-26 US disclosed
EP-1948678-A1 COMPOUNDS FOR ENZYME INHIBITION Proteolix, Inc. (US) 2008-07-30 EP disclosed
US-20080090785-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2008-04-17 US disclosed
WO-2007056464-A1 COMPOUNDS FOR ENZYME INHIBITION PROTEOLIX, INC. (US) 2007-05-18 WO disclosed
US-20070105786-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2007-05-10 US disclosed
EP-1781688-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION Proteolix, Inc. (US) 2007-05-09 EP disclosed
EP-1758921-A2 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION Proteolix, Inc. (US) 2007-03-07 EP disclosed
WO-2006017842-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PROTEOLIX, INC. (US) 2006-02-16 WO disclosed
US-20060030533-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2006-02-09 US disclosed
WO-2005111008-A2 COMPOUNDS FOR ENZYME INHIBITION PROTEOLIX, INC. (US) 2005-11-24 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 (11 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-20220267372-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB11 FOLH1 1692/4885ACE 315/4885NPY1R 3368/4885
US-20180170962-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB3 FOLH1 1772/4885ACE 347/4885NPY1R 3351/4885
US-20200071356-A1 COMPOUNDS FOR PROTEASOME PSMB1, PSMB9, PSMB2 FOLH1 2012/4885ACE 918/4885NPY1R 3789/4885
US-20080090785-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents ANPEP, DNPEP, CPN1 FOLH1 1094/4885ACE 484/4885NPY1R 2267/4885
US-20070105786-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents ANPEP, PSMB1, PSMB3 FOLH1 1285/4885ACE 611/4885NPY1R 3068/4885
US-20200325172-A1 Compounds for proteasome enzyme inhibition PSMB1, PSMB9, PSMB3 FOLH1 1772/4885ACE 347/4885NPY1R 3351/4885
US-20190211058-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB3 FOLH1 1772/4885ACE 347/4885NPY1R 3351/4885
US-20170260230-A1 COMPUNDS FOR ENZYME INHIBITION ANPEP, PSMB1, CPN1 FOLH1 693/4885ACE 527/4885NPY1R 4037/4885
US-20210179663-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB3 FOLH1 1772/4885ACE 347/4885NPY1R 3351/4885
US-10150794-B2 Compounds for enzyme inhibition ANPEP, HPN, DNPEP FOLH1 873/4885ACE 433/4885NPY1R 3660/4885
US-20060030533-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents ANPEP, DNPEP, CPN1 FOLH1 1100/4885ACE 479/4885NPY1R 2271/4885

“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.