SCHEMBL10105765

SCHEMBL10105765

CCCCOC(=O)C(Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(C)=O

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.50
THRB P10828 1/20 0.50
CYP2C9 P11712 1/20 0.50
CYP2C19 P33261 1/20 0.50
HSD17B10 Q99714 1/20 0.50
CPA1 P15085 1/20 0.48
CPB1 P15086 1/20 0.48
CPA2 P48052 1/20 0.48
CPA4 Q9UI42 1/20 0.48
ACE2 Q9BYF1 1/20 0.48
TACR1 P25103 1/20 0.47
CAPN1 P07384 3/20 0.47
PSMB5 P28074 3/20 0.47
REN P00797 2/20 0.47
GNPAT O15228 1/20 0.46

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
SCHEMBL2633286 1.00 ALDH1A1 (0.50) ALDH1A1THRBCYP2C9CYP2C19HSD17B10
SCHEMBL2632731 0.88 CPA1 (0.50) ALDH1A1CPA1CPA2CPA4PSMB5
SCHEMBL14208789 0.87 TACR1 (0.60) ALDH1A1THRBCYP2C9CYP2C19HSD17B10
SCHEMBL14208698 0.87 TACR1 (0.60) ALDH1A1THRBCYP2C9CYP2C19HSD17B10
SCHEMBL2759971 0.87 REN (0.45) ALDH1A1CPA1CPB1CPA2CPA4
SCHEMBL9486892 0.86 TACR1 (0.61) ALDH1A1TACR1GNPAT
SCHEMBL9488064 0.86 TACR1 (0.61) ALDH1A1TACR1GNPAT
SCHEMBL2633304 0.84 REN (0.43) CPA1CPB1CPA2CPA4ACE2
SCHEMBL14232442 0.84 REN (0.43) CPA1CPB1CPA2CPA4ACE2
SCHEMBL10105785 0.84 ALDH1A1 (0.57) ALDH1A1THRBCYP2C9CYP2C19HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8088741-B2 Compounds for enzyme inhibition ONYX THERAPEUTICS, INC. (US) 2012-01-03 US 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

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-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 ALDH1A1 3376/4885THRB 3055/4885CYP2C9 1918/4885

“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.