SCHEMBL805648

SCHEMBL805648

COC(=O)[C@H](C)NC(C)=O

nearest known ligand 0.50

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CA14 Q9ULX7 1/20 0.50
TSHR P16473 4/20 0.43
MEN1 O00255 3/20 0.43
KMT2A Q03164 3/20 0.43
SMN1; SMN2 Q16637 2/20 0.42
MAPT P10636 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
GAA P10253 1/20 0.41
RECQL P46063 1/20 0.41
ALDH1A1 P00352 3/20 0.40
KDM4E B2RXH2 1/20 0.40
HPGD P15428 1/20 0.40
MAPK1 P28482 1/20 0.39
BIRC2 Q13490 1/20 0.38
LMNA P02545 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
SCHEMBL1884920 1.00 CA14 (0.50) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL1876220 1.00 CA14 (0.50) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL20393857 0.91 CA14 (0.43) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL21738188 0.91 CA14 (0.43) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL13645819 0.91 CA14 (0.43) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL7776379 0.91 CA14 (0.43) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL11664935 0.81 CA14 (0.52) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL30493714 0.81 MEN1 (0.44) CA14TSHRMEN1KMT2ASMN1; SMN2
SCHEMBL5808282 0.80 TSHR (0.46) CA14TSHRSMN1; SMN2MAPTGAA
SCHEMBL21488518 0.80 GAA (0.39) CA14TSHRMEN1KMT2ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2006119283-A2 ANTI-ODOR COMPOSITIONS AND THERAPEUTIC USE YU RUEY J (US) 2006-11-09 WO claimed
US-20060251597-A1 ANTI-ODOR COMPOSITIONS AND THERAPEUTIC USE YU RUEY J 2006-11-09 US claimed
US-20250083136-A1 METHODS AND SYSTEMS FOR MODIFYING SELECTIVITY IN CATALYTIC REACTIONS U.S. DEPARTMENT OF ENERGY 2025-03-13 US disclosed
EP-4425181-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE Bertis Inc (KR) 2024-09-04 EP disclosed
CN-114105801-B Process for preparing Ac-AA-OR 成都郑源生化科技有限公司 2024-07-09 CN disclosed
US-20240011979-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTES BERTIS INC. (KR) 2024-01-11 US disclosed
US-20230365525-A1 ANTIVIRAL COMPOUNDS ENANTA PHARMACEUTICALS, INC. 2023-11-16 US disclosed
CN-116829949-A Compositions for detecting or measuring analytes 伯蒂斯有限公司 2023-09-29 CN disclosed
WO-2023181844-A1 VIRAL INFECTION INHIBITOR, VIRAL INFECTION INHIBITING MEMBER, AND VIRAL INFECTION INHIBITING PAINT 積水化学工業株式会社 2023-09-28 WO disclosed
WO-2023075435-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE 주식회사 베르티스 2023-05-04 WO disclosed
US-20220283131-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTES BERTIS CO., LTD. (KR) 2022-09-08 US disclosed
WO-1993001199-A1 CHIRAL PHOSPHOLANES VIA CHIRAL 1,4-DIOL CYCLIC SULFATES E.I. DU PONT DE NEMOURS AND COMPANY (US) 1993-01-21 WO disclosed
US-5171892-A Chiral phospholanes via chiral 1,4-diol cyclic sulfates E. I. DU PONT DE NEMOURS AND COMPANY (US) 1992-12-15 US disclosed
EP-0498507-A1 Process for the preparation of enantiomers of alpha-amino acid derivatives by asymmetric hydrogenation DSM N.V. (NL) 1992-08-12 EP disclosed
US-5053426-A Enzyme inhibitors AMERICAN CYANAMID COMPANY (US) 1991-10-01 US disclosed
US-4962357-A Two-dimensional method for spectral editing of NMR signals produced by metabolites containing coupled spins CONTINENTAL AIRLINES, INC. 1990-10-09 US disclosed
EP-0349894-A2 Two dimensional method for spectral editing of NMR signals produced by metabolites containing coupled spins GENERAL ELECTRIC COMPANY (US) 1990-01-10 EP disclosed
EP-0076917-B1 PROCESS FOR MAKING N-ACETYL-2,3-DEHYDROAMINOCARBOXYLIC-ACID ESTERS Degussa Aktiengesellschaft (DE) 1985-04-17 EP disclosed
EP-0076917-A2 Process for making N-acetyl-2,3-dehydroaminocarboxylic-acid esters Degussa Aktiengesellschaft (DE) 1983-04-20 EP disclosed
US-RE29843-E Substituted thiazoles and flavoring processes and products produced thereby INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) 1978-11-21 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 (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-20250083136-A1 METHODS AND SYSTEMS FOR MODIFYING SELECTIVITY IN CATALYTIC REACTIONS HMBS, UNG, MPG CA14 1283/4885TSHR 2763/4885MEN1 1968/4885
US-20230365525-A1 ANTIVIRAL COMPOUNDS ACE, ZC3HAV1, SARS1 CA14 1443/4885TSHR 3807/4885MEN1 1046/4885

“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.