SCHEMBL637241

SCHEMBL637241

O=C(O)[C@](O)(C(=O)c1ccccc1)[C@](O)(C(=O)O)C(=O)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES1 P23141 7/20 0.58
SRC P12931 1/20 0.52
CES2 O00748 4/20 0.50
TSHR P16473 2/20 0.50
ALDH1A1 P00352 2/20 0.50
DAO P14920 1/20 0.50
NAPRT Q6XQN6 1/20 0.50
TDP1 Q9NUW8 4/20 0.46
MAPT P10636 3/20 0.46
CYP3A4 P08684 2/20 0.46
CA2 P00918 2/20 0.46
CA4 P22748 2/20 0.46
HSD17B10 Q99714 2/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA9 Q16790 2/20 0.46
POLB P06746 1/20 0.46
PARP1 P09874 1/20 0.46
CYP2C19 P33261 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
SCHEMBL414466 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL31097912 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL2904552 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL32681153 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL7684 1.00 CES1 (0.58) CES1SRCCES2TSHRALDH1A1
SCHEMBL11542843 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Water SCHEMBL18124365 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Water SCHEMBL19283519 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Ammonia Solution, Strong SCHEMBL11444696 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1
Ammonia Solution, Strong SCHEMBL11444694 0.97 CES1 (0.56) CES1SRCCES2TSHRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250388579-A1 SYNTHESIS OF KRAS G12C INHIBITOR COMPOUND AMGEN INC. (US) 2025-12-25 US claimed
US-12473281-B2 Synthesis of KRAS G12C inhibitor compound AMGEN INC. (US) 2025-11-18 US claimed
US-20250206736-A1 SYNTHESIS OF KRAS G12C INHIBITOR COMPOUND AMGEN INC. (US) 2025-06-26 US claimed
US-20240376102-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF RUXOLITINIB PHOSPHATE NATCO PHARMA LIMITED (IN) 2024-11-14 US claimed
WO-2024130425-A1 METHODS OF MAKING 2-AMINO-L-(3-HYDROXY-2,6-DIMETHYLPHENYL)-5,6- DIMETHYL-LH-PYRROLO-[2,3-B]PYRIDINE-3-CARBOXAMIDE, A MYTL INHIBITOR REPARE THERAPEUTICS INC. (CA) 2024-06-27 WO claimed
US-11999741-B2 Process for the synthesis of 6-((3S,4S)-4-methyl-1-(pyrimidin-2-ylmethyl)pyrrolidin-3-yl)-3-(tetrahydropyran-4-yl-7H-imidazo[1,5-a]pyrazin-8-one CARDURION PHARMACEUTICALS, INC. (US) 2024-06-04 US claimed
US-20230122169-A1 NOVEL METHOD FOR PREPARING (-)-CIBENZOLINE SUCCINATE CELLTRION, INC. (KR) 2023-04-20 US claimed
WO-2023042224-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF RUXOLITINIB PHOSPHATE NATCO PHARMA LIMITED (IN) 2023-03-23 WO claimed
US-20220162233-A1 PROCESSES AND COMPOUNDS RADIUS HEALTH, INC. 2022-05-26 US claimed
EP-3924328-A1 PROCESSES AND COMPOUNDS Radius Pharmaceuticals, Inc. (US) 2021-12-22 EP claimed
US-20100331544-A1 METHOD FOR PRODUCING (1R,5S) ANHYDROECGONINE ESTER SALTS BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2010-12-30 US claimed
CN-101130520-B Novel method for splitting and producing natural (-)-huperzine and non- natural (+)-huperzine by racemate of diastereoisomer salt SHANGHAI INST MATERIA MEDICA 2010-05-12 CN claimed
US-7629466-B2 Synthetic methods and intermediates for steroisomeric compounds useful for the treatment of gastrointestinal and central nervous system disorders ARYX THERAPEUTICS, INC. (US) 2009-12-08 US claimed
US-20090137810-A1 Synthetic Methods and Intermediates for Stereoisomeric Compounds Useful for the Treatment of Gastrointestinal and Central Nervous System Disorders ARYX THERAPEUTICS, INC. (US) 2009-05-28 US claimed
CN-101258151-A Process for the synthesis of stereoisomeric compounds useful in the treatment of gastrointestinal and central nervous system disorders and intermediates ARYX THERAPEUTICS INC (US) 2008-09-03 CN claimed
EP-1919909-A2 SYNTHETIC METHODS AND INTERMEDIATES FOR STEREOISOMERIC COMPOUNDS USEFUL FOR THE TREATMENT OF GASTROINTESTINAL AND CENTRAL NERVOUS SYSTEM DISORDERS Aryx Therapeutics, Inc. (US) 2008-05-14 EP claimed
CN-101130520-A Novel method for splitting and producing natural (-)-huperzine and non- natural (+)-huperzine by racemate of diastereoisomer salt SHANGHAI INST MATERIA MEDICA (CN) 2008-02-27 CN claimed
US-7326787-B2 Synthetic methods and intermediates for stereoisomeric compounds useful for the treatment of gastrointestinal and central nervous system disorders ARYX THERAPEUTICS, INC. (US) 2008-02-05 US claimed
US-20070078265-A1 Synthetic Methods and Intermediates for Stereoisomeric Compounds Useful for the Treatment of Gastrointestinal and Central Nervous System Disorders ARYX THERAPEUTICS (US) 2007-04-05 US claimed
WO-2007028073-A2 SYNTHETIC METHODS AND INTERMEDIATES FOR STEREOISOMERIC COMPOUNDS USEFUL FOR THE TREATMENT OF GASTROINTESTINAL AND CENTRAL NERVOUS SYSTEM DISORDERS ARYX THERAPEUTICS, INC. (US) 2007-03-08 WO claimed

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-11999741-B2 Process for the synthesis of 6-((3S,4S)-4-methyl-1-(pyrimidin-2-ylmethyl)pyrrolidin-3-yl)-3-(tetrahydropyran-4-yl-7H-imidazo[1,5-a]pyrazin-8-one CDK8, PRMT8, RPS8 CES1 3892/4885SRC 644/4885CES2 3738/4885
US-20100331544-A1 METHOD FOR PRODUCING (1R,5S) ANHYDROECGONINE ESTER SALTS GNE, ABHD5, GALE CES1 241/4885SRC 3552/4885CES2 523/4885
US-20230122169-A1 NOVEL METHOD FOR PREPARING (-)-CIBENZOLINE SUCCINATE SDHA, SDHB, ALDH5A1 CES1 901/4885SRC 2768/4885CES2 1565/4885
US-20240376102-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF RUXOLITINIB PHOSPHATE JAK1, JAK2, FLT3 CES1 3169/4885SRC 300/4885CES2 4771/4885
US-12473281-B2 Synthesis of KRAS G12C inhibitor compound KRAS, NRAS, HRAS CES1 4624/4885SRC 992/4885CES2 4884/4885
US-20220162233-A1 PROCESSES AND COMPOUNDS ESR1, ESR2, CYP19A1 CES1 191/4885SRC 1526/4885CES2 545/4885
US-20250206736-A1 SYNTHESIS OF KRAS G12C INHIBITOR COMPOUND KRAS, NRAS, HRAS CES1 4624/4885SRC 992/4885CES2 4884/4885
US-20090137810-A1 Synthetic Methods and Intermediates for Stereoisomeric Compounds Useful for the Treatment of Gastrointestinal and Central Nervous System Disorders CCKBR, GRPR, HRH2 CES1 692/4885SRC 4395/4885CES2 787/4885
US-20070078265-A1 Synthetic Methods and Intermediates for Stereoisomeric Compounds Useful for the Treatment of Gastrointestinal and Central Nervous System Disorders CCKBR, GRPR, HRH2 CES1 692/4885SRC 4395/4885CES2 787/4885
US-20250388579-A1 SYNTHESIS OF KRAS G12C INHIBITOR COMPOUND KRAS, NRAS, BRAF CES1 2590/4885SRC 236/4885CES2 4854/4885

“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.