SCHEMBL1747843

SCHEMBL1747843

CCC(C(=O)O)N1CCCC1=O

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.75
CA12 O43570 1/20 0.75
CA1 P00915 1/20 0.75
CA2 P00918 1/20 0.75
CA3 P07451 1/20 0.75
CA4 P22748 1/20 0.75
CA6 P23280 1/20 0.75
CA5A P35218 1/20 0.75
CA7 P43166 1/20 0.75
CA9 Q16790 1/20 0.75
CA13 Q8N1Q1 1/20 0.75
CA14 Q9ULX7 1/20 0.75
CA5B Q9Y2D0 1/20 0.75
CHRM2 P08172 2/20 0.43
CHRM4 P08173 2/20 0.43
CHRM5 P08912 2/20 0.43
CHRM1 P11229 2/20 0.43
CHRM3 P20309 2/20 0.43
ACE P12821 1/20 0.39
PIK3CD O00329 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
SCHEMBL2079098 1.00 LMNA (0.75) LMNACA12CA1CA2CA3
SCHEMBL1877216 1.00 LMNA (0.75) LMNACA12CA1CA2CA3
SCHEMBL4942841 0.86 LMNA (0.61) LMNACA12CA1CA2CA3
SCHEMBL19139156 0.86 LMNA (0.61) LMNACA12CA1CA2CA3
SCHEMBL13788532 0.86 LMNA (0.75) LMNACA12CA1CA2CA3
Levetiracetam SCHEMBL118843 0.86 LMNA (1.00) LMNACA12CA1CA2CA3
SCHEMBL13788510 0.86 LMNA (0.75) LMNACA12CA1CA2CA3
Etiracetam SCHEMBL373194 0.86 LMNA (1.00) LMNACA12CA1CA2CA3
Levetiracetam SCHEMBL5072485 0.86 LMNA (1.00) LMNACA12CA1CA2CA3
Levitiracetam SCHEMBL61493 0.86 LMNA (1.00) LMNACA12CA1CA2CA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115734964-B Levetiracetam Process for the preparation of intermediates 浙江华海药业股份有限公司 2025-04-01 CN claimed
WO-2024258522-A1 PROCESS FOR THE PRODUCTION OF LEVETIRACETAM AND INTERMEDIATES THEREOF SUZHOU BRIGHTHOPE PHARMATECH CO., LTD (CN) 2024-12-19 WO claimed
CN-118050445-A Method for detecting glycerol parahydroxybenzoate in levetiracetam oral liquid 湖南省湘中制药有限公司 2024-05-17 CN claimed
CN-118028275-A Lactamase mutant for amide synthesis and application thereof 江南大学 2024-05-14 CN claimed
CN-117867528-A Method for preparing levetiracetam drug intermediate by electrocatalytic oxidation of manganese-doped nickel selenide catalyst 浙江工业大学 2024-04-12 CN claimed
CN-117677605-A Process for preparing levetiracetam and intermediates thereof 维生源知识产权有限责任公司 2024-03-08 CN claimed
EP-4329929-A2 GAS-LIQUID-SOLID AND LIQUID-SOLID REACTOR CASCADE FOR CARRYING OUT CONTINUOUS-FLOW CHEMICAL REACTIONS UNDER HIGH PRESSURE AND/OR HIGH TEMPERATURE IPSOMEDIC (FR) 2024-03-06 EP claimed
CN-113272275-B Preparation method of levetiracetam intermediate 浙江华海药业股份有限公司 2024-01-12 CN claimed
CN-116837047-A Method for preparing (S) -alpha-ethyl-2-oxo-1-pyrrolidine acetic acid 浙江华海药业股份有限公司 2023-10-03 CN claimed
CN-116655513-A Preparation method of high-purity levetiracetam 重庆圣华曦药业股份有限公司 2023-08-29 CN claimed
US-20090069575-A1 Process For The Preparation Of (S)-Alpha-Ethyl-2-Oxo-1-Pyrrolidineacetamide And (R)- Alpha-Ethyl-2-Oxo-Pyrrolidineacetamide APOTEX PHARMACHEM INC. (CA) 2009-03-12 US claimed
CN-101333180-A Method for preparing levetiracetam intermediate ZHEJIANG HUAHAI PHARM CO LTD (CN) 2008-12-31 CN claimed
CN-101270070-A Method for preparing (S)-alpha-ethyl-2-oxo--1-pyrrolidine ethanamide with high optical purity SHANGHAI ECUST BIOMEDICINE CO (CN) 2008-09-24 CN claimed
EP-1828120-A1 IMPROVED PROCESS FOR THE PREPARATION OF (S)-ALPHA-ETYL-2-OXO-1-PYRROLIDINEACETAMIDE AND (R)-ALPHA-ETHYL-2-OXO-1-PYRROLIDINEACETAMIDE Apotex Pharmachem Inc. (CA) 2007-09-05 EP claimed
WO-2006127300-A1 SYNTHESIS OF (S)-α-ETHYL-2-OXO-1-PYRROLIDINEACETAMIDE CAMBREX CHARLES CITY, INC. (US) 2006-11-30 WO claimed
WO-2006053441-A1 IMPROVED PROCESS FOR THE PREPARATION OF (S)-ALPHA-ETYL-2-OXO-1-PYRROLIDINEACETAMIDE AND (R)-ALPHA-ETHYL-2-OXO-1-PYRROLIDINEACETAMIDE APOTEX PHARMACHEM INC. (CA) 2006-05-26 WO claimed
CN-1015541-B PROCESS FOR PREPARING (S)-ALPHA-ETHYL-2-OXO-1-PYRROLIDINEACETAMIDE UCB SA (BE) 1992-02-19 CN claimed
CN-1015542-B Process for the preparation of -alpha-ethyl-2-oxo-1-pyrrolidineacetamide UCB SA (BE) 1992-02-19 CN claimed
CN-85105301-A (S)-preparation method of alpha-ethyl-2-oxo-1-pyrrolidine acetamide 1987-01-14 CN claimed
CN-85105307-A (R)-preparation method of alpha-ethyl-2-oxo-1-pyrrolidine acetamide 1987-01-14 CN 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 (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-20090069575-A1 Process For The Preparation Of (S)-Alpha-Ethyl-2-Oxo-1-Pyrrolidineacetamide And (R)- Alpha-Ethyl-2-Oxo-Pyrrolidineacetamide RPS4X, BRIX1, RIOX2 LMNA 3526/4885CA12 1708/4885CA1 846/4885

“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.