SCHEMBL138306

SCHEMBL138306

O=C(CCl)OCc1ccccc1

nearest known ligand 0.68

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.68
MAPK1 P28482 1/20 0.68
L3MBTL1 Q9Y468 1/20 0.68
TDP1 Q9NUW8 3/20 0.57
KMT2A Q03164 2/20 0.57
SLC6A2 P23975 1/20 0.57
SLC6A3 Q01959 1/20 0.57
LMNA P02545 3/20 0.52
HCAR2 Q8TDS4 1/20 0.52
SMN1; SMN2 Q16637 1/20 0.51
CDC25B P30305 1/20 0.50
HTT P42858 1/20 0.49
CA12 O43570 1/20 0.47
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47
CA9 Q16790 1/20 0.47
MEN1 O00255 1/20 0.46
POLB P06746 1/20 0.46
MAPT P10636 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
SCHEMBL29079456 0.87 ALDH1A1 (0.61) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL18668857 0.87 ALDH1A1 (0.53) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL5413781 0.85 ALDH1A1 (0.59) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL523412 0.84 ALDH1A1 (0.63) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL29094173 0.84 TDP1 (0.63) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL1177836 0.83 ALDH1A1 (0.73) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL294341 0.83 ALDH1A1 (0.73) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL3730231 0.82 ALDH1A1 (0.61) ALDH1A1MAPK1L3MBTL1TDP1KMT2A
SCHEMBL3924805 0.82 MEN1 (0.53) ALDH1A1MAPK1L3MBTL1KMT2AHTT
SCHEMBL1366489 0.81 ALDH1A1 (0.59) ALDH1A1MAPK1L3MBTL1TDP1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119661458-A N-phenyl triazinone derivative and preparation method and application thereof 贵州大学 2025-03-21 CN claimed
CN-116023542-B Catalyst component, catalyst and preparation method and application thereof 中国石油化工股份有限公司 2024-09-17 CN claimed
CN-114456065-B Synthesis method of caronic acid diester compound and caronic acid derivative 上海璨谊生物科技有限公司 2024-09-13 CN claimed
CN-111386257-B Process for preparing enzalutamide using novel intermediates 阿尔第药物实验室有限公司 2024-05-24 CN claimed
CN-117466847-A Preparation method of Neofast intermediate benzofuran-6-carboxylic acid 中国医药工业研究总院有限公司 2024-01-30 CN claimed
CN-116217638-B Seleno-non-natural sugar and preparation method and application thereof 南京大学 2023-07-07 CN claimed
CN-116217638-A Seleno-non-natural sugar and preparation method and application thereof 南京大学 2023-06-06 CN claimed
CN-113717548-B Surface-modified silica gel and preparation method and application thereof 中国石油化工股份有限公司 2022-10-11 CN claimed
CN-111471041-B Synthetic method of oxazolidinone antibacterial drug intermediate 中国科学院上海药物研究所 2022-09-20 CN claimed
EP-3733648-B1 METHOD FOR PREPARING 5R-BENZYLOXYAMINOPIPERIDIN-2S-CARBOXYLIC ACID OR DERIVATIVE THEREOF XINFA PHARMACEUTICAL CO LTD (CN) 2022-06-08 EP claimed
CN-112358403-A Method for preparing pentazocine intermediate 和鼎(南京)医药技术有限公司 2021-02-12 CN claimed
EP-3733648-A1 METHOD FOR PREPARING 5R-BENZYLOXYAMINOPIPERIDIN-2S-CARBOXYLIC ACID OR DERIVATIVE THEREOF Xinfa Pharmaceutical Co., Ltd (CN) 2020-11-04 EP claimed
CN-111471041-A Synthetic method of oxazolidinone antibacterial drug intermediate 中国科学院上海药物研究所 2020-07-31 CN claimed
CN-111386257-A Process for preparing enzalutamide using novel intermediates 阿尔第实业有限公司 2020-07-07 CN claimed
CN-110078644-B preparation method of [2- [1- (Fmoc-amino) ethoxy ] acetic acid 深圳市茵诺圣生物科技有限公司 2019-12-17 CN claimed
CN-105646757-B A kind of preparation method of cationic polymerization system and high degree of unsaturation isoolefin copolymers 中国石油化工股份有限公司 2018-04-13 CN claimed
CN-105646757-A Cationic polymerization system and preparation method of high-unsaturation-degree isoolefin copolymer 中国石油化工股份有限公司 2016-06-08 CN claimed
US-20020010371-A1 Process for preparing a cyclic amino acid anticonvulsant compound DEERING CARL FRANCIS (US) 2002-01-24 US claimed
US-6294690-B1 REACTING BENZONITRILE WITH ALKALI METAL IN AMMONIA OR AMINE IN SOLVENT TO FORM ANIONIC INTERMEDIATE, ALKYLATING WITH HALOACETIC ACID, HYDROGENATING RING, HYDROGENATING NITRILE TO AMINE TO PRODUCE GABAPENTIN WARNER-LAMBERT COMPANY 2001-09-25 US claimed
WO-1999018063-A2 PROCESS FOR PREPARING A CYCLIC AMINO ACID ANTICONVULSANT COMPOUND WARNER-LAMBERT COMPANY (US) 1999-04-15 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 (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-20020010371-A1 Process for preparing a cyclic amino acid anticonvulsant compound BCAT1, BCAT2, GABRA6 ALDH1A1 2115/4885MAPK1 1986/4885L3MBTL1 3868/4885

“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.