SCHEMBL7148258

SCHEMBL7148258

CCC(=O)Cc1ccc(C)cc1

nearest known ligand 0.56

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.56
TDP1 Q9NUW8 1/20 0.56
HPGD P15428 4/20 0.52
CTBP2 P56545 1/20 0.50
RAB9A P51151 3/20 0.48
NPC1 O15118 2/20 0.48
KMT2A Q03164 5/20 0.46
MEN1 O00255 4/20 0.46
SMN1; SMN2 Q16637 2/20 0.44
ALDH1A1 P00352 2/20 0.44
GAA P10253 1/20 0.44
LMNA P02545 1/20 0.44
CYP2C19 P33261 1/20 0.42
VNN1 O95497 1/20 0.42
SRD5A2 P31213 1/20 0.41

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
SCHEMBL4403341 0.90 HPGD (0.51) L3MBTL1TDP1HPGDCTBP2RAB9A
SCHEMBL4940818 0.88 L3MBTL1 (0.62) L3MBTL1TDP1HPGDCTBP2RAB9A
SCHEMBL7149195 0.84 ALDH1A1 (0.52) L3MBTL1TDP1HPGDRAB9AKMT2A
SCHEMBL12770093 0.83 L3MBTL1 (0.54) L3MBTL1TDP1HPGDCTBP2RAB9A
SCHEMBL1411319 0.83 L3MBTL1 (0.62) L3MBTL1TDP1HPGDCTBP2RAB9A
SCHEMBL43309 0.82 CA2 (0.58) CTBP2RAB9ANPC1KMT2AMEN1
SCHEMBL17481548 0.82 ALDH1A1 (0.59) TDP1HPGDALDH1A1GAALMNA
SCHEMBL5539303 0.82 IAPP (0.40) L3MBTL1TDP1HPGDALDH1A1GAA
SCHEMBL8638768 0.81 L3MBTL1 (0.51) L3MBTL1TDP1HPGDCTBP2RAB9A
SCHEMBL10258480 0.81 HPGD (0.47) L3MBTL1TDP1HPGDCTBP2RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112521242-A Preparation method of 4-n-propyl-p-xylene cyclic dimer 东南大学 2021-03-19 CN claimed
CN-120136646-A Method for synthesizing benzyl alkyl ketone compound by visible light catalysis 中国科学院化学研究所 2025-06-13 CN disclosed
US-20250146144-A1 Decarboxylation Coupling Electrocatalysis Method for Catalyzing Aromatic Trimethyl Ammonium Salt and A-Nickel Ketonate CHANGZHOU INSTITUTE OF TECHNOLOGY (CN) 2025-05-08 US disclosed
US-12281400-B1 Decarboxylation coupling electrocatalysis method for catalyzing aromatic trimethyl ammonium salt and α-nickel ketonate CHANGZHOU INSTITUTE OF TECHNOLOGY (CN) 2025-04-22 US disclosed
CN-115786735-B Lithium extractant and extraction method thereof 重庆康普化学工业股份有限公司 2024-05-14 CN disclosed
CN-114956932-B Synthesis method of polysubstituted chiral tetrahydroquinoline compound 东北大学秦皇岛分校 2023-11-10 CN disclosed
US-11780833-B2 Emetine derivatives, prodrugs containing same, and methods of treating conditions using same HOWARD UNIVERSITY (US) 2023-10-10 US disclosed
CN-116324688-A Method for manufacturing conductive member for touch panel, and conductive member for touch panel 富士胶片株式会社 2023-06-23 CN disclosed
CN-115786735-A Lithium extractant and extraction method thereof 重庆康普化学工业股份有限公司 2023-03-14 CN disclosed
CN-114540848-A Decarboxylation coupling electrocatalysis method for realizing catalysis of aromatic trimethyl ammonium salt and alpha-nickel keto acid 常州工学院 2022-05-27 CN disclosed
EP-0939134-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2002-09-11 EP disclosed
US-6114582-A DECYCLIZATION TO FORM A CHEMICAL INTERMEDIATE FOR PRODUCING AN ANTI-OBESITY AGENT AND ANTIDIABETIC AGENT DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2000-09-05 US disclosed
EP-0654534-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2000-03-01 EP disclosed
EP-0939134-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-09-01 EP disclosed
EP-0924194-A2 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-06-23 EP disclosed
EP-0924193-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-06-23 EP disclosed
US-5811293-A CULTURE PRODUCT AS CHEMICAL INTERMEDIATE FOR ANTI-OBESITY AGENT DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1998-09-22 US disclosed
US-5629200-A MICROORGANISM DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1997-05-13 US disclosed
EP-0654534-A2 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1995-05-24 EP disclosed
US-3992451-A IN THE PRESENCE OF FREE RADICAL CATALYSTS, HYDROGEN CHLORIDE, AND CARBON MONOXIDE UNIVERSAL OIL PRODUCTS COMPANY (US) 1976-11-16 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-11780833-B2 Emetine derivatives, prodrugs containing same, and methods of treating conditions using same EML4, MCL1, ERAP2 L3MBTL1 189/4885TDP1 1234/4885HPGD 1325/4885

“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.