SCHEMBL307892

SCHEMBL307892

COC(=O)c1cccc(CN)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LOXL2 Q9Y4K0 3/20 1.00
CYP4F2 P78329 2/20 0.68
CYP4A11 Q02928 2/20 0.68
SLC7A5 Q01650 1/20 0.63
MRGPRX4 Q96LA9 2/20 0.55
ALDH1A1 P00352 3/20 0.54
KDM4E B2RXH2 1/20 0.54
MAPT P10636 1/20 0.54
RAB9A P51151 1/20 0.54
SMN1; SMN2 Q16637 1/20 0.54
HIF1A Q16665 1/20 0.52
TSHR P16473 1/20 0.52
HPGD P15428 1/20 0.51
FOLH1 Q04609 1/20 0.51
LOX P28300 1/20 0.50
HTR2C P28335 1/20 0.50
MEN1 O00255 1/20 0.50
NPC1 O15118 1/20 0.50
KMT2A Q03164 1/20 0.50

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
SCHEMBL29451790 1.00 LOXL2 (1.00) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
Hydrochloric Acid SCHEMBL307062 0.98 LOXL2 (0.97) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
Hydrochloric Acid SCHEMBL307891 0.98 LOXL2 (0.97) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
SCHEMBL27405638 0.90 LOXL2 (0.82) LOXL2CYP4F2CYP4A11SLC7A5
SCHEMBL3012713 0.86 LOXL2 (0.76) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
SCHEMBL126284 0.85 LOXL2 (0.74) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
SCHEMBL70173 0.85 CYP4F2 (0.83) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
Hydrochloric Acid SCHEMBL4447485 0.85 LOXL2 (0.73) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
SCHEMBL95887 0.84 LOXL2 (0.72) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4
SCHEMBL31276630 0.84 CYP4F2 (0.75) LOXL2CYP4F2CYP4A11SLC7A5MRGPRX4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250388584-A1 TPK AGONIST AND METHOD FOR TREATING NEURODEGENERATIVE DISEASES USING SAME SHANGHAI RAISING PHARMACEUTICAL CO LTD (CN) 2025-12-25 US disclosed
EP-4663630-A1 NOVEL BENZIMIDAZOLONE DERIVATIVE COMPOUND AS AUTOTAXIN INHIBITOR LG Chem, Ltd. (KR) 2025-12-17 EP disclosed
WO-2025213277-A1 N1-(3,4-DICHLOROPHENYL)MALEAMIDE DERIVATIVES AND THE USE THEREOF IN THE TREATMENT OF INFLAMMATORY DISORDERS THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2025-10-16 WO disclosed
EP-4556007-A1 TPK AGONIST AND METHOD FOR TREATING NEURODEGENERATIVE DISEASES USING SAME Shanghai Raising Pharmaceutical Co., Ltd. (CN) 2025-05-21 EP disclosed
CN-115806503-B Selective histone deacetylase inhibitor and preparation method and application thereof 中国海洋大学 2025-03-07 CN disclosed
US-12195472-B2 Substituted indole Mcl-1 inhibitors VANDERBILT UNIVERSITY (US) 2025-01-14 US disclosed
CN-113563245-B Substituted pyrrolidines and their use in medicine 广东东阳光药业股份有限公司 2024-10-15 CN disclosed
WO-2024201308-A1 NOVEL BENZIMIDAZOLONE DERIVATIVE COMPOUND AS AUTOTAXIN INHIBITOR 주식회사 엘지화학 2024-10-03 WO disclosed
EP-3784226-B1 PYRAZOLE-PHENYLAMIDE DERIVATIVES AS INHIBITORS OF THE RHO-ASSOCIATED PROTEIN KINASE ROCK1 AND ROCK2 FOR THE TREATMENT OF CANCER TRANSLATIONAL DRUG DEV LLC (US) 2024-08-14 EP disclosed
CN-112367982-B Amide compounds, compositions and methods of treatment as kinase inhibitors 转化药物开发有限责任公司 2024-05-07 CN disclosed
EP-1192177-A1 STATINE-DERIVED TETRAPEPTIDE INHIBITORS OF BETA-SECRETASE Elan Pharmaceuticals, Inc. (US) 2002-04-03 EP disclosed
EP-0775133-B1 NAPHTHALENE AMIDES HAVING LEUKOTRIENE-ANTAGONISTIC ACTION MENARINI LAB (ES) 2001-05-30 EP disclosed
WO-2000077030-A1 STATINE-DERIVED TETRAPEPTIDE INHIBITORS OF BETA-SECRETASE ELAN PHARMACEUTICALS, INC. (US) 2000-12-21 WO disclosed
WO-1999012912-A1 THIOUREA DERIVATIVES OR NON-TOXIC SALTS THEREOF FOR INHIBITNG RAS-TRANSFORMED CELL GROWTH YUHAN CORPORATION (KR) 1999-03-18 WO disclosed
EP-0817630-A4 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE MERCK & CO INC (US) 1999-01-27 EP disclosed
EP-0817630-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE Merck & Co., Inc. (US) 1998-01-14 EP disclosed
US-5578629-A ANTICARCINOGENIC AGENTS MERCK & CO., INC. (US) 1996-11-26 US disclosed
WO-1996030015-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE MERCK & CO., INC. (US) 1996-10-03 WO disclosed
US-5534537-A Prodrugs of inhibitors of farnesyl-protein transferase MERCK & CO., INC. (US) 1996-07-09 US disclosed
WO-1996004267-A1 NAPHTHALENE AMIDES HAVING LEUKOTRIENE-ANTAGONISTIC ACTION LABORATORIOS MENARINI S.A. (ES) 1996-02-15 WO 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-12195472-B2 Substituted indole Mcl-1 inhibitors MCL1, BCL2L1, BCL3 LOXL2 1051/4885CYP4F2 4608/4885CYP4A11 4537/4885
US-20250388584-A1 TPK AGONIST AND METHOD FOR TREATING NEURODEGENERATIVE DISEASES USING SAME PDXK, SLC19A2, NADK LOXL2 2861/4885CYP4F2 821/4885CYP4A11 997/4885

“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.