SCHEMBL367268

SCHEMBL367268

O=c1cc(-c2ccccc2)[nH]c2ccccc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 9/20 1.00
LMNA P02545 7/20 1.00
CTSV O60911 5/20 1.00
CTSL P07711 5/20 1.00
KDM4E B2RXH2 5/20 1.00
TP53 P04637 2/20 1.00
HSD17B10 Q99714 2/20 1.00
TUBB4A P04350 1/20 1.00
TUBB P07437 1/20 1.00
TUBA3C P0DPH7 1/20 1.00
TUBA1B P68363 1/20 1.00
TUBA4A P68366 1/20 1.00
TUBB4B P68371 1/20 1.00
TUBB3 Q13509 1/20 1.00
TUBB2A Q13885 1/20 1.00
TUBB8 Q3ZCM7 1/20 1.00
TUBA3E Q6PEY2 1/20 1.00
NPSR1 Q6W5P4 1/20 1.00
TUBA1A Q71U36 1/20 1.00
TUBA1C Q9BQE3 1/20 1.00

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
SCHEMBL29411863 1.00 HPGD (1.00) HPGDLMNACTSVCTSLKDM4E
Acetic Acid SCHEMBL6142950 0.92 HPGD (0.84) HPGDLMNACTSVCTSLKDM4E
SCHEMBL2630603 0.86 HPGD (0.76) HPGDLMNACTSVCTSLKDM4E
SCHEMBL6001723 0.86 CTSV (0.75) HPGDLMNACTSVCTSLKDM4E
SCHEMBL30935678 0.86 HPGD (1.00) HPGDLMNACTSVCTSLKDM4E
SCHEMBL30462938 0.86 KDM4E (1.00) HPGDLMNACTSVCTSLKDM4E
SCHEMBL311524 0.86 CTSV (0.75) HPGDLMNACTSVCTSLKDM4E
SCHEMBL6001399 0.86 CTSV (1.00) HPGDLMNACTSVCTSLKDM4E
SCHEMBL29411879 0.86 CTSV (1.00) HPGDLMNACTSVCTSLKDM4E
SCHEMBL6534180 0.86 HPGD (1.00) HPGDLMNACTSVCTSLKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220273608-A1 Methods for Treating Bone-Related Disorders UNIVERSITY OF MARYLAND, BALTIMORE (US) 2022-09-01 US claimed
US-20190351055-A1 Methods for Treating Bone-Related Disorders UNIVERSITY OF BALTIMORE, MARYLAND (US) 2019-11-21 US claimed
EP-3541474-A1 METHODS FOR TREATING BONE-RELATED DISORDERS University Of Maryland, Baltimore (US) 2019-09-25 EP claimed
CN-109516976-A The crystal form and preparation method thereof of substituted uracil PI3K inhibitor mesylate 南京圣和药业股份有限公司 2019-03-26 CN claimed
WO-2018094059-A1 METHODS FOR TREATING BONE-RELATED DISORDERS UNIVERSITY OF MARYLAND, BALTIMORE (US) 2018-05-24 WO claimed
US-9511117-B2 Treatment of muscular conditions and muscular dystrophies UNIVERSITY OF MARYLAND, BALTIMORE (US) 2016-12-06 US claimed
US-9029394-B2 2-phenyl-4-quinolones as anticancer agents CHINA MEDICAL UNIVERSITY (TW) 2015-05-12 US claimed
US-20140256644-A1 Treatment of Muscular Conditions and Muscular Dystrophies NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2014-09-11 US claimed
EP-2455369-B1 Derivatives of 2-aryl-4-quinolones having an aminoalkyl group as anticancer agents UNIV CHINA MEDICAL (TW) 2014-09-03 EP claimed
US-20130252999-A1 2-PHENYL-4-QUINOLONES AS ANTICANCER AGENTS CHINA MEDICAL UNIVERSITY (TW) 2013-09-26 US claimed
US-20100168064-A1 NOVEL HYDROPHILIC DERIVATIVES OF 2-ARYL-4-QUINOLONES AS ANTICANCER AGENTS CHINA MEDICAL UNIVERSITY (TW) 2010-07-01 US claimed
CN-101583280-A Novel hydrophilic derivatives of 2-aryl-4-quinolones as anticancer agents UNIV CHINA MEDICAL (CN) 2009-11-18 CN claimed
EP-2096924-A1 NOVEL HYDROPHILIC DERIVATIVES OF 2-ARYL-4-QUINOLONES AS ANTICANCER AGENTS China Medical University (TW) 2009-09-09 EP claimed
WO-2008070176-A1 NOVEL HYDROPHILIC DERIVATIVES OF 2-ARYL-4-QUINOLONES AS ANTICANCER AGENTS CHINA MEDICAL UNIVERSITY (TW) 2008-06-12 WO claimed
JP-2002522388-A 2002-07-23 JP claimed
EP-1107759-A1 PYRIDINONES FOR THE TREATMENT OF SEXUAL DYSFUNCTION Basf Corporation (US) 2001-06-20 EP claimed
WO-2000035865-A2 TUBULIN-BINDING AGENTS TULARIK INC. (US) 2000-06-22 WO claimed
WO-2000007595-A1 PYRIDINONES FOR THE TREATMENT OF SEXUAL DYSFUNCTION BASF CORPORATION (US) 2000-02-17 WO claimed
US-5571822-A AMINO-2-PHENYL-4-QUINOLONE DERIVATIVES THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 1996-11-05 US claimed
WO-1996010563-A1 2-ARYL-4-QUINOLONES AS ANTITUMOR COMPOUNDS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 1996-04-11 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 (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-20100168064-A1 NOVEL HYDROPHILIC DERIVATIVES OF 2-ARYL-4-QUINOLONES AS ANTICANCER AGENTS DHX30, SLC20A2, DDX20 HPGD 1886/4885LMNA 4383/4885CTSV 4217/4885
US-20130252999-A1 2-PHENYL-4-QUINOLONES AS ANTICANCER AGENTS PPIP5K2, DDX5, DHX30 HPGD 2307/4885LMNA 4539/4885CTSV 4417/4885

“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.