SCHEMBL899628

SCHEMBL899628

Cc1onc(-c2c(F)cccc2Cl)c1C(=O)O

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.68
SMN1; SMN2 Q16637 1/20 0.68
KMT2A Q03164 4/20 0.67
MEN1 O00255 2/20 0.67
ALDH1A1 P00352 4/20 0.66
GPBAR1 Q8TDU6 1/20 0.65
ATM Q13315 2/20 0.64
GLA P06280 1/20 0.64
HPGD P15428 1/20 0.64
HTT P42858 1/20 0.64
GAA P10253 1/20 0.63
MAPT P10636 1/20 0.63
TSHR P16473 1/20 0.62
POLB P06746 2/20 0.61
ALOX15 P16050 1/20 0.61
KDM4E B2RXH2 1/20 0.61
PPARG P37231 1/20 0.61
NCOA2 Q15596 1/20 0.61
PTGS2 P35354 1/20 0.61
NPC1 O15118 1/20 0.60

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
SCHEMBL5774873 0.90 LMNA (0.54) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL316185 0.90 ALDH1A1 (0.76) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL10520781 0.89 LMNA (0.68) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL30881266 0.89 LMNA (0.68) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL1065677 0.89 LMNA (0.68) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL7184918 0.88 TSHR (0.82) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL10332625 0.88 LMNA (0.67) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL5774615 0.87 LMNA (0.59) LMNASMN1; SMN2KMT2AMEN1ALDH1A1
SCHEMBL12457296 0.86 TSHR (0.69) LMNASMN1; SMN2KMT2AALDH1A1GPBAR1
SCHEMBL11893412 0.85 ALDH1A1 (0.72) LMNASMN1; SMN2KMT2AMEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115677607-B Isoxazole amide derivative and preparation method and application thereof 遵义医科大学 2023-10-31 CN claimed
CN-115677607-A Isoxazole amide derivative and preparation method and application thereof 遵义医科大学 2023-02-03 CN claimed
CN-109400630-B Synthetic method of flucloxacillin sodium 浙江普洛得邦制药有限公司 2021-07-02 CN claimed
CN-102964356-A Synthesis method of flucloxacillin sodium HEZE RUIZHI TECHNOLOGY DEV CO LTD 2013-03-13 CN claimed
EP-1745009-B1 HETEROARYL SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES GRUENENTHAL GMBH (DE) 2012-11-14 EP claimed
CN-100467455-C Synthetic method for 3-(2'-chloro-6'-fluorophenyl)-5-methyl-4-isooxazole formyl chloride UNIV ZHEJIANG TECHNOLOGY (CN) 2009-03-11 CN claimed
JP-2007536321-A 2007-12-13 JP claimed
CN-101016272-A Synthetic method for 3-(2'-chloro-6'-fluorophenyl)-5-methyl-4-isooxazole formyl chloride UNIV ZHEJIANG TECHNOLOGY (CN) 2007-08-15 CN claimed
US-20070129369-A1 Heteroaryl substituted cyclohexyl-1,4-diamine compounds GRUENENTHAL GMBH (DE) 2007-06-07 US claimed
EP-1745009-A1 HETEROARYL SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES Grünenthal GmbH (DE) 2007-01-24 EP claimed
WO-2005110971-A1 HETEROARYL SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES Grünenthal GmbH (DE) 2005-11-24 WO claimed
EP-1377589-B1 OXAZOLYL-PYRAZOLE DERIVATIVES AS KINASE INHIBITORS PHARMACIA ITALIA SPA (IT) 2005-09-07 EP claimed
EP-1250340-B1 METHODS AND COMPOUNDS FOR INHIBITING MRP1 LILLY CO ELI (US) 2004-11-17 EP claimed
US-20250346575-A1 ISOINDOLINONE DERIVATIVE HAVING GLUTARIMIDE MOTHER NUCLEUS, AND USE THEREOF KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2025-11-13 US disclosed
EP-4431505-A1 ISOINDOLINONE DERIVATIVE HAVING GLUTARIMIDE MOTHER NUCLEUS, AND USE THEREOF Korea Research Institute of Chemical Technology (KR) 2024-09-18 EP disclosed
CN-118234721-A Isoindolinone derivative with glutarimide mother nucleus and application thereof 韩国化学研究院 2024-06-21 CN disclosed
WO-1997005131-A1 NEW CARBOXAMIDES WITH ANTIFUNGAL ACTIVITY J. URIACH & CIA. S.A. (ES) 1997-02-13 WO disclosed
CN-1033031-C Modified gangliosides and functional derivatives thereof FIDIA SPA (IT) 1996-10-16 CN disclosed
CN-1051912-A Improved gangliosides and functional derivatives thereof FIDIA B P A (IT) 1991-06-05 CN disclosed
US-4230849-A Process for the activation of carboxylic acids ANTIBIOTICOS, S.A. (ES) 1980-10-28 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 (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-20070129369-A1 Heteroaryl substituted cyclohexyl-1,4-diamine compounds DDC, DPYD, PKD1 LMNA 2080/4885SMN1; SMN2 1685/4885KMT2A 3031/4885
US-20250346575-A1 ISOINDOLINONE DERIVATIVE HAVING GLUTARIMIDE MOTHER NUCLEUS, AND USE THEREOF CRBN, IDH1, IDH2 LMNA 2564/4885SMN1; SMN2 2400/4885KMT2A 1899/4885

“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.