SCHEMBL250301

SCHEMBL250301

CC(=O)Oc1cccc2cccnc12

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.65
METAP2 P50579 1/20 0.65
METAP1 P53582 1/20 0.65
HDAC6 Q9UBN7 1/20 0.65
KDM4E B2RXH2 8/20 0.61
POLB P06746 2/20 0.61
L3MBTL1 Q9Y468 5/20 0.61
HSP90AA1 P07900 1/20 0.60
CYP3A4 P08684 1/20 0.59
ALOX12 P18054 1/20 0.59
TDP1 Q9NUW8 1/20 0.59
USP2 O75604 1/20 0.58
NPSR1 Q6W5P4 4/20 0.57
MEN1 O00255 2/20 0.57
KMT2A Q03164 2/20 0.57
ALOX15 P16050 1/20 0.57
HTT P42858 1/20 0.57
SMN1; SMN2 Q16637 2/20 0.56
GAA P10253 1/20 0.56
ALDH1A1 P00352 3/20 0.54

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
Butanedione SCHEMBL5530736 0.98 LMNA (0.63) LMNAMETAP2METAP1HDAC6KDM4E
Hydrochloric Acid SCHEMBL2563239 0.98 LMNA (0.63) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL19733333 0.87 LMNA (0.51) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL28459061 0.86 LMNA (0.69) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL2839930 0.85 LMNA (0.60) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL3415803 0.84 LMNA (0.71) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL7364217 0.83 L3MBTL1 (0.62) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL3454629 0.83 LMNA (0.61) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL111242 0.83 LMNA (0.65) LMNAMETAP2METAP1HDAC6KDM4E
SCHEMBL10356985 0.83 LMNA (0.65) LMNAMETAP2METAP1HDAC6KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113292492-A Method for preparing clioquinol and diiodoquinol by one-pot method 常州工程职业技术学院 2021-08-24 CN claimed
CN-111018779-A 2- (3-isoquinolyl) -ethyl propionate derivative and synthetic method thereof 中国科学院大连化学物理研究所 2020-04-17 CN claimed
EP-2935198-B1 METHOD FOR STABILISING POLYMERISABLE COMPOUNDS BASF SE (DE) 2019-06-05 EP claimed
EP-2984070-B1 N-HALOALKYLINDOLINE INTERMEDIATES, THEIR PROCESS AND USE IN PREPARATION OF SILODOSIN AND ITS DERIVATIVES MANKIND PHARMA LTD (IN) 2018-01-17 EP claimed
EP-3143055-A2 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP Bridgestone Corporation (JP) 2017-03-22 EP claimed
US-9206109-B2 Method of stabilizing polymerizable compounds BASF SE (DE) 2015-12-08 US claimed
WO-2015175280-A2 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP BRIDGESTONE CORPORATION (JP) 2015-11-19 WO claimed
EP-2935198-A2 METHOD FOR STABILISING POLYMERISABLE COMPOUNDS BASF SE (DE) 2015-10-28 EP claimed
US-20140228571-A1 METHOD OF STABILIZING POLYMERIZABLE COMPOUNDS BASF SE (DE) 2014-08-14 US claimed
WO-2014095437-A2 METHOD FOR STABILISING POLYMERISABLE COMPOUNDS BASF SE (DE) 2014-06-26 WO claimed
EP-0649425-B1 PYRIDINO-, PYRROLIDINO- AND AZEPINO-SUBSTITUTED OXIMES USEFUL AS ANTI-ATHEROSCLEROSIS AND ANTI-HYPERCHOLESTEROLEMIC AGENTS UPJOHN CO (US) 1999-03-10 EP claimed
US-5597816-A Pyrazoloazepino substituted oximes useful as anti-atherosclerosis and anti-hypercholesterolemic agents THE UPJOHN COMPANY (US) 1997-01-28 US claimed
EP-0271798-B1 O-SUBSTITUTED TETRAHYDROPYRIDINE OXIME CHOLINERGIC AGENTS WARNER-LAMBERT COMPANY (US) 1993-04-07 EP claimed
EP-0368866-A1 ARYL SUBSTITUTED NAPHTHALENE, BENZOXEPINE, BENZAZEPINE, BENZOCYCLOHEPTENE DERIVATIVES SCHERING CORPORATION (US) 1990-05-23 EP claimed
WO-1988008836-A2 ARYL SUBSTITUTED NAPHTHALENE, BENZOXEPINE, BENZAZEPINE, BENZOCYCLOHEPTENE DERIVATIVES SCHERING CORPORATION (US) 1988-11-17 WO claimed
EP-0145506-B1 ELIMINATION OF DEFECTS IN CYSTEINE-SENSITIZED EMULSIONS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1988-03-02 EP claimed
US-4710508-A ANALGESICS WARNER-LAMBERT COMPANY (US) 1987-12-01 US claimed
EP-0145506-A2 Elimination of defects in cysteine-sensitized emulsions E.I. DU PONT DE NEMOURS AND COMPANY (US) 1985-06-19 EP claimed
US-4514492-A Elimination of defects in cysteine-sensitized emulsions E. I. DU PONT DE NEMOURS AND COMPANY (US) 1985-04-30 US claimed
US-4225679-A Floral foam product and method of producing the same which incorporates a flower preservative and a bacteriocide PENNOCK, VILLAMIL AND PILATO INC. (US) 1980-09-30 US 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-20140228571-A1 METHOD OF STABILIZING POLYMERIZABLE COMPOUNDS AOC1, AOC2, AOC3 LMNA 545/4885METAP2 3354/4885METAP1 4099/4885

“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.