SCHEMBL6230239

SCHEMBL6230239

Cc1ccc(NC(=O)c2cnoc2C)cc1

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 9/20 0.72
NPC1 O15118 7/20 0.72
SMN1; SMN2 Q16637 4/20 0.72
TP53 P04637 3/20 0.72
HTT P42858 3/20 0.72
LMNA P02545 3/20 0.72
DHODH Q02127 2/20 0.72
GMNN O75496 1/20 0.72
CYP1A2 P05177 1/20 0.72
CYP3A4 P08684 1/20 0.72
HTR1A P08908 1/20 0.72
THRB P10828 1/20 0.72
PIM1 P11309 1/20 0.72
CYP2C9 P11712 1/20 0.72
MAOA P21397 1/20 0.72
SLC6A2 P23975 1/20 0.72
HTR2A P28223 1/20 0.72
AGTR1 P30556 1/20 0.72
CCKBR P32239 1/20 0.72
MC4R P32245 1/20 0.72

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
SCHEMBL8812469 0.93 RAB9A (0.64) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL8812360 0.89 RAB9A (0.70) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL11441650 0.88 RAB9A (0.72) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL20456411 0.88 RAB9A (0.68) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL6415832 0.87 RAB9A (0.72) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL8813278 0.85 RAB9A (0.65) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL15711547 0.85 RAB9A (0.65) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL9812368 0.85 RAB9A (0.78) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL7558642 0.85 RAB9A (0.65) RAB9ANPC1SMN1; SMN2TP53HTT
SCHEMBL8813186 0.84 DHODH (0.71) RAB9ANPC1SMN1; SMN2TP53HTT

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040127532-A1 Method for synthesizing leflunomide AVRUTOV ILYA (IL) 2004-07-01 US claimed
US-6723855-B2 CHLORINATING 5-METHYLISOXAZOLE-4-CARBOXYLIC ACID BY REACTING WITH CHLORINATING AGENT TO FORM 5-METHYLISOXAZOLE-4-CARBOXYLIC ACID CHLORIDE, REACTING WITH 4-TRIFLUOROMETHYLANILINE IN PRESENCE OF ALKALI METAL OR ALKALINE EARTH METAL BICARBONATE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-04-20 US claimed
JP-2004500380-A 2004-01-08 JP claimed
EP-1257270-A4 A METHOD FOR SYNTHESIZING LEFLUNOMIDE TEVA PHARMA (IL) 2003-05-07 EP claimed
EP-1257270-A1 A METHOD FOR SYNTHESIZING LEFLUNOMIDE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2002-11-20 EP claimed
US-20020022646-A1 Method for systhesizing leflunomide TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2002-02-21 US claimed
WO-2001060363-A1 A METHOD FOR SYNTHESIZING LEFLUNOMIDE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2001-08-23 WO claimed
EP-3786164-A1 METHODS AND COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF HEARING LOSS Ting Therapeutics LLC (US) 2021-03-03 EP disclosed
US-10881666-B2 Combination pharmaceutical agents as RSV inhibitors ENANTA PHARMACEUTICALS, INC. (US) 2021-01-05 US disclosed
US-20190192535-A1 COMBINATION PHARMACEUTICAL AGENTS AS RSV INHIBITORS ENANTA PHARMACEUTICALS, INC. 2019-06-27 US disclosed
US-20180161340-A1 METHODS AND COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF HEARING LOSS ST. JUDE CHILDREN'S RESEARCH HOSPITAL 2018-06-14 US disclosed
US-20100022467-A1 ANTI-CANCER PHOSPHONATE ANALOGS BOOJAMRA CONSTANTINE G 2010-01-28 US disclosed
EP-1257270-B1 A METHOD FOR SYNTHESIZING LEFLUNOMIDE TEVA PHARMA (IL) 2005-04-13 EP disclosed
EP-1473035-A1 Leflunomide of high purity TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-11-03 EP disclosed
EP-1473035-A1 Leflunomide of high purity TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-11-03 EP disclosed
US-20040127532-A1 Method for synthesizing leflunomide AVRUTOV ILYA (IL) 2004-07-01 US disclosed
EP-1257270-A4 A METHOD FOR SYNTHESIZING LEFLUNOMIDE TEVA PHARMA (IL) 2003-05-07 EP disclosed
EP-1257270-A1 A METHOD FOR SYNTHESIZING LEFLUNOMIDE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2002-11-20 EP disclosed
US-20020022646-A1 Method for systhesizing leflunomide TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2002-02-21 US disclosed
WO-2001060363-A1 A METHOD FOR SYNTHESIZING LEFLUNOMIDE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2001-08-23 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 (6 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-10881666-B2 Combination pharmaceutical agents as RSV inhibitors SERPINB1, FURIN, HIF1AN RAB9A 704/4885NPC1 480/4885SMN1; SMN2 709/4885
US-20020022646-A1 Method for systhesizing leflunomide FAH, LEF1, HMGCR RAB9A 2074/4885NPC1 1244/4885SMN1; SMN2 570/4885
US-20180161340-A1 METHODS AND COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF HEARING LOSS CDK2, CDK5, CDK20 RAB9A 4509/4885NPC1 1827/4885SMN1; SMN2 2538/4885
US-20040127532-A1 Method for synthesizing leflunomide LEF1, CYP3A5, CYP2F1 RAB9A 2319/4885NPC1 956/4885SMN1; SMN2 1333/4885
US-20100022467-A1 ANTI-CANCER PHOSPHONATE ANALOGS PIK3CA, PHOSPHO1, PTEN RAB9A 1324/4885NPC1 1815/4885SMN1; SMN2 3947/4885
US-20190192535-A1 COMBINATION PHARMACEUTICAL AGENTS AS RSV INHIBITORS SERPINB1, FURIN, HIF1AN RAB9A 704/4885NPC1 480/4885SMN1; SMN2 709/4885

“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.