SCHEMBL7086751

SCHEMBL7086751

O=[N+]([O-])c1ccccc1N=Nc1ccc[c]c1O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN11 Q06124 5/20 0.50
PLAU P00749 1/20 0.49
NPC1 O15118 2/20 0.48
RAB9A P51151 2/20 0.48
CCNT1 O60563 1/20 0.45
CCNB2 O95067 1/20 0.45
CCNE2 O96020 1/20 0.45
CDK1 P06493 1/20 0.45
CDK4 P11802 1/20 0.45
CCNB1 P14635 1/20 0.45
CCNA2 P20248 1/20 0.45
CCND1 P24385 1/20 0.45
CCNE1 P24864 1/20 0.45
CDK2 P24941 1/20 0.45
CDK7 P50613 1/20 0.45
CDK9 P50750 1/20 0.45
CCNH P51946 1/20 0.45
CCNA1 P78396 1/20 0.45
CCNB3 Q8WWL7 1/20 0.45
SMN1; SMN2 Q16637 2/20 0.43

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
SCHEMBL7086750 0.84 PTPN11 (0.50) PTPN11PLAUNPC1RAB9ACCNT1
SCHEMBL41322 0.79 GPR35 (0.54) PLAUSMN1; SMN2GPR35MEN1KMT2A
SCHEMBL7538891 0.79 PLAU (0.46) PTPN11PLAUNPC1RAB9ACCNT1
SCHEMBL5838349 0.78 NPC1 (0.59) PTPN11PLAUNPC1RAB9ACCNT1
SCHEMBL5838346 0.78 NPC1 (0.59) PTPN11PLAUNPC1RAB9ACCNT1
SCHEMBL24213305 0.78 NPC1 (0.59) PTPN11PLAUNPC1RAB9ACCNT1
SCHEMBL11217415 0.78 IDE (0.53) PTPN11PLAUNPC1RAB9ACCNT1
SCHEMBL1263553 0.76 PLAU (0.53) PTPN11PLAUNPC1RAB9ACCNT1
SCHEMBL1263552 0.76 PLAU (0.53) PTPN11PLAUNPC1RAB9ACCNT1
Charcoal, Activated SCHEMBL5133893 0.75 PLAU (0.51) PTPN11PLAUNPC1RAB9ACCNT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2134370-A None JP disclosed
EP-1351944-A1 METHOD FOR PREPARING 2-(2-HYDROXYPHENYL)-2H-BENZOTRIAZOLE LG Chem Ltd. (KR) 2003-10-15 EP disclosed
US-6559316-B2 Reacting o-nitrophenylazohydroxyphenyl compound with hydrazine hydrate; reduction in presence of water, zinc powder, and sulfuric acid with/without phase transfer catalyst LG CHEM, LTD. (KR) 2003-05-06 US disclosed
US-20030050480-A1 METHOD FOR PREPARING 2-(2-HYRDROXYPHENYL)-2H-BENZOTRIAZOLE LG CHEM, LTD. (KR) 2003-03-13 US disclosed
WO-2002055508-A1 METHOD FOR PREPARING 2-(2-HYDROXYPHENYL)-2H-BENZOTRIAZOLE LG CHEM, LTD. (KR) 2002-07-18 WO disclosed
US-5571924-A Process for the preparation of benzotriazoles CIBA-GEIGY CORPORATION (US) 1996-11-05 US disclosed
US-5276161-A Catalytic hydrogenation of o-nitrophenylazohydroxyphenyl compounds; noble metal catalyst and organic amine CIBA-GEIGY CORPORATION (US) 1994-01-04 US disclosed
US-4999433-A Process for the preparation of benzotriazole derivatives CIBA-GEIGY CORPORATION (US) 1991-03-12 US disclosed
JP-H02134370-A PRODUCTION OF BENZOTRIAZOLE DERIVATIVE CIBA GEIGY AG 1990-05-23 JP 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 (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-20030050480-A1 METHOD FOR PREPARING 2-(2-HYRDROXYPHENYL)-2H-BENZOTRIAZOLE CYP8B1, CYP4Z1, CBR1 PTPN11 2902/4885PLAU 3762/4885NPC1 1433/4885

“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.