SCHEMBL6312816

SCHEMBL6312816

O=[N+]([O-])c1cc2ccccc2nc1-c1ccccc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 7/20 0.60
MEN1 O00255 5/20 0.60
PDE10A Q9Y233 1/20 0.53
RAB9A P51151 3/20 0.51
ALDH1A1 P00352 3/20 0.46
CRHBP P24387 1/20 0.45
CRHR2 Q13324 1/20 0.45
CYP1A2 P05177 1/20 0.44
OPRK1 P41145 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
KDM4E B2RXH2 1/20 0.44
PKM P14618 1/20 0.44
MAOA P21397 1/20 0.44
HTT P42858 1/20 0.43
ATM Q13315 1/20 0.43
CASP6 P55212 1/20 0.42
NPC1 O15118 1/20 0.42
ABCG2 Q9UNQ0 1/20 0.42
MAPT P10636 2/20 0.41
MAPK1 P28482 1/20 0.41

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
Quinoline SCHEMBL28250429 0.90 KMT2A (0.51) KMT2AMEN1PDE10ARAB9AALDH1A1
SCHEMBL28505934 0.83 KMT2A (0.50) KMT2AMEN1ALDH1A1CRHBPCRHR2
SCHEMBL28241457 0.78 MEN1 (0.47) KMT2AMEN1RAB9AALDH1A1CYP1A2
SCHEMBL28242021 0.78 L3MBTL1 (0.52) KMT2AMEN1ALDH1A1TDP1KDM4E
SCHEMBL9120430 0.77 RAB9A (0.55) KMT2AMEN1RAB9AALDH1A1CYP1A2
SCHEMBL1682777 0.77 RAB9A (0.55) KMT2AMEN1PDE10ARAB9AALDH1A1
SCHEMBL11414775 0.77 MEN1 (0.54) KMT2AMEN1RAB9AALDH1A1TDP1
Acridine SCHEMBL27545385 0.77 RAB9A (0.63) KMT2AMEN1PDE10ARAB9AALDH1A1
SCHEMBL11108095 0.76 RAB9A (0.54) KMT2AMEN1PDE10ARAB9AALDH1A1
SCHEMBL2011678 0.76 RAB9A (0.54) KMT2AMEN1RAB9AALDH1A1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108558751-B Synthesis process of 3-nitroquinoline derivative 武汉工程大学 2021-01-05 CN disclosed
CN-108558750-B Process for synthesizing 3-nitroquinoline derivative by solvent-free method 武汉工程大学 2021-01-05 CN disclosed
CN-108558878-B Synthesis process of quinoline and derivatives thereof 武汉工程大学 2020-10-23 CN disclosed
CN-108558750-A The technique that solventless method synthesizes 3- nitroquinoline derivatives 武汉工程大学 2018-09-21 CN disclosed
CN-108558878-A A kind of synthesis technology of quindoline and its derivative 武汉工程大学 2018-09-21 CN disclosed
CN-108558751-A The synthesis technology of 3- nitroquinoline derivatives 武汉工程大学 2018-09-21 CN disclosed
US-6939874-B2 Substituted pyrimidinyl derivatives and methods of use AMGEN INC. (US) 2005-09-06 US disclosed
EP-1427421-A1 2,4-DISUBSTITUTED PYRIMIDINYL DERIVATIVES FOR USE AS ANTICANCER AGENTS Amgen Inc. (US) 2004-06-16 EP disclosed
US-20040063705-A1 Substituted pyrimidinyl derivatives and methods of use AMGEN INC. 2004-04-01 US disclosed
WO-2003018021-A1 2,4-DISUBSTITUTED PYRIMIDINYL DERIVATIVES FOR USE AS ANTICANCER AGENTS AMGEN INC. (US) 2003-03-06 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 (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-20040063705-A1 Substituted pyrimidinyl derivatives and methods of use DPYD, TYMP, TPMT KMT2A 2974/4885MEN1 1164/4885PDE10A 1001/4885

“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.