SCHEMBL2706463

SCHEMBL2706463

O=C(OCc1ccccc1)c1ccccc1[N+](=O)[O-]

nearest known ligand 0.63

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.61
TDP1 Q9NUW8 3/20 0.59
L3MBTL1 Q9Y468 2/20 0.58
RAB9A P51151 3/20 0.58
NPC1 O15118 2/20 0.53
KMT2A Q03164 4/20 0.53
SLC6A2 P23975 1/20 0.53
SLC6A3 Q01959 1/20 0.53
CYP3A4 P08684 1/20 0.52
TSHR P16473 1/20 0.52
MAPK1 P28482 1/20 0.52
HTT P42858 3/20 0.52
LMNA P02545 3/20 0.52
MAPT P10636 1/20 0.52
POLB P06746 3/20 0.52
MEN1 O00255 2/20 0.52
CTSD P07339 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.48

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
SCHEMBL19451176 0.88 ALDH1A1 (0.55) ALDH1A1TDP1L3MBTL1RAB9AKMT2A
SCHEMBL12569605 0.87 ALDH1A1 (0.54) ALDH1A1TDP1L3MBTL1RAB9AKMT2A
SCHEMBL2014208 0.87 TSHR (0.60) ALDH1A1TDP1L3MBTL1RAB9ANPC1
SCHEMBL2005800 0.87 RAB9A (0.59) ALDH1A1TDP1L3MBTL1RAB9ANPC1
SCHEMBL6276517 0.86 ALDH1A1 (0.52) ALDH1A1TDP1L3MBTL1RAB9AKMT2A
SCHEMBL7886556 0.85 TDP1 (0.54) ALDH1A1TDP1L3MBTL1RAB9AKMT2A
SCHEMBL2009221 0.85 ALDH1A1 (0.51) ALDH1A1TDP1L3MBTL1RAB9AKMT2A
SCHEMBL5663592 0.85 L3MBTL1 (0.51) ALDH1A1TDP1L3MBTL1RAB9ANPC1
SCHEMBL2704301 0.85 ALDH1A1 (0.51) ALDH1A1TDP1L3MBTL1RAB9ANPC1
SCHEMBL29172358 0.85 L3MBTL1 (0.62) ALDH1A1TDP1L3MBTL1RAB9ANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110204490-B Preparation method of disubstituted 4-chloroquinoline-3-carbonitrile derivative and bosutinib 新发药业有限公司 2021-01-01 CN disclosed
EP-2609067-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ESTER Sumitomo Chemical Co., Ltd (JP) 2013-07-03 EP disclosed
US-20130150611-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ESTER SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2013-06-13 US disclosed
WO-2012176930-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ESTER SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-12-27 WO disclosed
WO-2012026617-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ESTER SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-03-01 WO disclosed
CN-1110484-C 2-(arylphenyl) amino-imidazoline derivatives HOFMMANN LA ROCHE AG F (CH) 2003-06-04 CN disclosed
CN-1216762-A 2-(arylphenyl) amino-imidazoline derivatives HOFMMANN LA ROCHE AG F (CH) 1999-05-19 CN 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-20130150611-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ESTER ADH5, ADH1A, ADH1C ALDH1A1 33/4885TDP1 4303/4885L3MBTL1 2107/4885

“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.