SCHEMBL4913846

SCHEMBL4913846

Cc1cc(C)c([N+](=O)[O-])c(C(C)(C)C)c1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 5/20 0.47
ALDH1A1 P00352 4/20 0.47
TDP1 Q9NUW8 3/20 0.47
SMN1; SMN2 Q16637 3/20 0.44
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
GALR3 O60755 1/20 0.44
HTT P42858 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
CA2 P00918 1/20 0.43
POLB P06746 1/20 0.43
TYR P14679 1/20 0.43
GRIN2D O15399 1/20 0.41
GRIN3B O60391 1/20 0.41
GRIN1 Q05586 1/20 0.41
GRIN2A Q12879 1/20 0.41
GRIN2B Q13224 1/20 0.41
GRIN2C Q14957 1/20 0.41
GRIN3A Q8TCU5 1/20 0.41
GPR35 Q9HC97 1/20 0.39

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
SCHEMBL12191080 0.85 TSHR (0.41) TSHRALDH1A1TDP1MEN1KMT2A
SCHEMBL1820951 0.83 ALDH1A1 (0.58) TSHRALDH1A1TDP1MEN1KMT2A
SCHEMBL28308139 0.82 TSHR (0.49) TSHRALDH1A1TDP1SMN1; SMN2MEN1
SCHEMBL4923093 0.80 TSHR (0.51) TSHRALDH1A1TDP1SMN1; SMN2MEN1
SCHEMBL10813783 0.79 TSHR (0.54) TSHRALDH1A1TDP1SMN1; SMN2MEN1
SCHEMBL2230167 0.77 TDP1 (0.52) TSHRALDH1A1TDP1SMN1; SMN2MEN1
SCHEMBL10411480 0.76 SMN1; SMN2 (0.58) TSHRALDH1A1TDP1SMN1; SMN2MEN1
SCHEMBL4924664 0.75 SMN1; SMN2 (0.47) TSHRALDH1A1TDP1SMN1; SMN2MEN1
SCHEMBL9719276 0.75 GPR35 (0.57) TSHRALDH1A1TDP1SMN1; SMN2L3MBTL1
SCHEMBL4924130 0.75 ALDH1A1 (0.45) TSHRALDH1A1TDP1SMN1; SMN2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080227869-A1 Substituted nitrobenzene derivatives as pharmaceutical and other uses thereof MEN TEWA 2008-09-18 US claimed
EP-1232748-B1 USE OF SUBSTITUTED NITROBENZENE DERIVATIVES FOR THE TREATMENT OF DISEASES CAUSED BY BACTERIA, FUNGI AND VIRUSES MEN TEWA (CN) 2006-05-03 EP claimed
US-20050228055-A1 Substituted nitrobenzene derivatives as pharmaceutical and other uses athereof MEN TEWA 2005-10-13 US claimed
CN-1679521-A Use of substituting nitrobenzene derivative in products preparation MEN TEWA (CN) 2005-10-12 CN claimed
CN-1193746-C Substituted nitrobenzene derivatives as pharmaceutical and other beneficial uses NEN TEWA (CN) 2005-03-23 CN claimed
EP-1232748-A1 SUBSTITUTED NITROBENZENE DERIVATIVES AS MEDICINES AND OTHER USEFUL USES THEREOF Men, Tewa (CN) 2002-08-21 EP claimed
CN-1294911-A Substituted nitrobenzene derivatives as pharmaceutical and other beneficial uses MEN TEWA (CN) 2001-05-16 CN claimed
US-20080227869-A1 Substituted nitrobenzene derivatives as pharmaceutical and other uses thereof MEN TEWA 2008-09-18 US disclosed
EP-1232748-B1 USE OF SUBSTITUTED NITROBENZENE DERIVATIVES FOR THE TREATMENT OF DISEASES CAUSED BY BACTERIA, FUNGI AND VIRUSES MEN TEWA (CN) 2006-05-03 EP disclosed
US-20050228055-A1 Substituted nitrobenzene derivatives as pharmaceutical and other uses athereof MEN TEWA 2005-10-13 US disclosed
CN-1679521-A Use of substituting nitrobenzene derivative in products preparation MEN TEWA (CN) 2005-10-12 CN disclosed
CN-1193746-C Substituted nitrobenzene derivatives as pharmaceutical and other beneficial uses NEN TEWA (CN) 2005-03-23 CN disclosed
EP-1232748-A1 SUBSTITUTED NITROBENZENE DERIVATIVES AS MEDICINES AND OTHER USEFUL USES THEREOF Men, Tewa (CN) 2002-08-21 EP disclosed
CN-1294911-A Substituted nitrobenzene derivatives as pharmaceutical and other beneficial uses MEN TEWA (CN) 2001-05-16 CN disclosed
CN-1049124-C Artificial musk serial anti-inflammatory and anticancer compound Chinese patent medicine and making process thereof BEIFANG MEDICINE DEVEL INST ZU (CN) 2000-02-09 CN disclosed
EP-0497989-B1 POLLUTION-FREE PROCESS FOR PRODUCING AROMATIC NITRO COMPOUND WITHOUT USING MINERAL ACID NIPPON KAYAKU KK (JP) 1995-10-18 EP disclosed
EP-0497989-A1 POLLUTION-FREE PROCESS FOR PRODUCING AROMATIC NITRO COMPOUND WITHOUT USING MINERAL ACID NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1992-08-12 EP 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 (2 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-20080227869-A1 Substituted nitrobenzene derivatives as pharmaceutical and other uses thereof NOS3, NOS1, PTGS1 TSHR 3651/4885ALDH1A1 571/4885TDP1 1154/4885
US-20050228055-A1 Substituted nitrobenzene derivatives as pharmaceutical and other uses athereof APOB, NDUFB1, CYP2F1 TSHR 4369/4885ALDH1A1 700/4885TDP1 1548/4885

“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.