SCHEMBL4918988

SCHEMBL4918988

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

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TDP1 Q9NUW8 5/20 0.52
▸ ALDH1A1 P00352 4/20 0.52
▸ TSHR P16473 7/20 0.45
▸ GRIN2D O15399 1/20 0.44
▸ GRIN3B O60391 1/20 0.44
▸ GRIN1 Q05586 1/20 0.44
▸ GRIN2A Q12879 1/20 0.44
▸ GRIN2B Q13224 1/20 0.44
▸ GRIN2C Q14957 1/20 0.44
▸ GRIN3A Q8TCU5 1/20 0.44
▸ CYP1A2 P05177 1/20 0.43
▸ MEN1 O00255 1/20 0.43
▸ KMT2A Q03164 1/20 0.43
▸ SMN1; SMN2 Q16637 1/20 0.41
▸ TRPM8 Q7Z2W7 1/20 0.41
▸ LMNA P02545 1/20 0.41
▸ GAA P10253 1/20 0.41
▸ MAPT P10636 1/20 0.41
▸ L3MBTL1 Q9Y468 1/20 0.41
▸ CYP3A4 P08684 1/20 0.40

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
SCHEMBL14020980 0.90 ALDH1A1 (0.48) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL28420852 0.86 ALDH1A1 (0.54) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL7527476 0.86 CYP1A2 (0.52) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL2581020 0.85 GRIN2D (0.50) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL23214259 0.84 TSHR (0.48) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL31329961 0.84 CYP1A2 (0.50) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL29796101 0.84 TSHR (0.48) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL3981776 0.84 CYP1A2 (0.50) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL6579700 0.84 ALDH1A1 (0.54) TDP1ALDH1A1TSHRGRIN2DGRIN3B
SCHEMBL6580997 0.84 ALDH1A1 (0.47) TDP1ALDH1A1TSHRGRIN2DGRIN3B

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 49 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105254510-B The synthetic method of 2,4,6-trimethyl m-phenylenediamine 江苏天嘉宜化工有限公司 2018-07-13 — — CN claimed
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
EP-1232748-A1 SUBSTITUTED NITROBENZENE DERIVATIVES AS MEDICINES AND OTHER USEFUL USES THEREOF Men, Tewa (CN) 2002-08-21 — — EP claimed
WO-1995020637-A2 HYDROCARBON OIL-AQUEOUS FUEL AND ADDITIVE COMPOSITIONS MEG S.N.C. DI SCOPELLITI SOFIA & C. (IT) 1995-08-03 — — WO claimed
CN-114292155-B Method for purifying mesitylene through thermal coupling 黄河三角洲京博化工研究院有限公司 2024-05-03 — — CN disclosed
CN-114213208-B Method for extracting, rectifying and purifying mesitylene by high-efficiency composite solvent 黄河三角洲京博化工研究院有限公司 2024-01-30 — — CN disclosed
CN-114292155-A Method for thermally coupling and purifying mesitylene 黄河三角洲京博化工研究院有限公司 2022-04-08 — — CN disclosed
CN-114213208-A Method for extracting, rectifying and purifying mesitylene by using efficient composite solvent 黄河三角洲京博化工研究院有限公司 2022-03-22 — — CN disclosed
CN-113354543-A Novel environment-friendly production process for preparing amino product and H-acid by silane chemical reduction of nitro compounds 深圳有为技术控股集团有限公司 2021-09-07 — — CN disclosed
US-10408850-B1 Method for target substance detection and measurement HOUND LABS, INC. (US) 2019-09-10 — — US disclosed
CN-109311889-A Activin receptor-like kinase inhibitors 蓝图药品公司 2019-02-05 — — CN disclosed
US-4170708-A FROM AN AROMATIC NITRO COMPOUND, AN ALCOHOL, AND CARBON MONOXIDE MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1979-10-09 — — US disclosed
EP-0000563-A1 Process for preparing aromatic urethanes MITSUI TOATSU CHEMICALS, Inc. (JP) 1979-02-07 — — EP disclosed
US-4134880-A Process for producing an aromatic urethane from nitro compounds, hydroxyl compounds and carbon monoxide using metal-Lewis acid-ammonia catalyst systems MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1979-01-16 — — US disclosed
US-4080365-A Process for preparing aromatic urethanes MITSUI TOATSU CHEMICALS (JA) 1978-03-21 — — US disclosed
US-4070391-A Process for producing isocyanate from nitro compounds and carbon monoxide using rhodium oxide catalysts ETHYL CORPORATION (US) 1978-01-24 — — US disclosed
US-4052420-A PROCESS FOR PRODUCING DIURETHANE FROM DINITRO COMPOUNDS, HYDROXYL COMPOUNDS AND CARBON MONOXIDE ETHYL CORPORATION (US) 1977-10-04 — — US disclosed
US-4052437-A PROCESS FOR PRODUCING URETHANE FROM NITRO COMPOUNDS, HYDROXYL COMPOUNDS AND CARBON MONOXIDE USING RHODIUM OXIDE CATALYSTS ETHYL CORPORATION (US) 1977-10-04 — — US 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 (3 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 TDP1 1154/4885ALDH1A1 571/4885TSHR 3651/4885
US-20050228055-A1 Substituted nitrobenzene derivatives as pharmaceutical and other uses athereof APOB, NDUFB1, CYP2F1 TDP1 1548/4885ALDH1A1 700/4885TSHR 4369/4885
US-10408850-B1 Method for target substance detection and measurement CNR1, CNR2, ALK TDP1 4700/4885ALDH1A1 321/4885TSHR 2771/4885

“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.

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