SCHEMBL29348

SCHEMBL29348

O=[N+]([O-])c1ccc(Cl)cc1F

nearest known ligand 0.64

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 3/20 0.64
TDP1 Q9NUW8 2/20 0.64
TSHR P16473 1/20 0.64
ATM Q13315 1/20 0.64
ALDH1A1 P00352 4/20 0.53
POLB P06746 2/20 0.53
MAPT P10636 1/20 0.53
HIF1A Q16665 1/20 0.52
PDE7A Q13946 5/20 0.50
VCAM1 P19320 2/20 0.50
LMNA P02545 1/20 0.50
PDE7B Q9NP56 2/20 0.46
PDE4B Q07343 1/20 0.46
PDE4D Q08499 1/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
MEN1 O00255 1/20 0.45
KMT2A Q03164 1/20 0.45

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
SCHEMBL29485896 1.00 MAPK1 (0.64) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL5804418 0.93 TSHR (0.79) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL10531067 0.93 MAPK1 (0.56) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL306375 0.85 ALDH1A1 (0.64) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL29580152 0.85 ALDH1A1 (0.64) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL2655681 0.85 TDP1 (0.56) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL1524058 0.80 MAPK1 (0.72) MAPK1TDP1TSHRALDH1A1POLB
SCHEMBL18547550 0.79 VCAM1 (0.57) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL27542809 0.79 VCAM1 (0.62) MAPK1TDP1TSHRATMALDH1A1
SCHEMBL11516745 0.78 MAPK1 (0.69) MAPK1TDP1TSHRALDH1A1POLB

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 1031 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106117067-B A kind of method that diazotising prepares 3,5 difluoro, 4 chloronitrobenzene 江苏扬农化工集团有限公司 2018-04-20 CN claimed
CN-106905161-A A kind of synthetic method of the nitrobenzoic acid of 2 chlorine, 4 fluorine 5 常州沃腾化工科技有限公司 2017-06-30 CN claimed
CN-1162393-C Chemical synthesis process of 4-chloro-2-fluoro nitrobenzene 浙江工业大学 2004-08-18 CN claimed
CN-1398846-A Chemical synthesis process of 4-chloro-2-fluoro nitrobenzene UNIV ZHEJIANG POLYTECHNIC (CN) 2003-02-26 CN claimed
JP-3109360-A None JP disclosed
US-20260048035-A1 MODULATORS OF TNF-ALPHA ACTIVITY FORWARD THERAPEUTICS INC (US) 2026-02-19 US disclosed
US-20260028348-A1 MODULATORS OF TNF-ALPHA ACTIVITY FORWARD THERAPEUTICS INC (US) 2026-01-29 US disclosed
EP-3976604-B1 1,3,4-OXADIAZOLE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME CHONG KUN DANG PHARMACEUTICAL CORP (KR) 2026-01-21 EP disclosed
US-12521368-B2 Modulators of TNF-alpha activity FORWARD THERAPEUTICS, INC. (US) 2026-01-13 US disclosed
EP-4663630-A1 NOVEL BENZIMIDAZOLONE DERIVATIVE COMPOUND AS AUTOTAXIN INHIBITOR LG Chem, Ltd. (KR) 2025-12-17 EP disclosed
US-12473263-B2 Bicyclic inhibitors of CBX chromodomains ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2025-11-18 US disclosed
US-20250345310-A1 MODULATORS OF TNF-ALPHA ACTIVITY FORWARD THERAPEUTICS INC (US) 2025-11-13 US disclosed
US-4229365-A Manufacture of substituted fluorobenzenes BASF AKTIENGESELLSCHAFT (DE) 1980-10-21 US disclosed
US-4226811-A Preparation of substituted fluorobenzenes BASF AKTIENGESELLSCHAFT (DE) 1980-10-07 US disclosed
US-4224340-A Anti-inflammatory compositions containing α-phenyl-N-phenylnitrone compounds WILLIAM H. RORER, INC. (US) 1980-09-23 US disclosed
US-4214003-A ANTIINFLAMMATORY AGENTS WILLIAM H. RORER, INC. (US) 1980-07-22 US disclosed
US-4197314-A WITH A DIPHENYL NITRONE WILLIAM H. RORER, INC. (US) 1980-04-08 US disclosed
US-4164517-A REACTING A CHLORONITROBENZENE WITH POTASSIUM FLUORIDE IN SULFOLANE I.S.C. CHEMICALS LIMITED (GB) 1979-08-14 US disclosed
EP-0003344-A1 Process for the preparation of fluor benzenes BASF Aktiengesellschaft (DE) 1979-08-08 EP disclosed
US-4153722-A ANTIINFLAMMATORY, A-PHENYL-N-PHENYLNITRONE WILLIAM H. RORER, INC. (US) 1979-05-08 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 (4 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-12473263-B2 Bicyclic inhibitors of CBX chromodomains CBX2, CBX3, CBX6 MAPK1 2699/4885TDP1 2682/4885TSHR 4302/4885
US-20260028348-A1 MODULATORS OF TNF-ALPHA ACTIVITY TNF, TNFRSF1A, TNFRSF9 MAPK1 729/4885TDP1 4065/4885TSHR 396/4885
US-20260048035-A1 MODULATORS OF TNF-ALPHA ACTIVITY TNF, TNFRSF1A, CD40 MAPK1 744/4885TDP1 501/4885TSHR 1074/4885
US-20250345310-A1 MODULATORS OF TNF-ALPHA ACTIVITY TNF, TNFRSF1A, NFKBIA MAPK1 1136/4885TDP1 1565/4885TSHR 2727/4885

“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.