SCHEMBL2481319

SCHEMBL2481319

Cc1c([N+](=O)[O-])ccc(F)c1F

nearest known ligand 0.54

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 3/20 0.54
TSHR P16473 9/20 0.48
SMN1; SMN2 Q16637 3/20 0.48
ATM Q13315 1/20 0.48
ALDH1A1 P00352 2/20 0.47
HIF1A Q16665 2/20 0.47
CYP3A4 P08684 3/20 0.45
MAPT P10636 2/20 0.44
KDM4E B2RXH2 1/20 0.44
LMNA P02545 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
VCAM1 P19320 1/20 0.44
CASP6 P55212 1/20 0.43
HSD17B10 Q99714 1/20 0.42
MAPK1 P28482 1/20 0.39
TP53 P04637 1/20 0.37
HPGD P15428 1/20 0.37
CYP1A2 P05177 1/20 0.37
RECQL P46063 1/20 0.37

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
SCHEMBL29902915 1.00 TDP1 (0.54) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL1636077 0.89 TDP1 (0.60) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL1424697 0.85 TDP1 (0.56) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL29888274 0.85 TDP1 (0.50) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL29788829 0.85 TDP1 (0.56) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL574038 0.85 TDP1 (0.50) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL27843138 0.84 TSHR (0.50) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL14411817 0.83 TDP1 (0.54) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL7327212 0.82 TDP1 (0.41) TDP1TSHRSMN1; SMN2ATMALDH1A1
SCHEMBL397110 0.82 TDP1 (0.52) TDP1TSHRSMN1; SMN2ATMALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117049938-B Preparation method of 6-bromo-2, 3-difluorotoluene 山东轩德医药科技有限公司 2024-06-14 CN claimed
CN-117049938-A Preparation method of 6-bromo-2, 3-difluorotoluene 山东轩德医药科技有限公司 2023-11-14 CN claimed
WO-2026087442-A1 AMINO-IMIDAZOLE ANTIBACTERIAL COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2026-04-30 WO disclosed
EP-3590516-B1 ANTITUMOR-EFFECT ENHANCER USING PYRAZOLO[3,4-D]PYRIMIDINE COMPOUND TAIHO PHARMACEUTICAL CO LTD (JP) 2025-09-03 EP disclosed
CN-117049938-B Preparation method of 6-bromo-2, 3-difluorotoluene 山东轩德医药科技有限公司 2024-06-14 CN disclosed
CN-117049938-B Preparation method of 6-bromo-2, 3-difluorotoluene 山东轩德医药科技有限公司 2024-06-14 CN disclosed
US-20240116921-A1 LACTAM (HETERO)ARYLFUSEDPYRIMIDINE DERIVATIVES AS INHIBITORS OF ERBB2 ENLIVEN INC. 2024-04-11 US disclosed
CN-115232144-B Nitrogen-containing condensed ring derivative, pharmaceutical composition, and preparation method and application thereof 长春金赛药业有限责任公司 2024-04-02 CN disclosed
CN-117049938-A Preparation method of 6-bromo-2, 3-difluorotoluene 山东轩德医药科技有限公司 2023-11-14 CN disclosed
CN-117049938-A Preparation method of 6-bromo-2, 3-difluorotoluene 山东轩德医药科技有限公司 2023-11-14 CN disclosed
EP-4267137-A1 LACTAM (HETERO)ARYLFUSEDPYRIMIDINE DERIVATIVES AS INHIBITORS OF ERBB2 Enliven Inc. (US) 2023-11-01 EP disclosed
WO-2010066684-A2 Pyridyloxyindoles Inhibitors of VEGF-R2 and Use Thereof for Treatment of Disease NOVARTIS AG (CH) 2010-06-17 WO disclosed
US-20080255195-A1 Compounds Which Have Activity at M1 Receptor and Their Uses in Medicine GLAXO GROUP LIMITED (GB) 2008-10-16 US disclosed
EP-1943230-A2 COMPOUNDS WHICH HAVE ACTIVITY AT M1 RECEPTOR AND THEIR USES IN MEDICINE GLAXO GROUP LIMITED (GB) 2008-07-16 EP disclosed
US-20080058378-A1 Compounds which have activity at M1 receptor and their uses in medicine. GLAXO GROUP LIMITED (GB) 2008-03-06 US disclosed
WO-2007121416-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2007-10-25 WO disclosed
WO-2007121416-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2007-10-25 WO disclosed
WO-2007121418-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2007-10-25 WO disclosed
WO-2007121418-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2007-10-25 WO disclosed
WO-2007036715-A2 COMPOUNDS WHICH HAVE ACTIVITY AT M1 RECEPTOR AND THEIR USES IN MEDICINE GLAXO GROUP LIMITED (GB) 2007-04-05 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 (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-20080255195-A1 Compounds Which Have Activity at M1 Receptor and Their Uses in Medicine CHRM1, CHRM2, CHRM5 TDP1 2576/4885TSHR 56/4885SMN1; SMN2 4262/4885
US-20240116921-A1 LACTAM (HETERO)ARYLFUSEDPYRIMIDINE DERIVATIVES AS INHIBITORS OF ERBB2 ERBB2, FGFR2, ERBB3 TDP1 2967/4885TSHR 3085/4885SMN1; SMN2 1517/4885
US-20080058378-A1 Compounds which have activity at M1 receptor and their uses in medicine. CHRM1, CHRM2, CHRM5 TDP1 2127/4885TSHR 67/4885SMN1; SMN2 4042/4885

“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.