SCHEMBL377777

SCHEMBL377777

O=[N+]([O-])c1ccc(F)cc1C(F)(F)F

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ATM Q13315 1/20 0.60
TDP1 Q9NUW8 1/20 0.60
SIRT6 Q8N6T7 1/20 0.51
AR P10275 11/20 0.50
CYP3A4 P08684 3/20 0.50
LMNA P02545 2/20 0.50
CYP1A2 P05177 2/20 0.50
CYP2C9 P11712 2/20 0.50
TSHR P16473 2/20 0.50
CYP2C19 P33261 2/20 0.50
SMN1; SMN2 Q16637 2/20 0.50
PGR P06401 2/20 0.50
CES2 O00748 1/20 0.50
ABCB11 O95342 1/20 0.50
ALDH1A1 P00352 1/20 0.50
GLA P06280 1/20 0.50
ADORA3 P0DMS8 1/20 0.50
CHRM1 P11229 1/20 0.50
ALOX15 P16050 1/20 0.50
TBXA2R P21731 1/20 0.50

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
SCHEMBL29788520 1.00 ATM (0.60) ATMTDP1SIRT6ARCYP3A4
SCHEMBL9504655 0.85 TDP1 (0.49) ATMTDP1SIRT6ARCYP3A4
SCHEMBL15074725 0.85 ATM (0.56) ATMTDP1SIRT6ARCYP3A4
SCHEMBL11521456 0.85 ATM (0.49) ATMTDP1SIRT6ARCYP3A4
SCHEMBL4506814 0.85 TDP1 (0.55) ATMTDP1SIRT6ARCYP3A4
SCHEMBL7807883 0.83 TDP1 (0.58) ATMTDP1SIRT6ARCYP3A4
SCHEMBL9491928 0.82 ATM (0.49) ATMTDP1SIRT6ARCYP3A4
SCHEMBL31138869 0.81 ALDH1A1 (0.53) TDP1SIRT6ARCYP3A4LMNA
SCHEMBL2639009 0.81 SIRT6 (0.51) TDP1SIRT6ARCYP3A4LMNA
SCHEMBL1998640 0.81 CYP3A4 (0.52) TDP1SIRT6ARCYP3A4LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118084671-A High-safety 5-fluoro-2-nitro benzotrifluoride and synthetic method thereof 江苏优普生物化学科技股份有限公司 2024-05-28 CN claimed
CN-102898301-A Preparation method of 2-bromine-3-fluorobenzoic acid CHEN WEIDONG 2013-01-30 CN claimed
CN-101602677-A Three (3-trifluoromethyl-4-amino-benzene) amine and preparation method thereof UNIV JILIN (CN) 2009-12-16 CN claimed
US-4470930-A Preparation of nuclear chlorinated aromatic compounds OCCIDENTAL CHEMICAL CORPORATION (US) 1984-09-11 US claimed
US-20260098032-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION PMV PHARMACEUTICALS INC (US) 2026-04-09 US disclosed
US-12583815-B2 Inhibitors of YAP/TAZ-TEAD oncoproteins, synthesis and use thereof BRIDGENE BIOSCIENCES, INC. (US) 2026-03-24 US disclosed
EP-4644387-A2 METHODS AND COMPOUNDS FOR RESTORING MUTANT P53 FUNCTION PMV Pharmaceuticals, Inc. (US) 2025-11-05 EP disclosed
EP-4644388-A1 FIVE-MEMBERED HETEROARYL COMPOUND AND AGRICULTURAL AND HORTICULTURAL BACTERICIDE Nippon Soda Co., Ltd. (JP) 2025-11-05 EP disclosed
US-12428406-B2 Methods and compounds for restoring mutant p53 function PMV PHARMACEUTICALS, INC. (US) 2025-09-30 US disclosed
CN-120136750-A Diamino thioether compound and application thereof in self-repairing polyimide optical film 华中科技大学 2025-06-13 CN disclosed
CN-120081802-A Heterocyclic substituted benzamide derivative and application thereof 南华大学附属第一医院 2025-06-03 CN disclosed
CN-119080580-B Preparation method of 2-bromo-5-fluorobenzotrifluoride 内蒙古大中实业化工有限公司 2025-02-18 CN disclosed
EP-0166533-A1 Quinolone inotropic agents Pfizer Limited (GB) 1986-01-02 EP disclosed
EP-0159388-A2 Preparation of nuclear chlorinated compounds OCCIDENTAL CHEMICAL CORPORATION (US) 1985-10-30 EP disclosed
US-4470930-A Preparation of nuclear chlorinated aromatic compounds OCCIDENTAL CHEMICAL CORPORATION (US) 1984-09-11 US disclosed
US-4469893-A Method for the preparation of nitrodiphenyl ethers OCCIDENTAL CHEMICAL CORPORATION (US) 1984-09-04 US disclosed
US-4424396-A ARYL HALIDE, A-AMINOACID OCCIDENTAL CHEMICAL CORPORATION (US) 1984-01-03 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

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-12583815-B2 Inhibitors of YAP/TAZ-TEAD oncoproteins, synthesis and use thereof YAP1, TEAD1, TEAD2 ATM 521/4885TDP1 2252/4885SIRT6 2858/4885
US-12428406-B2 Methods and compounds for restoring mutant p53 function TP53, TP53BP1, KRAS ATM 115/4885TDP1 92/4885SIRT6 1733/4885
US-20260098032-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION TP53, TP53BP1, MDM2 ATM 129/4885TDP1 71/4885SIRT6 1904/4885

“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.