SCHEMBL994700

SCHEMBL994700

O=[N+]([O-])c1cnc2cc(F)c(Br)cc2c1Cl

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 4/20 0.36
ATM Q13315 1/20 0.36
PIN1 Q13526 1/20 0.35
ALDH1A1 P00352 4/20 0.34
HIF1A Q16665 2/20 0.34
CYP3A4 P08684 2/20 0.34
HPGD P15428 1/20 0.34
ALOX15 P16050 1/20 0.34
TSHR P16473 1/20 0.34
TXNRD1 Q16881 1/20 0.34
TXNRD3 Q86VQ6 1/20 0.34
TXNRD2 Q9NNW7 1/20 0.34
MAPT P10636 4/20 0.34
PKM P14618 2/20 0.34
TDO2 P48775 2/20 0.34
VCAM1 P19320 3/20 0.33
MAPK1 P28482 1/20 0.33
EGFR P00533 1/20 0.33
L3MBTL1 Q9Y468 2/20 0.33
PTGES O14684 1/20 0.33

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
SCHEMBL27650679 1.00 TDP1 (0.36) TDP1ATMPIN1ALDH1A1HIF1A
SCHEMBL16486293 0.92 KDM4E (0.36) TDP1ATMPIN1ALDH1A1HIF1A
SCHEMBL4712057 0.85 EGFR (0.39) TDP1ALDH1A1TSHRMAPTPKM
SCHEMBL16470135 0.83 MAPT (0.41) TDP1ATMALDH1A1HIF1AHPGD
SCHEMBL29969235 0.83 CYP1A2 (0.37) TDP1PIN1ALDH1A1TSHRMAPT
SCHEMBL26131871 0.83 CYP1A2 (0.37) TDP1PIN1ALDH1A1TSHRMAPT
SCHEMBL21050767 0.82 MAPT (0.37) TDP1ALDH1A1HIF1ACYP3A4HPGD
SCHEMBL24771867 0.81 PIN1 (0.36) TDP1PIN1ALDH1A1HIF1ACYP3A4
SCHEMBL18114309 0.80 PDGFRB (0.43) PIN1ALDH1A1MAPTEGFRHTT
SCHEMBL25233608 0.77 PDGFRB (0.43) PIN1ALDH1A1MAPTEGFRHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250268873-A1 COMBINATION OF DUAL ATM AND DNA-PK INHIBITORS AND IMMUNOTHERAPEUTIC AGENTS FOR USE IN CANCER THERAPY XRAD THERAPEUTICS, INC. (US) 2025-08-28 US disclosed
CN-119684291-A Dual ATM and DNA-PK inhibitors for use in anti-tumor therapy 艾科思莱德制药公司 2025-03-25 CN disclosed
CN-119661531-A Imidazolone compound as well as preparation method and application thereof 北京富龙康泰生物技术有限公司 2025-03-21 CN disclosed
US-12187742-B2 Dual ATM and DNA-PK inhibitors for use in anti-tumor therapy XRAD THERAPEUTICS, INC. (US) 2025-01-07 US disclosed
EP-4003345-B1 DUAL ATM AND DNA-PK INHIBITORS FOR USE IN ANTI-TUMOR THERAPY XRAD THERAPEUTICS INC (US) 2024-12-04 EP disclosed
CN-114258301-B Dual ATM and DNA-PK inhibitors for use in anti-tumor therapy 艾科思莱德制药公司 2024-11-08 CN disclosed
CN-112469720-B Dual ATM and DNA-PK inhibitors for use in anti-tumor therapy 艾科思莱德制药公司 2024-03-29 CN disclosed
EP-4327877-A2 DUAL ATM AND DNA-PK INHIBITORS FOR USE IN ANTI-TUMOR THERAPY XRad Therapeutics, Inc. (US) 2024-02-28 EP disclosed
EP-4288423-A1 COMBINATION OF DUAL ATM AND DNA-PK INHIBITORS AND IMMUNOTHERAPEUTIC AGENTS FOR USE IN CANCER THERAPY XRad Therapeutics, Inc. (US) 2023-12-13 EP disclosed
CN-117015534-A Combination of dual ATM and DNA-PK inhibitors for cancer therapy and immunotherapeutic agents 艾科思莱德制药公司 2023-11-07 CN disclosed
EP-1687305-B1 1H-IMIDAZOQUINOLINE DERIVATIVES AS PROTEIN KINASE INHIBITORS NOVARTIS AG (CH) 2008-07-09 EP disclosed
EP-1888578-A2 IMIDAZOQUINOLINES AS LIPID KINASE INHIBITORS Novartis AG (CH) 2008-02-20 EP disclosed
US-20070213355-A1 1H-Imidazo[4,5-C]Quinoline Derivatives in the Treatment of Protein Kinase Dependent Diseases CAPRARO HANS-GEORG 2007-09-13 US disclosed
CN-1902200-A 1h-imidazoquinoline derivatives as protein kinase inhibitors NOVARTIS AG (CH) 2007-01-24 CN disclosed
CN-1882586-A 1H-imidazo[4,5-C]quinoline derivatives in the treatment of protein kinase dependent diseases NOVARTIS AG (CH) 2006-12-20 CN disclosed
WO-2006122806-A2 1,3-DIHYDRO-IMIDAZO [4,5-C] QUINOLIN-2-ONES AS LIPID KINASE INHIBITORS NOVARTIS AG (CH) 2006-11-23 WO disclosed
EP-1689747-A1 1H-IMIDAZO [4,5-C] QUINOLINE DERIVATIVES IN THE TREATMENT OF PROTEIN KINASE DEPENDENT DISEASES Novartis AG (CH) 2006-08-16 EP disclosed
EP-1687305-A1 1H-IMIDAZOQUINOLINE DERIVATIVES AS PROTEIN KINASE INHIBITORS Novartis AG (CH) 2006-08-09 EP disclosed
WO-2005054237-A1 1H-IMIDAZOQUINOLINE DERIVATIVES AS PROTEIN KINASE INHIBITORS NOVARTIS AG (CH) 2005-06-16 WO disclosed
WO-2005054238-A1 1H-IMIDAZO[4,5-C]QUINOLINE DERIVATIVES IN THE TREATMENT OF PROTEIN KINASE DEPENDENT DISEASES NOVARTIS AG (CH) 2005-06-16 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-20070213355-A1 1H-Imidazo[4,5-C]Quinoline Derivatives in the Treatment of Protein Kinase Dependent Diseases ABL1, PRKCA, PRKCQ TDP1 1148/4885ATM 708/4885PIN1 3192/4885
US-12187742-B2 Dual ATM and DNA-PK inhibitors for use in anti-tumor therapy ATM, CHEK2, CHEK1 TDP1 15/4885ATM 1/4885PIN1 2919/4885
US-20250268873-A1 COMBINATION OF DUAL ATM AND DNA-PK INHIBITORS AND IMMUNOTHERAPEUTIC AGENTS FOR USE IN CANCER THERAPY ATM, CHEK2, CHEK1 TDP1 34/4885ATM 1/4885PIN1 2576/4885

“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.