SCHEMBL2425907

SCHEMBL2425907

Oc1cc(C(F)(F)F)nc2ccccc12

nearest known ligand 0.58

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ADORA2A P29274 1/20 0.58
ADORA1 P30542 1/20 0.58
TLR7 Q9NYK1 1/20 0.50
ADRB2 P07550 1/20 0.50
MAPK1 P28482 1/20 0.48
LMNA P02545 1/20 0.47
POLB P06746 1/20 0.47
IGF1R P08069 6/20 0.47
BACE1 P56817 1/20 0.46
KMT2A Q03164 1/20 0.46
MYC P01106 1/20 0.44
MAX P61244 1/20 0.44
NT5E P21589 1/20 0.44
MAPT P10636 3/20 0.43
GAA P10253 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
ELANE P08246 1/20 0.41

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
Methane SCHEMBL11402189 0.98 ADORA2A (0.56) ADORA2AADORA1TLR7ADRB2MAPK1
Methane SCHEMBL5243858 0.96 ADORA2A (0.55) ADORA2AADORA1TLR7ADRB2MAPK1
Ethane SCHEMBL8441819 0.96 ADORA2A (0.55) ADORA2AADORA1TLR7ADRB2MAPK1
SCHEMBL28019418 0.82 NT5E (0.56) ADORA2AADORA1LMNAPOLBNT5E
SCHEMBL3618520 0.80 ADORA2A (0.56) ADORA2AADORA1TLR7ADRB2MAPK1
SCHEMBL31265529 0.80 ADORA2A (0.56) ADORA2AADORA1TLR7ADRB2MAPK1
SCHEMBL693661 0.79 NT5E (0.62) ADORA2AADORA1TLR7ADRB2MAPK1
SCHEMBL3300391 0.79 BACE1 (0.66) ADORA2AADORA1TLR7ADRB2MAPK1
SCHEMBL28311336 0.79 ADORA2A (0.55) ADORA2AADORA1TLR7ADRB2MAPK1
SCHEMBL10643394 0.79 L3MBTL1 (0.63) ADORA2AADORA1TLR7ADRB2MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120136851-A Preparation method and application of quinoline ester compound 楚雄师范学院 2025-06-13 CN claimed
CN-117397690-A Application of 2, 8-bis (trifluoromethyl) -4-hydroxyquinoline derivative in preventing and controlling agricultural bacteria 兰州大学 2024-01-16 CN claimed
CN-116991036-A Fluorine-silicon modified polyurethane photoresist and preparation method thereof 常州大学 2023-11-03 CN claimed
CN-115197134-A Preparation method and application of camphorsulfonate compounds 南京林业大学 2022-10-18 CN claimed
CN-112608275-A Application of 2, 8-bis (trifluoromethyl) -4-hydroxyquinoline derivative in preparation and prevention and treatment of agricultural diseases 兰州大学 2021-04-06 CN claimed
EP-2205083-A1 SUBSTITUTED ARYL SULFONE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS Merck Sharp & Dohme Corp. (US) 2010-07-14 EP claimed
WO-2009045382-A1 SUBSTITUTED ARYL SULFONE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS MERCK & CO., INC. (US) 2009-04-09 WO claimed
WO-1998033786-A9 ACCELERATED CATALYSIS OF OLEFINIC EPOXIDATIONS 1998-12-30 WO claimed
WO-1998033786-A1 ACCELERATED CATALYSIS OF OLEFINIC EPOXIDATIONS THE SCRIPPS RESEARCH INSTITUTE (US) 1998-08-06 WO claimed
US-12459921-B2 Isoindoline compound, preparation method, pharmaceutical composition and use thereof SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2025-11-04 US disclosed
CN-120136851-A Preparation method and application of quinoline ester compound 楚雄师范学院 2025-06-13 CN disclosed
EP-4055014-B1 PYRROLIDINE AND PIPERIDINE COMPOUNDS YUHAN CORP (KR) 2025-04-30 EP disclosed
CN-119139301-A Application of 2, 8-trifluoromethyl quinoline derivative in preventing and treating cow mastitis pathogenic bacteria 兰州大学 2024-12-17 CN disclosed
CN-115197134-B Preparation method and application of camphorsulfonate compounds 南京林业大学 2024-07-30 CN disclosed
EP-0055061-A1 Male gametocide method in small grain plants UNION CARBIDE CORPORATION (US) 1982-06-30 EP disclosed
EP-0049555-A1 2-Trifluoromethyl-4-hydroxy-3 quinoline-carboxylic-acid derivatives and their preparation ROUSSEL-UCLAF (FR) 1982-04-14 EP disclosed
EP-0049555-A1 2-Trifluoromethyl-4-hydroxy-3 quinoline-carboxylic-acid derivatives and their preparation ROUSSEL-UCLAF (FR) 1982-04-14 EP disclosed
US-4267333-A Preparation of 2-trifluoromethyl cinchoninic acids UNION CARBIDE AGRICULTURAL PRODUCTS COMPANY, INC. (US) 1981-05-12 US disclosed
US-4251661-A Preparation of 2-trifluoromethyl cinchoninic acids UNION CARBIDE CORPORATION (US) 1981-02-17 US disclosed
EP-0012639-A2 Quinolein-3-carboxylic acid derivatives, process for their preparation, their use in medicines and pharmaceutical compositions containing them ROUSSEL-UCLAF (FR) 1980-06-25 EP 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 (1 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-12459921-B2 Isoindoline compound, preparation method, pharmaceutical composition and use thereof CUL4B, CUL4A, UBQLN1 ADORA2A 3261/4885ADORA1 3126/4885TLR7 2332/4885

“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.