SCHEMBL1845696

SCHEMBL1845696

FC(F)c1ccc2ccccc2n1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NCF1 P14598 3/20 0.46
CYP1A2 P05177 2/20 0.46
NOS2 P35228 1/20 0.46
BACE1 P56817 1/20 0.46
CA12 O43570 1/20 0.46
CA9 Q16790 1/20 0.46
ALDH1A1 P00352 5/20 0.45
HSD17B10 Q99714 1/20 0.45
POLB P06746 1/20 0.44
MAPT P10636 2/20 0.42
GLA P06280 1/20 0.42
HPGD P15428 1/20 0.42
ACHE P22303 1/20 0.42
MGAM O43451 1/20 0.41
S1PR3 Q99500 1/20 0.41
KDM4E B2RXH2 2/20 0.40
PRNP P04156 1/20 0.40
MAPK10 P53779 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
RXFP1 Q9HBX9 1/20 0.40

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
SCHEMBL30106721 1.00 NCF1 (0.46) NCF1CYP1A2NOS2BACE1CA12
Selenium SCHEMBL32667944 0.96 NCF1 (0.43) NCF1CYP1A2NOS2BACE1CA12
SCHEMBL21580901 0.83 NCF1 (0.43) NCF1CYP1A2NOS2BACE1CA12
SCHEMBL10020390 0.82 ALDH1A1 (0.53) NCF1CYP1A2NOS2BACE1CA12
SCHEMBL9009627 0.81 NCF1 (0.50) NCF1CYP1A2NOS2BACE1CA12
SCHEMBL2028207 0.79 S1PR3 (0.47) NCF1CYP1A2NOS2BACE1CA12
SCHEMBL1129147 0.77 NCF1 (0.46) NCF1CYP1A2NOS2BACE1CA12
SCHEMBL3294485 0.77 NCF1 (0.46) NCF1CYP1A2NOS2BACE1CA12
SCHEMBL827081 0.77 CYP1A2 (0.52) NCF1CYP1A2NOS2BACE1CA12
Bromide SCHEMBL29161153 0.76 CYP1A2 (0.50) NCF1CYP1A2NOS2BACE1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260027104-A1 NOVEL NAPHTHYL AND ISOQUINOLINE SULFONAMIDE DERIVATIVES HOFFMANN-LA ROCHE INC. (US) 2026-01-29 US disclosed
WO-2024006881-A1 WEE1 DEGRADING COMPOUNDS AND USES THEREOF BRISTOL-MYERS SQUIBB COMPANY (US) 2024-01-04 WO disclosed
CN-116472292-A Modified proteins and protein degrading agents 上海睿跃生物科技有限公司 2023-07-21 CN disclosed
CN-116217478-A Synthesis method of 6-amino-3-difluoromethyl quinoline 苏州康润医药有限公司 2023-06-06 CN disclosed
EP-4157888-A1 MODIFIED PROTEINS AND PROTEIN DEGRADERS Cullgen (Shanghai), Inc. (CN) 2023-04-05 EP disclosed
EP-4101843-A1 METHOD FOR PRODUCING AROMATIC HETEROCYCLIC RING-SUBSTITUTED DIFLUOROACETIC ACID DERIVATIVE AGC INC. (JP) 2022-12-14 EP disclosed
EP-4101842-A1 METHOD FOR PRODUCING DIFLUOROMETHYL-SUBSTITUTED AROMATIC HETEROCYCLIC COMPOUND AGC INC. (JP) 2022-12-14 EP disclosed
WO-2022042707-A1 CYCLIC-AMP RESPONSE ELEMENT BINDING PROTEIN (CBP) AND/OR ADENOVIRAL E1A BINDING PROTEIN OF 300 KDA (P300) DEGRADATION COMPOUNDS AND METHODS OF USE CULLGEN (SHANGHAI) , INC. (CN) 2022-03-03 WO disclosed
WO-2021239117-A1 MODIFIED PROTEINS AND PROTEIN DEGRADERS CULLGEN (SHANGHAI) , INC. (CN) 2021-12-02 WO disclosed
CN-112939729-A Method for carrying out hydrogen-deuterium exchange reaction on difluoromethyl aromatic hydrocarbon under base catalysis 中国人民大学 2021-06-11 CN disclosed
US-20090018012-A1 Process for Producing Olefin Copolymerization Catalyst and Process for Producing Olefin Copolymer SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-01-15 US disclosed
CN-101195672-A Method for producing olefin-copolymerization catalyst and method for producing olefin-copolymers SUMITOMO CHEMICAL CO (JP) 2008-06-11 CN disclosed
CN-1320122-A Pyrazole derivatives and salts thereof DAIICHI SEIYAKU CO (JP) 2001-10-31 CN disclosed
CN-1043761-C Fluorinated hydroxyalkylquinoline acids as leukotriene antagonists MERCK FROSST CANADA INC (CA) 1999-06-23 CN disclosed
EP-0565185-B1 Quinoline derivatives as leukotriene antagonists MERCK FROSST CANADA INC (CA) 1998-07-08 EP disclosed
CN-1152915-A Quinoline derivatives as leukotriene antagonists LEO PHARM PROD LTD (DK) 1997-06-25 CN disclosed
CN-1083052-A Fluorine-containing hydroxyalkylquinolinacids acids as leukotriene antagonists MERCK FROSST CANADA INC (CA) 1994-03-02 CN disclosed
US-5270324-A Fluorinated hydroxyalkylquinoline acids as leukotriene antagonists MERCK FROSST CANADA, INC. (CA) 1993-12-14 US disclosed
WO-1993021159-A1 QUINOLINE DERIVATIVES AS LEUKOTRIENE ANTAGONISTS MERCK FROSST CANADA INC. (CA) 1993-10-28 WO disclosed
EP-0565185-A1 Quinoline derivatives as leukotriene antagonists MERCK FROSST CANADA INC. (CA) 1993-10-13 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-20260027104-A1 NOVEL NAPHTHYL AND ISOQUINOLINE SULFONAMIDE DERIVATIVES CBR3, HAX1, CBR1 NCF1 1316/4885CYP1A2 520/4885NOS2 1682/4885

“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.