SCHEMBL199306

SCHEMBL199306

c1cc(-n2cccn2)nc(-n2cccn2)c1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.65
KDM4E B2RXH2 4/20 0.65
NPC1 O15118 3/20 0.52
MAPK1 P28482 3/20 0.52
SMN1; SMN2 Q16637 3/20 0.47
MAPT P10636 2/20 0.47
RAB9A P51151 2/20 0.47
NOTUM Q6P988 1/20 0.47
ATM Q13315 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
LMNA P02545 3/20 0.44
KMT2A Q03164 3/20 0.43
MEN1 O00255 2/20 0.43
GAA P10253 1/20 0.43
G6PD P11413 1/20 0.43
GRM5 P41594 2/20 0.42
ADORA2A P29274 2/20 0.41
ADORA1 P30542 2/20 0.41
GLA P06280 1/20 0.41
NLRP3 Q96P20 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
SCHEMBL28812535 0.98 ALDH1A1 (0.63) ALDH1A1KDM4ENPC1MAPK1SMN1; SMN2
SCHEMBL31519065 0.98 ALDH1A1 (0.63) ALDH1A1KDM4ENPC1MAPK1SMN1; SMN2
SCHEMBL31517328 0.86 ALDH1A1 (0.50) ALDH1A1KDM4ENPC1MAPK1MAPT
SCHEMBL4289 0.86 KDM4E (0.50) ALDH1A1KDM4ENPC1MAPK1SMN1; SMN2
SCHEMBL13822150 0.86 KDM4E (0.50) ALDH1A1KDM4ENPC1MAPK1NOTUM
SCHEMBL31653378 0.86 KDM4E (0.50) ALDH1A1KDM4ENPC1MAPK1SMN1; SMN2
SCHEMBL13473987 0.86 KDM4E (0.50) ALDH1A1KDM4ENPC1MAPK1SMN1; SMN2
SCHEMBL3570306 0.86 KDM4E (0.50) ALDH1A1KDM4ENPC1MAPK1SMN1; SMN2
SCHEMBL30261053 0.86 KDM4E (0.50) ALDH1A1KDM4ENPC1MAPK1SMN1; SMN2
SCHEMBL28030385 0.86 KDM4E (0.50) ALDH1A1KDM4ENPC1MAPK1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122059983-A Reductive silanization method of nickel-catalyzed alpha-benzoylalkyl bromide and chlorosilane on activated olefin 大连理工大学 2026-05-19 CN claimed
CN-118186417-A Electrochemical construction of C (sp)3)-C(sp3) Method for bonding and compound prepared by same 南开大学 2024-06-14 CN claimed
CN-117623925-A Method for deoxidizing and converting photocatalytic alcohol 同济大学 2024-03-01 CN claimed
CN-116926582-A Method for synthesizing ketone by electrochemical cross-reduction coupling 四川大学 2023-10-24 CN claimed
US-20220359824-A1 PEROVSKITE SEMICONDUCTOR DEVICES CAMBRIDGE ENTERPRISE LIMITED (GB) 2022-11-10 US claimed
CN-110372756-A Bivalent platinum complex and preparation method and application thereof 南京工业大学 2019-10-25 CN claimed
CN-122059983-A Reductive silanization method of nickel-catalyzed alpha-benzoylalkyl bromide and chlorosilane on activated olefin 大连理工大学 2026-05-19 CN disclosed
US-20250281084-A1 COMPOSITION, COATING, AND METHOD FOR REDUCING EARLY/LATE SENSOR ATTENUATION OF ANALYTE BIOSENSOR ABBOTT DIABETES CARE INC. 2025-09-11 US disclosed
US-20250213152-A1 BACKGROUND INTERFERENCE MITIGATION FOR HIGH SENSITIVITY KETONE SENSING ABBOTT DIABETES CARE INC. (US) 2025-07-03 US disclosed
WO-2025137203-A1 GLUCOSE OXIDASE SENSORS WITH IMPROVED STABILITY ABBOTT DIABETES CARE, INC. (US) 2025-06-26 WO disclosed
US-20250194964-A1 GLUCOSE OXIDASE SENSORS WITH IMPROVED STABILITY ABBOTT DIABETES CARE, INC. 2025-06-19 US disclosed
CN-119948022-A Process for producing macrolide compounds 卫材R&D管理有限公司 2025-05-06 CN disclosed
WO-2025082616-A1 ENERGY ADAPTER MODULE FOR A CELL HELMHOLTZ-ZENTRUM FÜR UMWELTFORSCHUNG GMBH - UFZ (DE) 2025-04-24 WO disclosed
US-5929232-A REACTING NUCLEOPHILE AND RACEMIC MIXTURE OF CHIRAL CYCLIC SUBSTRATE IN PRESENCE OF NON-RACEMIC CHIRAL CATALYST TO PRODUCE STEREOISOMERICALLY ENRICHED CYCLIC SUBSTRATE BY KINETIC RESOLUTION PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1999-07-27 US disclosed
WO-1999036375-A1 ASYMMETRIC CYCLOADDITION REACTIONS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1999-07-22 WO disclosed
EP-0626068-B1 LUMINESCENT LANTHANIDE CHELATES WALLAC OY (FI) 1999-05-06 EP disclosed
EP-0817765-A1 STEREOSELECTIVE RING OPENING REACTIONS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1998-01-14 EP disclosed
US-5665890-A CHEMICAL SYNTHESIS COMPRISING REACTING A NUCLEOPHILE AND A CHIRAL OR PROCHIRAL CYCLIC SUBSTRATE PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1997-09-09 US disclosed
US-5571897-A Luminescent lanthanide chelates WALLAC OY (FI) 1996-11-05 US disclosed
WO-1996028402-A1 STEREOSELECTIVE RING OPENING REACTIONS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1996-09-19 WO disclosed