SCHEMBL29548142

SCHEMBL29548142

[N-]=[N+]=C1C(=O)Nc2ccccc21

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LRRK2 Q5S007 4/20 0.55
ACVR1 Q04771 2/20 0.55
MAOA P21397 1/20 0.55
MAOB P27338 1/20 0.55
PDGFRA P16234 1/20 0.55
FER P16591 1/20 0.55
LTK P29376 1/20 0.55
CDK8 P49336 1/20 0.55
DYRK1B Q9Y463 1/20 0.55
ALDH1A1 P00352 4/20 0.44
MAPT P10636 4/20 0.44
IDO1 P14902 3/20 0.44
SMN1; SMN2 Q16637 3/20 0.44
NPSR1 Q6W5P4 3/20 0.44
KDM4E B2RXH2 1/20 0.44
PKM P14618 1/20 0.44
MAPK1 P28482 1/20 0.44
GSK3B P49841 2/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
LMNA P02545 2/20 0.42

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
SCHEMBL10627555 1.00 LRRK2 (0.55) LRRK2ACVR1MAOAMAOBPDGFRA
SCHEMBL10713179 0.90 LRRK2 (0.46) LRRK2ACVR1MAOAMAOBPDGFRA
SCHEMBL6670395 0.89 MAOA (0.62) LRRK2ACVR1MAOAMAOBPDGFRA
SCHEMBL29409246 0.82 GSK3B (0.62) LRRK2ACVR1MAOAMAOBPDGFRA
SCHEMBL29011572 0.76 LRRK2 (0.36) LRRK2ACVR1MAOAMAOBPDGFRA
SCHEMBL2420711 0.75 LRRK2 (0.90) LRRK2ACVR1MAOAMAOBPDGFRA
SCHEMBL366728 0.75
SCHEMBL11546561 0.74 TGM2 (0.61) LRRK2MAOAMAOBIDO1TGM2
SCHEMBL6428222 0.74 CSNK1G1 (0.45) LRRK2ACVR1MAOAMAOBALDH1A1
SCHEMBL1964262 0.74 LRRK2 (0.46) LRRK2MAOAMAOBMEN1KMT2A

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118146227-A Synthesis method of spiro indolone derivative 中国科学院大连化学物理研究所 2024-06-07 CN claimed
CN-110551057-B Chiral 3,3-disubstituted oxindole derivative and synthesis method and application thereof 华东师范大学 2023-02-07 CN claimed
CN-115028645-A Synthesis method of bisindolone [ spiro ] benzodihydrofuran compound 河南师范大学 2022-09-09 CN claimed
CN-113185523-B Synthetic method of 3-indolone [ spiro ] -3H-indole compound 河南师范大学 2022-04-08 CN claimed
CN-121135732-A Indolone spiro pyrroline compound, synthesis method thereof and anticancer activity 河南师范大学 2025-12-16 CN disclosed
CN-118146227-A Synthesis method of spiro indolone derivative 中国科学院大连化学物理研究所 2024-06-07 CN disclosed
CN-117567353-A Indolone spironorcarane diene compound with anticancer activity and preparation method and application thereof 常州大学 2024-02-20 CN disclosed
CN-110551057-B Chiral 3,3-disubstituted oxindole derivative and synthesis method and application thereof 华东师范大学 2023-02-07 CN disclosed
CN-110551057-B Chiral 3,3-disubstituted oxindole derivative and synthesis method and application thereof 华东师范大学 2023-02-07 CN disclosed
CN-115028645-A Synthesis method of bisindolone [ spiro ] benzodihydrofuran compound 河南师范大学 2022-09-09 CN disclosed
CN-115028645-A Synthesis method of bisindolone [ spiro ] benzodihydrofuran compound 河南师范大学 2022-09-09 CN disclosed
CN-113185523-B Synthetic method of 3-indolone [ spiro ] -3H-indole compound 河南师范大学 2022-04-08 CN disclosed
CN-113185523-B Synthetic method of 3-indolone [ spiro ] -3H-indole compound 河南师范大学 2022-04-08 CN disclosed