SCHEMBL29202634

SCHEMBL29202634

Cn1c2ccc(C(=O)O)cc2c2cc3ccccc3nc21

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 5/20 0.61
▸ RXFP1 Q9HBX9 2/20 0.49
▸ HPGD P15428 2/20 0.48
▸ ALDH1A1 P00352 1/20 0.48
▸ MEN1 O00255 4/20 0.47
▸ KMT2A Q03164 4/20 0.47
▸ MAPT P10636 3/20 0.47
▸ GAA P10253 1/20 0.47
▸ HTT P42858 1/20 0.47
▸ SMN1; SMN2 Q16637 1/20 0.47
▸ HSD17B10 Q99714 1/20 0.45
▸ PTGER4 P35408 3/20 0.45
▸ NR1I2 O75469 1/20 0.45
▸ AHR P35869 1/20 0.45
▸ HCRTR1 O43613 2/20 0.44
▸ CASP1 P29466 1/20 0.44
▸ CASP7 P55210 1/20 0.44
▸ FGFR1 P11362 1/20 0.44
▸ HCAR3 P49019 1/20 0.43
▸ MGAM O43451 1/20 0.43

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
SCHEMBL29282173 0.80 MEN1 (0.68) KDM4ERXFP1MEN1KMT2AMAPT
SCHEMBL9394688 0.79 KDM4E (0.59) KDM4ERXFP1HPGDALDH1A1MEN1
SCHEMBL29202644 0.79 KDM4E (0.52) KDM4ERXFP1HPGDALDH1A1MEN1
SCHEMBL69291 0.77 KDM4E (0.83) KDM4EHPGDALDH1A1MAPTHSD17B10
SCHEMBL29202651 0.77 KMT2A (0.57) KDM4ERXFP1HPGDALDH1A1MEN1
SCHEMBL30850787 0.76 KDM4E (1.00) KDM4EHPGDALDH1A1MEN1KMT2A
SCHEMBL3102894 0.76 KDM4E (1.00) KDM4EHPGDALDH1A1MEN1KMT2A
SCHEMBL24016050 0.73 TEAD1 (0.61) KDM4EHPGDALDH1A1MEN1KMT2A
SCHEMBL31498242 0.70 MGAM (0.61) KDM4ERXFP1HPGDALDH1A1MEN1
SCHEMBL9051022 0.70 MGAM (0.56) KDM4ERXFP1HPGDALDH1A1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117987851-A Method for preparing indolo [2,3-b ] quinoline compounds by electrochemical iodine catalysis 山东第二医科大学 2024-05-07 — — CN disclosed
CN-117946104-A Preparation method of iodine-mediated indolo [2,3-b ] quinoline compound in water phase 山东第二医科大学 2024-04-30 — — CN disclosed
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