SCHEMBL9394688

SCHEMBL9394688

Cn1c2ccccc2c2cc3ccccc3nc21

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 4/20 0.59
▸ RXFP1 Q9HBX9 1/20 0.59
▸ KMT2A Q03164 4/20 0.50
▸ MEN1 O00255 3/20 0.50
▸ NR1I2 O75469 1/20 0.50
▸ AHR P35869 1/20 0.50
▸ GPR3 P46089 1/20 0.50
▸ MAPT P10636 5/20 0.49
▸ CASP1 P29466 4/20 0.49
▸ CASP7 P55210 4/20 0.49
▸ LMNA P02545 3/20 0.49
▸ HCRTR1 O43613 2/20 0.49
▸ L3MBTL1 Q9Y468 2/20 0.49
▸ TERT O14746 1/20 0.49
▸ PDE2A O00408 1/20 0.47
▸ PDE3B Q13370 1/20 0.47
▸ PDE3A Q14432 1/20 0.47
▸ SMN1; SMN2 Q16637 2/20 0.45
▸ HSD17B10 Q99714 2/20 0.44
▸ GAA P10253 1/20 0.44

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
SCHEMBL30888893 0.84 MEN1 (0.56) KDM4ERXFP1KMT2AMEN1NR1I2
SCHEMBL29282173 0.84 MEN1 (0.68) KDM4ERXFP1KMT2AMEN1NR1I2
SCHEMBL29202682 0.84 MEN1 (0.56) KDM4ERXFP1KMT2AMEN1NR1I2
SCHEMBL29202622 0.83 ACHE (0.46) KDM4ERXFP1KMT2AMEN1NR1I2
SCHEMBL29202644 0.83 KDM4E (0.52) KDM4ERXFP1KMT2AMEN1NR1I2
SCHEMBL29202651 0.81 KMT2A (0.57) KDM4ERXFP1KMT2AMEN1NR1I2
SCHEMBL29202709 0.81 ALDH1A1 (0.57) KDM4EKMT2AMEN1MAPTLMNA
SCHEMBL18655577 0.80 MAPT (0.67) KDM4ERXFP1KMT2AMEN1MAPT
SCHEMBL29282174 0.79 KDM4E (0.49) KDM4ERXFP1KMT2AMEN1NR1I2
SCHEMBL19271263 0.79 MAPT (0.65) KDM4ERXFP1KMT2AMEN1MAPT

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 4 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
WO-2015147666-A1 N-GUANYL DERIVATIVES OF 9-AMINO-5.1 1 -DIMETHYL-5H-INDOLO[2,3-B]QUINOLINE HAVING CYTOTOXIC ACTIVITY INSTYTUT FARMACEUTYCZNY (PL) 2015-10-01 — — WO disclosed
WO-1994018203-A1 ALKALOID COMPOUNDS EXTRACTED FROM CRYPTOLEPIS SANQUINOLENTA AND USES THEREOF HEALTHSEARCH, INC. (US) 1994-08-18 — — WO disclosed
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