SCHEMBL30608271

SCHEMBL30608271

Cc1c(C(=O)c2ccccc2)oc2cccc(Cl)c12

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 6/20 0.59
RAB9A P51151 5/20 0.59
L3MBTL1 Q9Y468 1/20 0.59
ALDH1A1 P00352 3/20 0.48
KMT2A Q03164 2/20 0.48
MEN1 O00255 1/20 0.48
MAPT P10636 5/20 0.48
TSHR P16473 1/20 0.46
LMNA P02545 1/20 0.46
GAA P10253 1/20 0.46
EDNRA P25101 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.43
NMT2 O60551 1/20 0.43
NMT1 P30419 1/20 0.43
POLB P06746 1/20 0.43
KDM1A O60341 1/20 0.43
TTR P02766 3/20 0.42
PTPN1 P18031 1/20 0.42
RXFP1 Q9HBX9 1/20 0.41
THRB P10828 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
SCHEMBL27590200 0.84 EDNRA (0.62) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL15012161 0.83 NPC1 (0.61) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL30780353 0.82 NPC1 (0.63) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL10439862 0.80 TTR (0.46) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL11501126 0.78 NPC1 (0.55) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL30608270 0.78 NPC1 (0.66) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL11097183 0.77 KDM1A (0.43) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
Hydrochloric Acid SCHEMBL11500841 0.77 NPC1 (0.53) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL31384138 0.74 MCL1 (0.71) NPC1RAB9AL3MBTL1ALDH1A1KMT2A
SCHEMBL3699309 0.73 SMN1; SMN2 (0.69) NPC1RAB9AL3MBTL1ALDH1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116874452-A Synthesis method for synthesizing 2-methylbenzofuran structural compound by taking calcium carbide as alkynyl source 宁夏大学 2023-10-13 CN disclosed