SCHEMBL28583923

SCHEMBL28583923

COc1ccc(C(=O)/C(=C(\N)c2ccccc2)n2nnc3ccccc32)cc1OC

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ F12 P00748 4/20 0.69
▸ KMT2A Q03164 5/20 0.56
▸ ALDH1A1 P00352 4/20 0.56
▸ MEN1 O00255 2/20 0.56
▸ SMN1; SMN2 Q16637 1/20 0.56
▸ MGAM O43451 7/20 0.51
▸ AMY1A P0DUB6 7/20 0.51
▸ GAA P10253 7/20 0.51
▸ SI P14410 7/20 0.51
▸ MGAM2 Q2M2H8 7/20 0.51
▸ MIF P14174 1/20 0.51
▸ HPGD P15428 3/20 0.49
▸ F2 P00734 1/20 0.49
▸ SLC9A1 P19634 1/20 0.49
▸ NPC1 O15118 2/20 0.48
▸ RAB9A P51151 2/20 0.48
▸ HDAC3 O15379 1/20 0.47
▸ HDAC4 P56524 1/20 0.47
▸ HDAC1 Q13547 1/20 0.47
▸ HDAC7 Q8WUI4 1/20 0.47

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
SCHEMBL29502827 1.00 F12 (0.69) F12KMT2AALDH1A1MEN1SMN1; SMN2
SCHEMBL28583982 0.90 F12 (0.71) F12KMT2AALDH1A1MEN1SMN1; SMN2
SCHEMBL29502831 0.84 GAA (0.63) F12KMT2AALDH1A1MGAMAMY1A
SCHEMBL28579185 0.84 GAA (0.63) F12KMT2AALDH1A1MGAMAMY1A
SCHEMBL27397036 0.82 F12 (1.00) F12KMT2AALDH1A1MEN1SMN1; SMN2
SCHEMBL29502829 0.81 GAA (0.56) F12KMT2AALDH1A1MEN1SMN1; SMN2
SCHEMBL28594361 0.79 GAA (0.63) F12KMT2AALDH1A1MGAMAMY1A
SCHEMBL28915566 0.76 GAA (0.52) F12KMT2AALDH1A1SMN1; SMN2MGAM
SCHEMBL28580426 0.75 MGAM (0.60) F12KMT2AALDH1A1MEN1SMN1; SMN2
SCHEMBL28589160 0.75 F12 (0.60) F12KMT2AALDH1A1MEN1SMN1; SMN2

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-113045508-B Method for synthesizing diaminoalkene by NBS (N-bromosuccinimide) to promote polarity reversal of enaminone 河南科技大学 2022-04-22 — — CN disclosed
CN-113045508-A Method for synthesizing diaminoalkene by NBS (N-bromosuccinimide) to promote polarity reversal of enaminone 河南科技大学 2021-06-29 — — CN disclosed
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