SCHEMBL29396406

SCHEMBL29396406

COc1ccccc1P(=O)(CCP(=O)(c1ccccc1)c1ccccc1OC)c1ccccc1

nearest known ligand 0.73

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 4/20 0.73
▸ MEN1 O00255 3/20 0.73
▸ L3MBTL1 Q9Y468 2/20 0.60
▸ HTT P42858 2/20 0.60
▸ ALDH1A1 P00352 4/20 0.47
▸ POLB P06746 1/20 0.46
▸ MAPT P10636 2/20 0.46
▸ GAA P10253 2/20 0.46
▸ ALPG P10696 1/20 0.46
▸ ALOX12 P18054 1/20 0.46
▸ NPY1R P25929 1/20 0.46
▸ NPY2R P49146 1/20 0.46
▸ NPSR1 Q6W5P4 1/20 0.46
▸ HIF1A Q16665 1/20 0.44
▸ LMNA P02545 2/20 0.44
▸ RECQL P46063 1/20 0.44
▸ NPC1 O15118 1/20 0.42
▸ CTSD P07339 1/20 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
SCHEMBL3807805 1.00 KMT2A (0.73) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL28685764 1.00 KMT2A (0.73) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL24308948 0.89 KMT2A (0.79) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL23658897 0.89 KMT2A (0.64) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL23658968 0.89 KMT2A (0.64) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL15715540 0.86 KMT2A (0.69) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL3787871 0.82 KMT2A (0.52) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL31326108 0.82 MEN1 (0.56) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL6828371 0.80 KMT2A (0.61) KMT2AMEN1L3MBTL1HTTALDH1A1
SCHEMBL23658965 0.79 KMT2A (0.60) KMT2AMEN1L3MBTL1HTTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114133412-B Preparation method of chiral 1, 2-bis [ (2-methoxyphenyl) phenylphosphinyl ] ethane 河南工程学院 2023-11-07 — — CN claimed
CN-117447464-A Method for producing optically active compound 首日生物制药公司 2024-01-26 — — CN disclosed
CN-114133412-B Preparation method of chiral 1, 2-bis [ (2-methoxyphenyl) phenylphosphinyl ] ethane 河南工程学院 2023-11-07 — — CN disclosed
CN-114133412-B Preparation method of chiral 1, 2-bis [ (2-methoxyphenyl) phenylphosphinyl ] ethane 河南工程学院 2023-11-07 — — CN disclosed
CN-114133412-B Preparation method of chiral 1, 2-bis [ (2-methoxyphenyl) phenylphosphinyl ] ethane 河南工程学院 2023-11-07 — — CN disclosed
CN-111032047-B Method for producing optically active compound 多特疗法-1公司 2023-10-27 — — CN disclosed
CN-114133412-A Preparation method of chiral 1, 2-bis [ (2-methoxyphenyl) phenylphosphino ] ethane 河南工程学院 2022-03-04 — — CN disclosed
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