SCHEMBL8909182

SCHEMBL8909182

COc1cccc(P(=O)(Oc2ccccc2)Oc2ccccc2)c1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 2/20 0.66
▸ TDP1 Q9NUW8 2/20 0.66
▸ LMNA P02545 2/20 0.55
▸ HCRTR1 O43613 1/20 0.51
▸ PKM P14618 1/20 0.50
▸ HTT P42858 1/20 0.50
▸ CA4 P22748 4/20 0.49
▸ CA12 O43570 3/20 0.49
▸ CA1 P00915 3/20 0.49
▸ CA2 P00918 3/20 0.49
▸ CA5A P35218 3/20 0.49
▸ CA7 P43166 3/20 0.49
▸ CA9 Q16790 3/20 0.49
▸ CA5B Q9Y2D0 3/20 0.49
▸ NPC1 O15118 4/20 0.46
▸ RAB9A P51151 4/20 0.46
▸ SMN1; SMN2 Q16637 1/20 0.44
▸ NLRP3 Q96P20 1/20 0.44
▸ HPGD P15428 1/20 0.44
▸ MEN1 O00255 2/20 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
SCHEMBL29034878 0.83 TDP1 (0.73) L3MBTL1TDP1PKMHTTCA4
SCHEMBL12230072 0.83 ACHE (0.47) L3MBTL1TDP1LMNAHCRTR1PKM
SCHEMBL28101003 0.81 TDP1 (0.70) L3MBTL1TDP1LMNAPKMHTT
SCHEMBL7619840 0.81 LMNA (0.50) L3MBTL1LMNAHCRTR1PKMHTT
SCHEMBL561190 0.80 L3MBTL1 (1.00) L3MBTL1TDP1LMNAPKMHTT
SCHEMBL29968685 0.79 ACHE (0.50) L3MBTL1LMNAHCRTR1CA1CA2
SCHEMBL8163505 0.79 ACHE (0.50) L3MBTL1LMNAHCRTR1CA1CA2
SCHEMBL28388783 0.79 HCRTR1 (0.59) L3MBTL1TDP1LMNAHCRTR1PKM
SCHEMBL28834594 0.79 L3MBTL1 (0.66) L3MBTL1TDP1LMNAHTTCA4
SCHEMBL27988575 0.79 TDP1 (0.66) L3MBTL1TDP1LMNAHTTCA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5600015-A USING RUTHENIUM COMPLEX OF OPTICALLY ACTIVE ATROPISOMERIC DIPHOSPHINE LIGAND AS HYDROGENATION CATALYST HOFFMANN-LA ROCHE INC. (US) 1997-02-04 — — US disclosed
EP-0565975-B1 Process for the preparation of isoprenoid derivatives HOFFMANN LA ROCHE (CH) 1996-09-04 — — EP disclosed
EP-0530335-B1 DIPHOSPHONIC ACID DERIVATES AS INTERMEDIATES FOR THE PRODUCTION OF DIPHOSPHINE LIGANDS HOFFMANN LA ROCHE (CH) 1996-08-14 — — EP disclosed
EP-0530336-B1 CHIRAL PHOSPHINES HOFFMANN LA ROCHE (CH) 1996-03-06 — — EP disclosed
US-5302738-A Chiral phosphines HOFFMANN-LA ROCHE INC. (US) 1994-04-12 — — US disclosed
US-5274125-A Chirale phosphines HOFFMANN-LA ROCHE INC. (US) 1993-12-28 — — US disclosed
EP-0565975-A2 Process for the preparation of isoprenoid derivatives F. HOFFMANN-LA ROCHE AG (CH) 1993-10-20 — — EP disclosed
EP-0530335-A1 DIPHOSPHONIC ACID DERIVATES AS INTERMEDIATES FOR THE PRODUCTION OF DIPHOSPHINE LIGANDS. HOFFMANN LA ROCHE (CH) 1993-03-10 — — EP disclosed
EP-0530336-A1 CHIRAL PHOSPHINES. HOFFMANN LA ROCHE (CH) 1993-03-10 — — EP disclosed
WO-1992016536-A1 CHIRAL PHOSPHINES F. HOFFMANN-LA ROCHE AG (CH) 1992-10-01 — — WO disclosed
WO-1992016535-A1 DIPHOSPHONIC ACID DERIVATES AS INTERMEDIATES FOR THE PRODUCTION OF DIPHOSPHINE LIGANDS F.HOFFMANN-LA ROCHE AG (CH) 1992-10-01 — — WO disclosed
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