SCHEMBL9007697

SCHEMBL9007697

PC(c1ccccc1)(c1ccccc1)C1C2CCC(C2)C1C(P)(c1ccccc1)c1ccccc1

nearest known ligand 0.35

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.33
CHRM3 P20309 3/20 0.33
CYP2D6 P10635 2/20 0.32
MEN1 O00255 1/20 0.32
HRH1 P35367 1/20 0.32
SCN1A P35498 1/20 0.32
KMT2A Q03164 1/20 0.32
SCN2A Q99250 1/20 0.32
SCN3A Q9NY46 1/20 0.32
MAPK1 P28482 2/20 0.32
CHRM2 P08172 2/20 0.32
CHRM1 P11229 2/20 0.32
KEAP1 Q14145 1/20 0.32
NFE2L2 Q16236 1/20 0.32
ALDH1A1 P00352 4/20 0.31
TSHR P16473 2/20 0.31
HPGD P15428 2/20 0.31
KCNN4 O15554 1/20 0.31
MC4R P32245 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31

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
SCHEMBL11435348 1.00 LMNA (0.33) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL8608891 0.80 HTR2C (0.38) ALDH1A1TSHR
SCHEMBL5175216 0.78 MAPK1 (0.34) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL749097 0.75 KCNN4 (0.38) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL3502282 0.75 KCNN4 (0.38) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL11328095 0.75 KCNN4 (0.38) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL10907499 0.73 CYP2D6 (0.41) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL2464761 0.73 CYP2D6 (0.36) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL18788591 0.73 CYP2D6 (0.41) LMNACHRM3CYP2D6MEN1HRH1
SCHEMBL8607528 0.72 CHRM3 (0.33) CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4216331-A Use of chiral rhodium-diphosphine catalyst capable of catalytic reduction of a tetramisole precursor to give a significant excess of the desired S-(-) isomer levamisole AMERICAN CYANAMID COMPANY (US) 1980-08-05 US claimed
US-4166824-A Chiral rhodium-diphosphine catalyst capable of catalytic reduction of a tetramisole precursor to give a significant excess of the desired S-(-)isomer, levamisole AMERICAN CYANAMID COMPANY (US) 1979-09-04 US claimed
JP-55100331-A None JP disclosed
US-5530162-A Process for the hydrogenation of aryl phosphines and products obtained therefrom RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1996-06-25 US disclosed
US-4370258-A PLATINUM CATALYST, INB METAL HALIDE ASSISTANT CATALYST AND BIDENTATE LIGAND PROMOTER AGENCY OF INDUSTRIAL SCIENCE & TECHNOLOGY (JP) 1983-01-25 US disclosed
US-4283563-A HYDROFORMYLATION OF OLEFINS USING A PLATINUM-PHOSPHINE COMPLEX CATALYST AGENCY OF INDUSTRIAL SCIENCE & TECHNOLOGY (JP) 1981-08-11 US disclosed
US-4229381-A HYDROFORMYLATION OF OLEFINS; PLATINUM CATALYST; BIDENTATE LIGAND AGENCY OF INDUSTRIAL SCIENCE & TECHNOLOGY (JP) 1980-10-21 US disclosed
US-4216331-A Use of chiral rhodium-diphosphine catalyst capable of catalytic reduction of a tetramisole precursor to give a significant excess of the desired S-(-) isomer levamisole AMERICAN CYANAMID COMPANY (US) 1980-08-05 US disclosed
JP-S55100331-A PREPARATION OF ALDEHYDE AGENCY OF IND SCIENCE & TECHNOL 1980-07-31 JP disclosed
US-4166824-A Chiral rhodium-diphosphine catalyst capable of catalytic reduction of a tetramisole precursor to give a significant excess of the desired S-(-)isomer, levamisole AMERICAN CYANAMID COMPANY (US) 1979-09-04 US disclosed