SCHEMBL1304675

SCHEMBL1304675

B.c1ccc(-c2ccc(Pc3ccc(-c4ccccc4)cc3)cc2)cc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.53
MMP3 P08254 1/20 0.52
BCL2L1 Q07817 1/20 0.52
TAAR1 Q96RJ0 2/20 0.46
CYP1A2 P05177 2/20 0.46
MAPK1 P28482 1/20 0.46
CYP3A4 P08684 1/20 0.46
HSD17B10 Q99714 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
CA1 P00915 2/20 0.40
CA2 P00918 2/20 0.40
MGLL Q99685 1/20 0.40
KIF11 P52732 1/20 0.40
NOTUM Q6P988 1/20 0.39
ALOX5 P09917 1/20 0.39
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
CYP1A1 P04798 1/20 0.37
CYP1B1 Q16678 1/20 0.37
CA12 O43570 1/20 0.37

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
SCHEMBL5414256 0.97 ALDH1A1 (0.56) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
SCHEMBL28449419 0.94 ALDH1A1 (0.53) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
SCHEMBL21538257 0.91 MMP3 (0.48) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
Biphenyl SCHEMBL10535523 0.88 ALDH1A1 (0.60) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
Biphenyl SCHEMBL27082161 0.88 ALDH1A1 (0.60) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
Biphenyl SCHEMBL7871107 0.85 ALDH1A1 (0.56) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
Biphenyl SCHEMBL7877163 0.85 ALDH1A1 (0.56) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
Biphenyl SCHEMBL4388996 0.85 ALDH1A1 (0.56) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
Biphenyl SCHEMBL7868148 0.85 ALDH1A1 (0.56) ALDH1A1MMP3BCL2L1TAAR1CYP1A2
Butane SCHEMBL27676924 0.85 MMP3 (0.44) ALDH1A1MMP3BCL2L1TAAR1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8053604-B2 Process for preparation of diphosphine compounds and intermediates for the process TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2011-11-08 US disclosed
US-20100125153-A1 PROCESS FOR PREPARATION OF DIPHOSPHINE COMPOUNDS AND INTERMEDIATES FOR THE PROCESS SPERA PHARMA, INC. (JP) 2010-05-20 US disclosed
US-7678942-B2 Process for preparation of diphosphine compounds and intermediates for the process TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-03-16 US disclosed
EP-1452537-B1 PROCESS FOR PREPARATION OF DIPHOSPHINE COMPOUNDS AND INTERMEDIATES FOR THE PROCESS TAKEDA PHARMACEUTICAL (JP) 2009-08-05 EP disclosed
US-20070161805-A1 Phosphine-borane complex enantiomorph compounds produced in solvents and in the presence of nickel catalysts; useful for asymmetric synthesis of compounds useful as drug for prophylaxis or treatment of increased urinary frequency or urinary incontinence, Alzheimer's disease SPERA PHARMA, INC. (JP) 2007-07-12 US disclosed
US-7208633-B2 Process for preparation of diphosphine compounds and intermediates for the process TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2007-04-24 US disclosed
US-20050027124-A1 Process for preparation of diphosphine compounds and intermediates for the process SPERA PHARMA, INC. (JP) 2005-02-03 US disclosed
EP-1452537-A1 PROCESS FOR PREPARATION OF DIPHOSPHINE COMPOUNDS AND INTERMEDIATES FOR THE PROCESS Takeda Chemical Industries, Ltd. (JP) 2004-09-01 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100125153-A1 PROCESS FOR PREPARATION OF DIPHOSPHINE COMPOUNDS AND INTERMEDIATES FOR THE PROCESS H1-10, ITPA, RER1 ALDH1A1 4580/4885MMP3 4858/4885BCL2L1 4452/4885
US-20070161805-A1 Phosphine-borane complex enantiomorph compounds produced in solvents and in the presence of nickel catalysts; useful for asymmetric synthesis of compounds useful as drug for prophylaxis or treatment of increased urinary frequency or urinary incontinence, Alzheimer's disease BACE1, H1-10, PRMT1 ALDH1A1 2206/4885MMP3 3394/4885BCL2L1 2625/4885
US-20050027124-A1 Process for preparation of diphosphine compounds and intermediates for the process H1-10, ITPA, RER1 ALDH1A1 4580/4885MMP3 4858/4885BCL2L1 4459/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.