SCHEMBL12880845

SCHEMBL12880845

Cc1cc(P(c2ccccc2)c2ccccc2)c(-c2c(C)cc(C(F)(F)F)cc2P(c2ccccc2)c2ccccc2)c(C)c1C

nearest known ligand 0.32

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.32
TSHR P16473 1/20 0.32
MAPT P10636 1/20 0.32
DRD1 P21728 2/20 0.31
CYP3A4 P08684 1/20 0.31
TDP1 Q9NUW8 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
SCHEMBL19009982 0.91 ALDH1A1 (0.39) ALDH1A1TSHRMAPTDRD1CYP3A4
SCHEMBL12446368 0.84 CYP3A4 (0.42) ALDH1A1MAPTDRD1CYP3A4TDP1
SCHEMBL29597288 0.84 CYP3A4 (0.42) ALDH1A1MAPTDRD1CYP3A4TDP1
SCHEMBL17426096 0.83 CYP3A4 (0.38) DRD1CYP3A4TDP1
SCHEMBL31566348 0.77 HSD11B1 (0.30)
SCHEMBL1043812 0.77 HSD11B1 (0.30)
SCHEMBL13177945 0.76 CYP3A4 (0.34) DRD1CYP3A4TDP1
SCHEMBL7024931 0.76 ESR1 (0.36) ALDH1A1MAPTDRD1CYP3A4TDP1
SCHEMBL4205832 0.75 ALDH1A1 (0.39) ALDH1A1TSHRDRD1CYP3A4TDP1
SCHEMBL3115547 0.72 DPP4 (0.41) CYP3A4TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180186725-A1 METHOD FOR THE HOMOGENEOUS CATALYTIC REDUCTIVE AMINATION OF CARBONYL COMPOUNDS BASF SE (DE) 2018-07-05 US disclosed
US-9975837-B2 Method for synthesizing optically active carbonyl compounds BASF SE (DE) 2018-05-22 US disclosed
US-20180057437-A1 METHOD FOR SYNTHESIZING OPTICALLY ACTIVE CARBONYL COMPOUNDS BASF SE (DE) 2018-03-01 US disclosed
US-20170173572-A1 CHIRAL LIGAND-BASED METAL-ORGANIC FRAMEWORKS FOR BROAD-SCOPE ASYMMETRIC CATALYSIS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2017-06-22 US disclosed
US-8623621-B2 Method for producing optically active 2-methyl-alkanols BASF SE (DE) 2014-01-07 US disclosed
US-20110045560-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE 2-METHYL-ALKANOLS BASF AKTIENGESELLSCHAFT (DE) 2011-02-24 US 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-20170173572-A1 CHIRAL LIGAND-BASED METAL-ORGANIC FRAMEWORKS FOR BROAD-SCOPE ASYMMETRIC CATALYSIS POF1B, FGFR1, COASY ALDH1A1 861/4885TSHR 2334/4885MAPT 4198/4885
US-20180186725-A1 METHOD FOR THE HOMOGENEOUS CATALYTIC REDUCTIVE AMINATION OF CARBONYL COMPOUNDS CAT, AOC1, CYCS ALDH1A1 553/4885TSHR 3414/4885MAPT 3635/4885
US-20180057437-A1 METHOD FOR SYNTHESIZING OPTICALLY ACTIVE CARBONYL COMPOUNDS CBR3, CBR1, HRH4 ALDH1A1 653/4885TSHR 188/4885MAPT 4602/4885

“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.