SCHEMBL3544102

SCHEMBL3544102

COc1cc2c(cc1OC)C(Cc1ccc(-c3ccc(F)cc3)cc1)(OC(=O)C(=O)OC1(Cc3ccc(-c4ccc(F)cc4)cc3)NCCc3cc(OC)c(OC)cc31)NCC2

nearest known ligand 0.42

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ABCB1 P08183 6/20 0.42
KMT2A Q03164 4/20 0.37
KDM4C Q9H3R0 1/20 0.36
LMNA P02545 1/20 0.36
MAPK1 P28482 1/20 0.36
HTT P42858 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
MLNR O43193 1/20 0.35
CYP2D6 P10635 1/20 0.35
ABCC1 P33527 1/20 0.35
ATM Q13315 1/20 0.35
KCNH2 Q12809 1/20 0.34
TMEM97 Q5BJF2 1/20 0.34
SIGMAR1 Q99720 1/20 0.34
TRPV1 Q8NER1 1/20 0.34
MEN1 O00255 1/20 0.34
POLB P06746 1/20 0.34

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
SCHEMBL5090771 0.91 KMT2A (0.40) ABCB1KMT2ALMNAABCC1MEN1
SCHEMBL3548729 0.91 ABCB1 (0.36) ABCB1LMNANPSR1ABCC1
SCHEMBL3546929 0.86 HCRTR1 (0.40) ABCB1KMT2AHTTMEN1
SCHEMBL3548501 0.83 CFD (0.37) ABCB1KMT2AMEN1
SCHEMBL3543083 0.80 ACHE (0.36) ABCB1KMT2AMEN1POLB
SCHEMBL5094562 0.79 CYP26A1 (0.37) KMT2ALMNAHTTNPSR1MEN1
SCHEMBL3778768 0.72 LDHA (0.35) KMT2ALMNAHTTNPSR1MEN1
SCHEMBL2794818 0.72 LDHA (0.35) KMT2ALMNAHTTNPSR1MEN1
SCHEMBL3631986 0.72 KMT2A (0.37) KMT2ALMNAMAPK1HTTNPSR1
SCHEMBL2798586 0.71 ALDH1A1 (0.32) KMT2ALMNAHTTNPSR1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7718672-B2 Substituted tetrahydroisoquinoline compounds, methods of making, and their use UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2010-05-18 US disclosed
US-20080033007-A1 Substituted Tetrahydroisoquinoline Compounds for Cancer Therapy MILLER DUANE D 2008-02-07 US disclosed
US-20070270460-A1 SUBSTITUTED TETRAHYDROISOQUINOLINE COMPOUNDS, METHODS OF MAKING, AND THEIR USE MILLER DUANE D 2007-11-22 US disclosed
US-7241774-B2 Substituted tetrahydroisoquinoline compounds, methods of making, and their use UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2007-07-10 US disclosed
US-20040019078-A1 Substituted tetrahydroisoquinoline compounds, methods of making, and their use UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION,THE 2004-01-29 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-20080033007-A1 Substituted Tetrahydroisoquinoline Compounds for Cancer Therapy BAD, TP53, MCL1 ABCB1 556/4885KMT2A 1046/4885KDM4C 1680/4885
US-20070270460-A1 SUBSTITUTED TETRAHYDROISOQUINOLINE COMPOUNDS, METHODS OF MAKING, AND THEIR USE BAX, CASP3, BAD ABCB1 67/4885KMT2A 1317/4885KDM4C 720/4885
US-20040019078-A1 Substituted tetrahydroisoquinoline compounds, methods of making, and their use BAD, BAX, CASP3 ABCB1 61/4885KMT2A 641/4885KDM4C 263/4885

“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.