SCHEMBL5015413

SCHEMBL5015413

FC(F)(F)c1ccc(-c2c3nc(c(-c4c(Br)cccc4Br)c4ccc([nH]4)c(-c4ccc(C(F)(F)F)cc4)c4nc(c(-c5c(Br)cccc5Br)c5ccc2[nH]5)C=C4)C=C3)cc1

nearest known ligand 0.47

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
▸ TOP1 P11387 4/20 0.46
▸ CYCS P99999 3/20 0.44
▸ ENPP2 Q13822 1/20 0.43
▸ TERT O14746 4/20 0.43
▸ ABCG2 Q9UNQ0 1/20 0.38

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
SCHEMBL15085693 0.87 TOP1 (0.56) TOP1CYCSENPP2TERTABCG2
SCHEMBL5011966 0.87 TERT (0.46) TOP1CYCSENPP2TERTABCG2
Hydrochloric Acid SCHEMBL31547368 0.84 TOP1 (0.57) TOP1CYCSENPP2TERTABCG2
SCHEMBL5013893 0.83 TOP1 (0.51) TOP1CYCSENPP2TERT
SCHEMBL16604343 0.82 TOP1 (0.51) TOP1CYCSENPP2TERT
SCHEMBL16921240 0.81 TOP1 (0.50) TOP1CYCSENPP2TERTABCG2
SCHEMBL1792646 0.78 TERT (0.42) TOP1CYCSENPP2TERT
SCHEMBL5013908 0.77 TERT (0.39) TOP1CYCSENPP2TERT
SCHEMBL5013772 0.77 TOP1 (0.59) TOP1CYCSENPP2TERTABCG2
SCHEMBL8908238 0.76 TERT (0.46) TOP1CYCSTERT

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-7417142-B2 Chiral porphyrins, chiral metalloporphyrins, and methods for synthesis of the same THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION, INC. (US) 2008-08-26 — — US disclosed
US-7417142-B2 Chiral porphyrins, chiral metalloporphyrins, and methods for synthesis of the same THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION, INC. (US) 2008-08-26 — — US disclosed
US-7417142-B2 Chiral porphyrins, chiral metalloporphyrins, and methods for synthesis of the same THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION, INC. (US) 2008-08-26 — — US disclosed
US-20060030718-A1 Cobalt-based catalysts for the cyclization of alkenes UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2006-02-09 — — US disclosed
US-20050124596-A1 Chiral porphyrins, chiral metalloporphyrins, and methods for synthesis of the same UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2005-06-09 — — 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 (2 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-20060030718-A1 Cobalt-based catalysts for the cyclization of alkenes PPOX, HCCS, ICOSLG TOP1 1268/4885CYCS 6/4885ENPP2 3182/4885
US-20050124596-A1 Chiral porphyrins, chiral metalloporphyrins, and methods for synthesis of the same PPOX, PPIF, HMBS TOP1 1564/4885CYCS 57/4885ENPP2 1786/4885

“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.

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