SCHEMBL2963039

SCHEMBL2963039

C1=Cc2cc3ccc([nH]3)c(-c3ncc[nH]3)c3nc(c(-c4ncc[nH]4)c4ccc(cc1n2)[nH]4)C=C3

nearest known ligand 0.50

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ STAT3 P40763 1/20 0.50
▸ STAT1 P42224 1/20 0.50
▸ CYCS P99999 1/20 0.34
▸ TOP1 P11387 1/20 0.33
▸ TERT O14746 4/20 0.33
▸ MTOR P42345 1/20 0.33
▸ ADK P55263 1/20 0.33
▸ NISCH Q9Y2I1 1/20 0.33
▸ IDO1 P14902 1/20 0.32

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
SCHEMBL2955031 0.96 STAT3 (0.52) STAT3STAT1CYCSTOP1MTOR
SCHEMBL3520923 0.89 STAT3 (0.42) STAT3STAT1TERT
SCHEMBL4732325 0.85 TOP1 (0.43) CYCSTOP1TERTMTORADK
SCHEMBL2963034 0.82 NISCH (0.36) STAT3STAT1MTORADKNISCH
SCHEMBL9582368 0.78 STAT3 (0.57) STAT3STAT1MTOR
SCHEMBL2955029 0.77 IDO1 (0.36) STAT3STAT1MTORADKNISCH
SCHEMBL18343621 0.77 STAT3 (0.55) STAT3STAT1CYCSTOP1TERT
SCHEMBL2962139 0.76 IDO1 (0.35) STAT3STAT1MTORADKNISCH
SCHEMBL226835 0.75 STAT3 (0.83) STAT3STAT1CYCSTOP1TERT
SCHEMBL29585686 0.75 STAT3 (0.83) STAT3STAT1CYCSTOP1TERT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1690865-B1 PORPHYRIN/PHTHALOCYANINE DIMER AND TETRAMER DIRECTLY BONDED AT PI SYSTEM AND PROCESSES FOR PRODUCING THESE NAT UNIV CORP NARA INST (JP) 2012-09-05 — — EP disclosed
US-7767808-B2 for photoelectric conversion elements National University Corporation NARA Institute of Science and Technology (JP) 2010-08-03 — — US disclosed
US-20060217538-A1 Porphyrin-phthalocyanine dimer and tetramer having directly-bound Pi electron systems and production method thereof NATIONAL UNIVERSITY CORPORATION, NARA INSTITUTE OF SCIENCE AND TECHNOLOGY (JP) 2006-09-28 — — US disclosed
EP-1690865-A1 PORPHYRIN/PHTHALOCYANINE DIMER AND TETRAMER DIRECTLY BONDED AT PI SYSTEM AND PROCESSES FOR PRODUCING THESE National University Corporation Nara Institute of Science and Technology (JP) 2006-08-16 — — 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 (1 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-20060217538-A1 Porphyrin-phthalocyanine dimer and tetramer having directly-bound Pi electron systems and production method thereof CYC1, RRP12, PPOX STAT3 2160/4885STAT1 2354/4885CYCS 66/4885

“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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