SCHEMBL352668

SCHEMBL352668

O=Cc1cc2cc3nc(cc4ccc(cc5nc(cc1[nH]2)C=C5)[nH]4)C=C3

nearest known ligand 0.37

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
▸ STAT3 P40763 1/20 0.37
▸ STAT1 P42224 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
SCHEMBL28676277 0.98 STAT3 (0.36) STAT3STAT1
SCHEMBL19490351 0.93 GRIA1 (0.32) STAT3STAT1
SCHEMBL6566436 0.90 STAT3 (0.32) STAT3STAT1
SCHEMBL461737 0.83 STAT3 (0.37) STAT3STAT1
SCHEMBL27728578 0.82 STAT3 (0.36) STAT3STAT1
SCHEMBL2752554 0.79 STAT3 (0.36) STAT3STAT1
Formic Acid SCHEMBL27490312 0.78 STAT3 (0.36) STAT3STAT1
SCHEMBL29267780 0.78 STAT3 (0.36) STAT3STAT1
SCHEMBL9866324 0.78 STAT3 (0.49) STAT3STAT1
SCHEMBL38329 0.78 STAT3 (0.49) STAT3STAT1

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 39 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1353925-A2 PROCESSES FOR LARGE SCALE PRODUCTION OF TETRAPYRROLES Miravant Pharmaceuticals, Inc. (US) 2003-10-22 — — EP claimed
WO-2002083686-A2 PROCESSES FOR LARGE SCALE PRODUCTION OF TETRAPYRROLES MIRAVANT PHARMACEUTICALS, INC. (US) 2002-10-24 — — WO claimed
JP-7330773-A — — None — — JP disclosed
JP-3284681-A — — None — — JP disclosed
CN-119219645-B Preparation method of substituted diphenyl porphyrin-2-formaldehyde 湖南科技大学 2026-05-19 — — CN disclosed
CN-119219645-B Preparation method of substituted diphenyl porphyrin-2-formaldehyde 湖南科技大学 2026-05-19 — — CN disclosed
CN-119219645-A Preparation method of substituted diphenyl porphyrin-2-formaldehyde 湖南科技大学 2024-12-31 — — CN disclosed
CN-119219645-A Preparation method of substituted diphenyl porphyrin-2-formaldehyde 湖南科技大学 2024-12-31 — — CN disclosed
US-8952357-B2 Cytochrome c552 color imaging element and method of manufacturing the same, cytochrome c552 photosensor and method of manufacturing the same, cytochrome c552 photoelectric transducer and method of manufacturing the same, and cytochrome c552 electronic device SONY CORPORATION (JP) 2015-02-10 — — US disclosed
CN-102318065-B Color imaging element and method for manufacturing the same, optical sensor and method for manufacturing the same, photoelectric transducer and method for manufacturing the same, and electronic device SONY CORP 2013-11-27 — — CN disclosed
CN-103367642-A Color imaging element and method of manufacturing the same, photosensor and method of manufacturing the same, and photoelectric transducer and method of manufacturing the same SONY CORP 2013-10-23 — — CN disclosed
US-20060183145-A1 Use of reversible extension terminator in nucleic acid sequencing PACIFIC BIOSCIENCES OF CALIFORNIA, INC. 2006-08-17 — — US disclosed
WO-2006083751-A2 USE OF REVERSIBLE EXTENSION TERMINATOR IN NUCLEIC ACID SEQUENCING PACIFIC BIOSCIENCES OF CALIFORNIA, INC. (US) 2006-08-10 — — WO disclosed
WO-2006038823-A1 BETA-SUBSTITUTED PORPHYRINS MASSEY UNIVERSITY (NZ) 2006-04-13 — — WO disclosed
US-20050277770-A1 condensing a 5-acetaldipyrromethane with a dipyrromethane-1,9-dicarbinol to produce a porphyrin having an acetal group substituted thereon at the 5 position; and then hydrolyzing said porphyrin to produce said 5-formylporphyrin NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2005-12-15 — — US disclosed
US-20050277770-A1 condensing a 5-acetaldipyrromethane with a dipyrromethane-1,9-dicarbinol to produce a porphyrin having an acetal group substituted thereon at the 5 position; and then hydrolyzing said porphyrin to produce said 5-formylporphyrin NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2005-12-15 — — US disclosed
EP-1353925-A2 PROCESSES FOR LARGE SCALE PRODUCTION OF TETRAPYRROLES Miravant Pharmaceuticals, Inc. (US) 2003-10-22 — — EP disclosed
WO-2002083686-A2 PROCESSES FOR LARGE SCALE PRODUCTION OF TETRAPYRROLES MIRAVANT PHARMACEUTICALS, INC. (US) 2002-10-24 — — WO disclosed
JP-H07330773-A PORPHYRIN DERIVATIVE AND ITS USE TOYO HATSUKA KOGYO KK 1995-12-19 — — JP disclosed
JP-H03284681-A PORPHYRIN DERIVATIVE TOYO HATSUKA KOGYO KK 1991-12-16 — — JP 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-20050277770-A1 condensing a 5-acetaldipyrromethane with a dipyrromethane-1,9-dicarbinol to produce a porphyrin having an acetal group substituted thereon at the 5 position; and then hydrolyzing said porphyrin to produce said 5-formylporphyrin DHPS, NOTUM, DOHH STAT3 4298/4885STAT1 4505/4885

“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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