SCHEMBL226835

SCHEMBL226835

C1=Cc2cc3ccc([nH]3)c(-c3ccccc3)c3nc(c(-c4ccccc4)c4ccc(cc1n2)[nH]4)C=C3

nearest known ligand 0.83

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
▸ STAT3 P40763 1/20 0.83
▸ STAT1 P42224 1/20 0.83
▸ TOP1 P11387 4/20 0.47
▸ CYCS P99999 3/20 0.46
▸ TERT O14746 4/20 0.44
▸ ENPP2 Q13822 1/20 0.41
▸ ABCG2 Q9UNQ0 1/20 0.36

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
SCHEMBL29585686 1.00 STAT3 (0.83) STAT3STAT1TOP1CYCSTERT
SCHEMBL30753635 0.95 STAT3 (0.86) STAT3STAT1TOP1CYCSTERT
SCHEMBL30293296 0.95 STAT3 (0.86) STAT3STAT1TOP1CYCSTERT
SCHEMBL1224432 0.95 STAT3 (0.86) STAT3STAT1TOP1CYCSTERT
SCHEMBL31550992 0.95 STAT3 (0.86) STAT3STAT1TOP1CYCSTERT
SCHEMBL473158 0.95 STAT3 (0.86) STAT3STAT1TOP1CYCSTERT
SCHEMBL2563180 0.95 STAT3 (0.91) STAT3STAT1TOP1CYCSTERT
SCHEMBL6027584 0.94 STAT3 (0.74) STAT3STAT1TOP1CYCSTERT
SCHEMBL31324939 0.94 STAT3 (0.84) STAT3STAT1TOP1CYCSTERT
SCHEMBL1275381 0.94 STAT3 (0.84) STAT3STAT1TOP1CYCSTERT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119454945-A Ultrasonic activated carrier-free nano-drug and preparation method and application thereof 浙江大学 2025-02-18 — — CN claimed
CN-107219280-A A kind of Metalloporphyrins gas sensor element and its preparation method and application 济南大学 2017-09-29 — — CN claimed
US-6825343-B2 REFLUXING TETRACYANOETHYLENE OXIDE WITH TETRAPHENYLPORPHYRIN TO FORM (5,10,15,20-TETRAPHENYL-2,3-(3'-DICYANO)CYCLOPROPANO -2,3-CHLORIN); MACROMOLECULE INTERMEDIATES USED AS CHELATE COMPOUNDS; PHOTOSENSITIVITY UNIVERSITY OF BRITISH COLUMBIA (CA) 2004-11-30 — — US claimed
US-20040019201-A1 1,3-Dipolar cycloadditions to polypyrrolic macrocycles MACALPINE JILL KIRSTEN (US) 2004-01-29 — — US claimed
US-6620929-B1 Condensing tetracyanoethylene oxide with porphyrins to form macromolecules such as 5,10,15,20-tetraphenyl-2,3-(3'-dicyano) cyclopropano-2,3-chlorin, used for photodynamic therapy; cyclization UNIVERSITY OF BRITISH COLUMBIA (CA) 2003-09-16 — — US claimed
CN-119219645-B Preparation method of substituted diphenyl porphyrin-2-formaldehyde 湖南科技大学 2026-05-19 — — CN disclosed
CN-119899348-B Preparation method of novel photoelectric catalyst of covalent organic framework and photoelectric catalyst thereof 广东药科大学 2025-09-30 — — CN disclosed
WO-2025089384-A1 PHOTOELECTRIC CONVERSION ELEMENT AND PHOTOELECTRIC CONVERSION DEVICE キヤノン株式会社 2025-05-01 — — WO disclosed
WO-2025089409-A1 PHOTOELECTRIC CONVERSION ELEMENT, PHOTOELECTRIC CONVERSION DEVICE, MOBILE BODY, AND BUILDING MATERIAL キヤノン株式会社 2025-05-01 — — WO disclosed
WO-2025089411-A1 COMPOSITION, PREPARATION METHOD FOR COMPOSITION, AND PHOTOELECTRIC CONVERSION ELEMENT キヤノン株式会社 2025-05-01 — — WO disclosed
CN-119899348-A Preparation method of novel photoelectric catalyst of covalent organic framework and photoelectric catalyst thereof 广东药科大学 2025-04-29 — — CN disclosed
CN-119899348-A Preparation method of novel photoelectric catalyst of covalent organic framework and photoelectric catalyst thereof 广东药科大学 2025-04-29 — — CN disclosed
US-5723677-A Method for hydroperoxide decomposition using novel porphyrins synthesized from dipyrromethanes and aldehydes SUN COMPANY, INC. (R&M) (US) 1998-03-03 — — US disclosed
US-5672717-A ANTITUMOR AGENTS TREATING CANCER IOWA STATE UNIVERSITY RESEARCH FOUNDATION, INC. (US) 1997-09-30 — — US disclosed
US-5571908-A Porphyrins SUN COMPANY, INC. (R&M) (US) 1996-11-05 — — US disclosed
EP-0708768-A4 TRI-SUBSTITUTED IMIDAZOLES HAVING MULTIPLE THERAPEUTIC PROPERTIES SMITHKLINE BEECHAM CORP (US) 1996-08-21 — — EP disclosed
EP-0708768-A1 TRI-SUBSTITUTED IMIDAZOLES HAVING MULTIPLE THERAPEUTIC PROPERTIES SMITHKLINE BEECHAM CORPORATION (US) 1996-05-01 — — EP disclosed
EP-0665056-A2 Method for oxidizing alkanes using halocarbyl-substituted porphyrins synthesized from meso-halocarbyl-dipyrromethanes and aldehydes SUN COMPANY, INC. (R&M) (US) 1995-08-02 — — EP disclosed
EP-0665230-A2 Halocarbyl-substituted porphyrins and their synthesis from meso-halocarbyl-dipyrromethanes and aldehydes SUN COMPANY, INC. (R&M) (US) 1995-08-02 — — EP disclosed
WO-1995002591-A1 TRI-SUBSTITUTED IMIDAZOLES HAVING MULTIPLE THERAPEUTIC PROPERTIES SMITHKLINE BEECHAM CORPORATION (US) 1995-01-26 — — WO 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-20040019201-A1 1,3-Dipolar cycloadditions to polypyrrolic macrocycles DHPS, DDT, ADCYAP1R1 STAT3 4802/4885STAT1 4772/4885TOP1 223/4885

“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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