Indole

Indole

SCHEMBL899152

S.c1ccc2[nH]ccc2c1.c1ccc2[nH]ccc2c1

nearest known ligand 0.94

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ AHR P35869 7/20 0.94
▸ CA1 P00915 2/20 0.94
▸ CA4 P22748 2/20 0.94
▸ CA6 P23280 2/20 0.94
▸ TRPA1 O75762 1/20 0.94
▸ CA2 P00918 1/20 0.94
▸ ITGB2 P05107 1/20 0.94
▸ ICAM1 P05362 1/20 0.94
▸ ITGAL P20701 1/20 0.94
▸ ADK P55263 1/20 0.94
▸ NPC1 O15118 1/20 0.50
▸ ALDH1A1 P00352 1/20 0.46
▸ CYP2A6 P11509 3/20 0.44
▸ NR4A2 P43354 2/20 0.44
▸ CMA1 P23946 1/20 0.44
▸ F7 P08709 1/20 0.44
▸ LTA4H P09960 1/20 0.44
▸ F3 P13726 1/20 0.44
▸ PARP1 P09874 1/20 0.44
▸ TYR P14679 1/20 0.44

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
Indole SCHEMBL17515233 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL9392663 0.97 AHR (0.90) AHRCA1CA4CA6TRPA1
Indole SCHEMBL28071644 0.97 AHR (1.00) AHRCA1CA4CA6TRPA1
Indole SCHEMBL29352896 0.97 — —
Indole SCHEMBL698 0.97 — —
Indole SCHEMBL30250492 0.97 — —
Indole SCHEMBL1160186 0.97 AHR (1.00) AHRCA1CA4CA6TRPA1
Indole SCHEMBL30463845 0.97 — —
Indole SCHEMBL23886438 0.94 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL7004015 0.94 AHR (0.94) AHRCA1CA4CA6TRPA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111303117-B Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2021-09-07 — — CN claimed
CN-111303117-A Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2020-06-19 — — CN claimed
CN-113234007-B Synthesis method of 4-indolylthiobutanoic acid derivative 四川轻化工大学 2022-10-25 — — CN disclosed
CN-111303117-B Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2021-09-07 — — CN disclosed
CN-111303117-B Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2021-09-07 — — CN disclosed
CN-111303117-B Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2021-09-07 — — CN disclosed
CN-113234007-A Synthesis method of 4-indolylthiobutyric acid derivative 四川轻化工大学 2021-08-10 — — CN disclosed
EP-3180420-B1 BACTERIUM OF BACILLUS SUBTILIS SSP. SHRIRAMENSIS AND USES THEREOF DCM SHRIRAM LTD (IN) 2020-10-21 — — EP disclosed
CN-111303117-A Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2020-06-19 — — CN disclosed
CN-111303117-A Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2020-06-19 — — CN disclosed
CN-111303117-A Preparation method of nitrogen heterocyclic ring substituted indole thioether compound 常州工程职业技术学院 2020-06-19 — — CN disclosed
US-6916841-B2 Inhibitors of phospholipase enzymes GENETICS INSTITUTE, LLC (US) 2005-07-12 — — US disclosed
US-6828344-B1 Direct inhibition of the activity of phospholipase A2 has been suggested as a useful mechanism for a therapeutic agent for inflammation GENETICS INSTITUTE, LLC 2004-12-07 — — US disclosed
US-20030153751-A1 Inhibitors of phospholipase enzymes AMERICAN HOME PRODUCTS CORPORATION 2003-08-14 — — US disclosed
US-6500853-B1 ENZYME INHIBITORS SUCH AS 4-((1-BENZHYDRYL-5-(((BUTYLAMINO)-CARBONYL)AMINO)-1H-INDOL-3-YL)METHYL)-3 -METHOXYBENZOIC ACID USED AS ANTIINFLAMMATORY AGENTS FOR PROPHYLAXIS OF ARTHRITIS, INFLAMMATORY BOWEL DISEASE OR ASTHMA GENETICS INSTITUTE, LLC 2002-12-31 — — US disclosed
EP-1062205-A2 INHIBITORS OF PHOSPHOLIPASE ENZYMES GENETICS INSTITUTE, INC. (US) 2000-12-27 — — EP disclosed
EP-1056719-A2 INHIBITORS OF PHOSPHOLIPASE ENZYMES GENETICS INSTITUTE, INC. (US) 2000-12-06 — — EP disclosed
WO-1999043654-A2 INHIBITORS OF PHOSPHOLIPASE ENZYMES GENETICS INSTITUTE, INC. (US) 1999-09-02 — — WO disclosed
WO-1999043651-A2 INHIBITORS OF PHOSPHOLIPASE ENZYMES GENETICS INSTITUTE, INC. (US) 1999-09-02 — — WO disclosed
US-5059444-A Dispersing red pigment; heating to discolor and sterilize ITO HAM KABUSHIKI KAISHA (JP) 1991-10-22 — — 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 (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-20030153751-A1 Inhibitors of phospholipase enzymes PLA2G4C, PLA2G4B, PLA2G4A AHR 4427/4885CA1 1996/4885CA4 2960/4885

“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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