SCHEMBL946372

SCHEMBL946372

Cc1ccc(S(=O)(=O)n2cc(C=O)c3ccccc32)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 1/20 1.00
▸ UBE2N P61088 1/20 1.00
▸ L3MBTL1 Q9Y468 2/20 0.64
▸ CA2 P00918 1/20 0.61
▸ CA9 Q16790 1/20 0.61
▸ HTR6 P50406 7/20 0.60
▸ ALOX5 P09917 3/20 0.53
▸ ALK Q9UM73 1/20 0.53
▸ CYP19A1 P11511 2/20 0.52
▸ KLK7 P49862 1/20 0.52
▸ ALDH1A1 P00352 1/20 0.51
▸ IMPDH2 P12268 1/20 0.51
▸ PTGS2 P35354 1/20 0.51
▸ POLB P06746 1/20 0.50
▸ ALDH3A1 P30838 1/20 0.50
▸ HTT P42858 1/20 0.50
▸ NOD1 Q9Y239 1/20 0.50

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
SCHEMBL29694480 1.00 KDM4E (1.00) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL29576861 0.89 KDM4E (0.81) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL723339 0.89 KDM4E (0.81) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL16291995 0.89 KDM4E (0.80) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL31262899 0.89 KDM4E (0.80) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL30542061 0.87 KDM4E (0.77) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL946340 0.87 KDM4E (0.77) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL946492 0.87 KDM4E (0.77) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL14735529 0.87 KDM4E (0.77) KDM4EUBE2NL3MBTL1CA2CA9
SCHEMBL946643 0.86 KDM4E (0.76) KDM4EUBE2NL3MBTL1CA2CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117024326-A 5-amino substituted indole compound, preparation method thereof and application thereof in anti-acetylcholinesterase medicine 平顶山学院 2023-11-10 — — CN claimed
CN-116693500-A Quinolinone derivative containing sulfonyl substituted indolyl acylhydrazone structure on 3-position nitrogen atom, and preparation method and application thereof 太原理工大学 2023-09-05 — — CN claimed
CN-116693503-A Quinolinone derivative containing sulfonyl substituted indolyl acylhydrazone structure on 1-position nitrogen atom, and preparation method and application thereof 太原理工大学 2023-09-05 — — CN claimed
WO-2025064829-A1 A MOLECULAR SCAFFOLD FOR DEPLETING HRPN13 AND A SELECT GROUP OF KEN BOX PROTEINS THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2025-03-27 — — WO disclosed
CN-114716289-B Preparation method of chiral benzyl alcohol derivative 华中师范大学 2024-03-01 — — CN disclosed
CN-117024326-A 5-amino substituted indole compound, preparation method thereof and application thereof in anti-acetylcholinesterase medicine 平顶山学院 2023-11-10 — — CN disclosed
CN-116693503-A Quinolinone derivative containing sulfonyl substituted indolyl acylhydrazone structure on 1-position nitrogen atom, and preparation method and application thereof 太原理工大学 2023-09-05 — — CN disclosed
CN-116693500-A Quinolinone derivative containing sulfonyl substituted indolyl acylhydrazone structure on 3-position nitrogen atom, and preparation method and application thereof 太原理工大学 2023-09-05 — — CN disclosed
CN-114716289-A Preparation method of chiral benzyl alcohol derivative 华中师范大学 2022-07-08 — — CN disclosed
CN-112028812-B 4-bromoindole compound and preparation method thereof 平顶山学院 2022-03-22 — — CN disclosed
CN-112028813-B 4-chloro indole compound and preparation method thereof 平顶山学院 2022-03-22 — — CN disclosed
US-6207679-B1 FOR INHIBITING GROWTH OF BACTERIAL MICROORGANISMS SEPRACOR, INC. 2001-03-27 — — US disclosed
WO-2001019816-A1 NOVEL SPIROHETEROCYCLIC COMPOUNDS USEFUL AS REVERSIBLE INHIBITORS OF CYSTEINE PROTEASES BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2001-03-22 — — WO disclosed
WO-2001009110-A1 NOVEL SUCCINATE DERIVATIVE COMPOUNDS USEFUL AS CYSTEINE PROTEASE INHIBITORS BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2001-02-08 — — WO disclosed
US-6172084-B1 BACTERICIDES AGAINST ANTIBIOTIC RESISTANT STRAINS OF STAPHYLOCOCCUS, STREPTOCOCCUS AND ENTEROCOCCUS SEPRACOR, INC. 2001-01-09 — — US disclosed
US-6103905-A EFFECTIVE AGAINST DRUG RESISTANT GRAMPOSITIVE BACTERIAL INFECTIONS; ANTIBIOTICS SEPRACOR, INC. (US) 2000-08-15 — — US disclosed
WO-2000034265-A2 QUINOLINE-INDOLE ANTIMICROBIAL AGENTS SEPRACOR, INC. (US) 2000-06-15 — — WO disclosed
EP-0991623-A2 QUINOLINE-INDOLE ANTIMICROBIAL AGENTS, USES AND COMPOSITIONS RELATED THERETO SEPRACOR, INC. (US) 2000-04-12 — — EP disclosed
WO-1998057931-A2 QUINOLINE-INDOLE ANTIMICROBIAL AGENTS, USES AND COMPOSITIONS RELATED THERETO SEPRACOR INC. (US) 1998-12-23 — — WO disclosed
EP-0185538-A2 The synthesis of indole alkaloids Kong, Yun Cheung, Dr. (HK) 1986-06-25 — — EP disclosed
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