SCHEMBL233322

SCHEMBL233322

Cn1ccc2ccc(C(=O)O)cc21

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 1/20 0.51
MAPK11 Q15759 1/20 0.50
MAPK14 Q16539 1/20 0.50
CHRNA7 P36544 1/20 0.49
MCL1 Q07820 1/20 0.47
KDM2B Q8NHM5 1/20 0.46
GPR183 P32249 1/20 0.45
KDM4E B2RXH2 3/20 0.44
HCAR3 P49019 1/20 0.44
SCN9A Q15858 1/20 0.43
TUBB4A P04350 1/20 0.42
TUBB P07437 1/20 0.42
TUBA3C P0DPH7 1/20 0.42
TUBA1B P68363 1/20 0.42
TUBA4A P68366 1/20 0.42
TUBB4B P68371 1/20 0.42
TUBB3 Q13509 1/20 0.42
TUBB2A Q13885 1/20 0.42
TUBB8 Q3ZCM7 1/20 0.42
TUBA3E Q6PEY2 1/20 0.42

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
SCHEMBL30308312 1.00 CYP2A6 (0.51) CYP2A6MAPK11MAPK14CHRNA7MCL1
SCHEMBL28936102 0.92 MAPK11 (0.48) CYP2A6MAPK11MAPK14CHRNA7MCL1
SCHEMBL103922 0.85 TUBB4A (0.56) CYP2A6CHRNA7KDM4EHCAR3TUBB4A
SCHEMBL30233739 0.85 TUBB4A (0.56) CYP2A6CHRNA7KDM4EHCAR3TUBB4A
SCHEMBL2610256 0.85 CYP2A6 (0.51) CYP2A6MAPK11MAPK14CHRNA7KDM2B
SCHEMBL4102767 0.84 AR (0.53) CYP2A6MAPK11MAPK14CHRNA7KDM2B
Hydrazine SCHEMBL1997343 0.82 TUBB4A (0.54) CYP2A6CHRNA7KDM4EHCAR3TUBB4A
SCHEMBL30317473 0.81 MAPK11 (0.53) CYP2A6MAPK11MAPK14CHRNA7KDM2B
SCHEMBL30623233 0.81 KDM4E (0.56) CYP2A6MAPK11MAPK14CHRNA7KDM2B
SCHEMBL232145 0.81 KDM4E (0.56) CYP2A6MAPK11MAPK14CHRNA7KDM2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111295382-B Bridged bicyclic compounds as farnesyl ester X receptor modulators 百时美施贵宝公司 2024-02-02 CN claimed
EP-2155739-B1 2-CYCLOPROPYL-THIAZOLE DERIVATIVES ACTELION PHARMACEUTICALS LTD (CH) 2010-10-06 EP claimed
US-20100222328-A1 2-CYCLOPROPYL-THIAZOLE DERIVATIVES ACTELION PHARMACEUTICALS LTD. (CH) 2010-09-02 US claimed
US-20100222396-A1 4-ARYL-BUTANE-1,3-DIAMIDES NOVARTIS AG (CH) 2010-09-02 US claimed
WO-2010086366-A1 4-ARYL-BUTANE-1,3-DIAMIDES NOVARTIS AG (CH) 2010-08-05 WO claimed
CN-122039051-A Composite coating for high-wear-resistance sliding bearing and preparation method thereof 成都工业职业技术学院 2026-05-15 CN disclosed
WO-2025231152-A1 COMPOUNDS AND METHODS FOR RESTORING BETA-ADRENERGIC RECEPTOR FUNCTION THE CLEVELAND CLINIC FOUNDATION (US) 2025-11-06 WO disclosed
US-20250136592-A1 C-LINKED INHIBITORS OF ENL/AF9 YEATS BRIDGE MEDICINES 2025-05-01 US disclosed
CN-116239768-B Indole polyketone and preparation method thereof 南阳师范学院 2024-11-08 CN disclosed
CN-116253673-B Indole sulfonated monomer, indole sulfonated polymer, proton exchange membrane and preparation method thereof 南阳师范学院 2024-10-18 CN disclosed
WO-2024179405-A1 CLASS OF CINNAMAMIDE DERIVATIVES AND APPLICATION THEREOF 上海交通大学 2024-09-06 WO disclosed
CN-118546081-A Cinnamide derivative and application thereof 上海交通大学 2024-08-27 CN disclosed
EP-0915872-A1 SUBSTITUTED BISINDOLYLMALEIMIDES FOR THE INHIBITION OF CELL PROLIFERATION F. HOFFMANN-LA ROCHE AG (CH) 1999-05-19 EP disclosed
WO-1999020623-A1 INDOLE DERIVATIVE USEFUL AS ENDOTHELIN RECEPTOR ANTAGONIST PFIZER LIMITED (GB) 1999-04-29 WO disclosed
US-5856517-A ANTIPROLIFERATIVE AGENTS USEFUL IN THE TREATMENT OF CANCER. HOFFMANN-LA ROCHE INC. (US) 1999-01-05 US disclosed
EP-0539117-B1 Compounds useful as leukotriene antagonists LILLY CO ELI (GB) 1998-03-11 EP disclosed
WO-1998004552-A1 SUBSTITUTED BISINDOLYLMALEIMIDES FOR THE INHIBITION OF CELL PROLIFERATION F. HOFFMANN-LA ROCHE AG (CH) 1998-02-05 WO disclosed
US-5410061-A Leukotriene antagonist LILLY INDUSTRIES LIMITED (GB) 1995-04-25 US disclosed
EP-0539117-A1 Compounds useful as leukotriene antagonists LILLY INDUSTRIES LIMITED (GB) 1993-04-28 EP disclosed
EP-0409027-A1 Indole derivatives, process for their preparation and their use in pharmaceuticals BAYER AG (DE) 1991-01-23 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 (3 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-20100222396-A1 4-ARYL-BUTANE-1,3-DIAMIDES CYP11B2, CYP11B1, BBC3 CYP2A6 127/4885MAPK11 480/4885MAPK14 796/4885
US-20100222328-A1 2-CYCLOPROPYL-THIAZOLE DERIVATIVES HCRTR2, HCRTR1, NPY2R CYP2A6 692/4885MAPK11 3680/4885MAPK14 4093/4885
US-20250136592-A1 C-LINKED INHIBITORS OF ENL/AF9 YEATS MLLT3, MLLT1, YEATS2 CYP2A6 3494/4885MAPK11 839/4885MAPK14 1682/4885

“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.