SCHEMBL356694

SCHEMBL356694

O=Cc1ccc(C(=O)CNCCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1

nearest known ligand 0.63

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
CHRM3 P20309 20/20 0.63

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
SCHEMBL266337 0.91 CHRM3 (0.60) CHRM3
SCHEMBL355991 0.90 CHRM3 (0.67) CHRM3
SCHEMBL645741 0.89 CHRM3 (0.67) CHRM3
SCHEMBL644299 0.89 CHRM3 (0.64) CHRM3
SCHEMBL645124 0.87 CHRM3 (0.60) CHRM3
SCHEMBL713681 0.87 CHRM3 (0.62) CHRM3
SCHEMBL942924 0.86 CHRM2 (0.61) CHRM3
SCHEMBL643380 0.86 CHRM3 (0.59) CHRM3
SCHEMBL644562 0.86 CHRM3 (0.59) CHRM3
SCHEMBL644406 0.86 CHRM3 (0.64) CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250136550-A1 PROCESSES FOR PREPARING REVEFENACIN AND COMPOSITIONS COMPRISING THE SAME THERAVANCE BIOPHARMA R&D IP, LLC 2025-05-01 US disclosed
US-12258316-B2 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE BIOPHARMA R&D IP, LLC (US) 2025-03-25 US disclosed
US-20240327352-A1 NOVEL PROCESS FOR THE PREPARATION OF 1-(2-{4-[(4-CARBAMOYLPIPERIDIN-1-YL)METHYL]- N-METHYLBENZAMIDO}ETHYL)PIPERIDIN-4-YL N-({1,1'-BIPHENYL}-2-YL)CARBAMATE MSN LABORATORIES PRIVATE LTD, R&D CENTER (IN) 2024-10-03 US disclosed
CN-114573500-B Preparation method of raffinancin intermediate 扬州中宝药业股份有限公司 2024-02-20 CN disclosed
CN-117285458-A Amorphous Lei Fen narasin and preparation method thereof 山东京卫制药有限公司 2023-12-26 CN disclosed
CN-117263849-A Crystal form of raffinacine trihydrate and preparation method thereof 山东京卫制药有限公司 2023-12-22 CN disclosed
WO-2023104920-A1 CRYSTALLINE ACETONE SOLVATE OF REVEFENACIN MEDICHEM, S.A. (ES) 2023-06-15 WO disclosed
US-20220388981-A1 CRYSTALLINE FORMS OF A BIPHENYL COMPOUND THERAVANCE BIOPHARMA R&D IP LLC (US) 2022-12-08 US disclosed
US-11390603-B2 Crystalline forms of a biphenyl compound THERAVANCE BIOPHARMA R&D IP, LLC (US) 2022-07-19 US disclosed
CN-114573500-A Preparation method of lefenacin intermediate 扬州中宝药业股份有限公司 2022-06-03 CN disclosed
US-20070112027-A1 Crystalline forms of a biphenyl compound THERAVANCE, INC. 2007-05-17 US disclosed
US-20060281740-A1 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE BIOPHARMA R&D IP, LLC 2006-12-14 US disclosed
EP-1723114-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS Theravance, Inc. (US) 2006-11-22 EP disclosed
WO-2006099032-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS THERAVANCE, INC. (US) 2006-09-21 WO disclosed
WO-2006099165-A1 CRYSTALLINE FORMS OF A BIPHENYL COMPOUND THERAVANCE, INC. (US) 2006-09-21 WO disclosed
US-20060205779-A1 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE, INC. 2006-09-14 US disclosed
US-20060205775-A1 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE, INC. 2006-09-14 US disclosed
WO-2005087738-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS THERAVANCE, INC. (US) 2005-09-22 WO disclosed
US-20050203133-A1 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE, INC. 2005-09-15 US disclosed
US-20050203138-A1 Biphenylylaminocarbonyl-amino- or -oxypiperidine derivatives, e.g., biphenyl-2-ylcarbamic acid 1-[2-((4-[(4-hydroxybenzylamino)methyl]benzoyl)methylamino)ethyl]piperidin-4-yl ester; treating bronchodilation, asthma and chronic obstructive pulmonary disease (COPD) THERAVANCE, INC. 2005-09-15 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 (11 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-20250136550-A1 PROCESSES FOR PREPARING REVEFENACIN AND COMPOSITIONS COMPRISING THE SAME CYP4B1, KDM4B, CYP3A4 CHRM3 1755/4885
US-20060205775-A1 Biphenyl compounds useful as muscarinic receptor antagonists CHRM2, CHRM3, CHRM1 CHRM3 2/4885
US-11390603-B2 Crystalline forms of a biphenyl compound FFAR1, FFAR4, FFAR3 CHRM3 1386/4885
US-20070112027-A1 Crystalline forms of a biphenyl compound FFAR1, FFAR4, FFAR3 CHRM3 1386/4885
US-20220388981-A1 CRYSTALLINE FORMS OF A BIPHENYL COMPOUND FFAR1, FFAR4, FFAR3 CHRM3 1386/4885
US-20050203133-A1 Biphenyl compounds useful as muscarinic receptor antagonists CHRM2, CHRM1, CHRM3 CHRM3 3/4885
US-20060205779-A1 Biphenyl compounds useful as muscarinic receptor antagonists CHRM2, CHRM1, CHRM3 CHRM3 3/4885
US-20050203138-A1 Biphenylylaminocarbonyl-amino- or -oxypiperidine derivatives, e.g., biphenyl-2-ylcarbamic acid 1-[2-((4-[(4-hydroxybenzylamino)methyl]benzoyl)methylamino)ethyl]piperidin-4-yl ester; treating bronchodilation, asthma and chronic obstructive pulmonary disease (COPD) CHRM1, CHRM2, CHRM3 CHRM3 3/4885
US-12258316-B2 Biphenyl compounds useful as muscarinic receptor antagonists CHRM2, CHRM1, CHRM3 CHRM3 3/4885
US-20240327352-A1 NOVEL PROCESS FOR THE PREPARATION OF 1-(2-{4-[(4-CARBAMOYLPIPERIDIN-1-YL)METHYL]- N-METHYLBENZAMIDO}ETHYL)PIPERIDIN-4-YL N-({1,1'-BIPHENYL}-2-YL)CARBAMATE CYP4B1, CYP1B1, KDM4B CHRM3 357/4885
US-20060281740-A1 Biphenyl compounds useful as muscarinic receptor antagonists CHRM2, CHRM3, CHRM5 CHRM3 2/4885

“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.