Batefenterol

Batefenterol

SCHEMBL385358

COc1cc(NC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)c(Cl)cc1CNCC(O)c1ccc(O)c2[nH]c(=O)ccc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB2CHRM2CHRM3

The experimentally established mechanism targets of Batefenterol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
ADRB2 known ✓ P07550 20/20 1.00
CHRM3 known ✓ P20309 20/20 1.00
CHRM2 known ✓ P08172 1/20 1.00

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
Batefenterol SCHEMBL384465 1.00 ADRB2 (1.00) ADRB2CHRM3CHRM2
Batefenterol SCHEMBL384466 1.00 ADRB2 (1.00) ADRB2CHRM3CHRM2
Batefenterol SCHEMBL29372665 1.00 ADRB2 (1.00) ADRB2CHRM3CHRM2
Batefenterol SCHEMBL30299015 1.00 ADRB2 (1.00) ADRB2CHRM3CHRM2
Batefenterol SCHEMBL1999609 0.98 ADRB2 (0.97) ADRB2CHRM3CHRM2
Batefenterol SCHEMBL29380164 0.98 ADRB2 (0.97) ADRB2CHRM3CHRM2
Batefenterol SCHEMBL380875 0.96 ADRB2 (0.93) ADRB2CHRM3CHRM2
SCHEMBL19173093 0.94 ADRB2 (0.90) ADRB2CHRM3CHRM2
SCHEMBL741252 0.94 CHRM3 (1.00) ADRB2CHRM3CHRM2
SCHEMBL827897 0.94 ADRB2 (0.88) ADRB2CHRM3CHRM2

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1615889-A2 BIPHENYL DERIVATIVES HAVING BETA2 ADRENERGIC RECEPTOR AGONIST AND MUSCARINIC RECEPTOR ANTAGONIST ACTIVITY Theravance Inc (US) 2006-01-18 EP claimed
WO-2004074246-A2 BIPHENYL DERIVATIVES HAVING BETA2 ADRENERGIC RECEPTOR AGONIST AND MUSCARINIC RECEPTOR ANTAGONIST ACTIVITY THERAVANCE INC. (US) 2004-09-02 WO claimed
EP-3244876-A1 PHARMACEUTICAL COMBINATION GlaxoSmithKline Intellectual Property Development Limited (GB) 2017-11-22 EP disclosed
WO-2016113216-A1 PHARMACEUTICAL COMBINATION GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) 2016-07-21 WO disclosed
US-8754223-B2 Crystalline form of a biphenyl compound THERAVANCE, INC. (US) 2014-06-17 US disclosed
US-20130289281-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND THERAVANCE, INC. (US) 2013-10-31 US disclosed
US-8476299-B2 Crystalline form of a biphenyl compound THERAVANCE, INC. (US) 2013-07-02 US disclosed
EP-1778672-B1 Crystalline form of a biphenyl compound THERAVANCE INC (US) 2012-12-19 EP disclosed
US-20120283289-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND THERAVANCE, INC. (US) 2012-11-08 US disclosed
US-8101766-B2 Crystalline form of a biphenyl compound THERAVANCE, INC. (US) 2012-01-24 US disclosed
US-20090221638-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND THERAVANCE BIOPHARMA R&D IP, LLC 2009-09-03 US disclosed
US-7521558-B2 Crystalline form of a biphenyl compound THERAVANCE, INC. (US) 2009-04-21 US disclosed
EP-1981872-A1 SUCCINIC ACID SALT OF BIPHENYL-2-YLCARBAMIC ACID 1-[2-(2-CHLORO-4-{[ (R)-2-HYDROXY-2- (8-HYDROXY-2-OXO-1, 2-DIHYDROQUINOLIN-5-YL) ETH YLAMINOIMETHYL]} -5-METHOXYPHENYLCARBAMOYL) ETHYL]PIPERIDIN-4-YL ESTER AND ITS USE FOR THE TREATMENT OF PULMONARY DISORDERS GLAXO GROUP LIMITED (GB) 2008-10-22 EP disclosed
WO-2007090859-A1 SUCCINIC ACID SALT OF BIPHENYL-2-YLCARBAMIC ACID 1-[2-(2-CHLORO-4-{ [ (R)-2-HYDROXY-2- (8-HYDROXY-2-OXO-1, 2-DIHYDROQUINOLIN-5-YL) ETH YLAMINOIMETHYL] } -5-METHOXYPHENYLCARBAMOYL) ETHYL] PIPERIDIN-4-YL ESTER AND ITS USE FOR THE TREATMENT OF PULMONARY DISORDERS GLAXO GROUP LIMITED (GB) 2007-08-16 WO disclosed
EP-1778672-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND Theravance, Inc. (US) 2007-05-02 EP disclosed
WO-2006023454-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND THERAVANCE, INC. (US) 2006-03-02 WO disclosed
US-20060035931-A1 Crystalline form of a biphenyl compound THERAVANCE, INC. 2006-02-16 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 (4 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-20060035931-A1 Crystalline form of a biphenyl compound H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, ALK, PKD2 ADRB2 1162/4885CHRM3 1116/4885CHRM2 1039/4885
US-20130289281-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, ALK, PKD2 ADRB2 1162/4885CHRM3 1116/4885CHRM2 1039/4885
US-20090221638-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, ALK, PKD2 ADRB2 1162/4885CHRM3 1116/4885CHRM2 1039/4885
US-20120283289-A1 CRYSTALLINE FORM OF A BIPHENYL COMPOUND H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, ALK, PKD2 ADRB2 1162/4885CHRM3 1116/4885CHRM2 1039/4885

“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.