Montelukast

Montelukast

SCHEMBL625297

CC(C)(O)c1ccccc1CCC(SCC1(CC(=O)O)CC1)c1cccc(/C=C/c2ccc3ccc(Cl)cc3n2)c1.[NaH]

nearest known ligand 0.99

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CYSLTR1

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYSLTR1 known ✓ Q9Y271 15/20 0.99
CYSLTR2 Q9NS75 14/20 0.99
CYP2C8 P10632 2/20 0.99
MEN1 O00255 1/20 0.99
RECQL P46063 1/20 0.99
BLM P54132 1/20 0.99
KMT2A Q03164 1/20 0.99
ABCB11 O95342 1/20 0.99
EGFR P00533 1/20 0.99
ESR1 P03372 1/20 0.99
NR3C1 P04150 1/20 0.99
FYN P06241 1/20 0.99
PGR P06401 1/20 0.99
ADRB2 P07550 1/20 0.99
ADRB1 P08588 1/20 0.99
ADRA2A P08913 1/20 0.99
ADORA3 P0DMS8 1/20 0.99
CHRM1 P11229 1/20 0.99
ADRB3 P13945 1/20 0.99
ADRA2B P18089 1/20 0.99

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
Montelukast SCHEMBL41733 1.00 CYSLTR1 (0.99) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL4752437 1.00 CYSLTR1 (0.99) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL27474743 1.00 CYSLTR1 (0.99) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL125179 1.00 CYSLTR1 (0.99) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL15375392 1.00 CYSLTR1 (0.99) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL4788144 1.00 CYSLTR1 (0.99) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL4487 0.99 CYSLTR1 (1.00) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL4486 0.99 CYSLTR1 (1.00) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL22207045 0.99 CYSLTR1 (1.00) CYSLTR1CYSLTR2CYP2C8MEN1RECQL
Montelukast SCHEMBL21635556 0.99 CYSLTR1 (1.00) CYSLTR1CYSLTR2CYP2C8MEN1RECQL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116492315-A Montelukast sodium microcapsule, preparation method and application thereof 郑州大学第一附属医院 2023-07-28 CN disclosed
CN-109503476-A A kind of synthesis technology of Montelukast Sodium 哈尔滨珍宝制药有限公司 2019-03-22 CN disclosed
EP-1968943-B1 AN IMPROVED PROCESS FOR THE PREPARATION OF MONTELUKAST AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS MSN LAB LTD (IN) 2013-01-23 EP disclosed
US-8178680-B2 Process for the preparation of Montelukast and its pharmaceutically acceptable salts MSN LABORATORIES LIMITED (IN) 2012-05-15 US disclosed
WO-2012020271-A1 PROCESS FOR THE PREPARATION OF MONTELUKAST SODIUM RICHTER GEDEON NYRT. (HU) 2012-02-16 WO disclosed
EP-2231613-B1 MONTELUKAST BENZHYDRYL PIPERAZINE SALTS AND PROCESS FOR PREPARATION THEREOF TORRENT PHARMACEUTICALS LTD (IN) 2011-10-12 EP disclosed
US-20100292251-A1 MONTELUKAST BENZHYDRYL PIPERAZINE SALTS AND PROCESS FOR PREPARATION THEREOF TORRENT PHARMACEUTICALS LIMITED (IN) 2010-11-18 US disclosed
US-20100069641-A1 PROCESS FOR THE PREPARATION OF SODIUM SALT OF 1-(((1(R)-(3-(2-(7-CHLORO-2-QUINOLINYL)-ETHENYL)PHENYL)-3-(2-(1-HYDROXY-1-METHYLETHYL)PHENYL)PROPYL)SULFANYL)METHYL)CYCLOPROPANEACETIC ACID ZAKLADY FARMACEUTYCZNE POLPHARMA S.A. (PL) 2010-03-18 US disclosed
US-7572930-B2 Process for preparing 1-(mercaptomethyl)cyclopropaneacetic acid, a useful intermediate in the preparation of montelukast and salts thereof CHEMAGIS LTD. (IL) 2009-08-11 US disclosed
US-20090171092-A1 Process for the Preparation of Montelukast and Its Pharmaceutically Acceptable Salts MSN LABORATORIES LIMITED (IN) 2009-07-02 US disclosed
US-20080009629-A1 Novel Form of a Benzenesulfonamide Derivative PLIVA-ISTRAZIVANJE I RAZVOJ D.O.O. (HR) 2008-01-10 US disclosed
US-20070213365-A1 Novel polymorphs of montelukast ammonium salts and processes for preparation therefor CHEMAGIS LTD. (IL) 2007-09-13 US disclosed
US-20070208177-A1 Novel process for preparing 1-(mercaptomethyl)cyclopropaneacetic acid, a useful intermediate in the preparation of montelukast and salts thereof CHEMAGIS LTD. (IL) 2007-09-06 US disclosed
US-20070208178-A1 Reacting the side-chain precursor 1-(mercaptomethyl)cyclopropaneacetic acid (not an ester) with 2-(2-(3S)-(3-(7-chloro-2-quinolinyl)-vinylphenyl)-3-(methanesulfonyloxypropyl)phenyl-2-propanol in a basic solvent mixture; forming an amine salt; and exchanging the amine cation with sodium; 99.5+% pure CHEMAGIS LTD. (IL) 2007-09-06 US disclosed
WO-2007096875-A2 NOVEL POLYMORPHS OF MONTELUKAST AMMONIUM SALTS AND PROCESSES FOR PREPARATION THEREFOR CHEMAGIS LTD. (IL) 2007-08-30 WO disclosed
WO-2007088545-A2 NOVEL PROCESS FOR PREPARING 1-(MERCAPTOMETHYL) CYCLOPROPANEACETIC ACID, A USEFUL INTERMEDIATE IN THE PREPARATION OF MONTELUKAST AND SALTS THEREOF CHEMAGIS LTD. (IL) 2007-08-09 WO disclosed
EP-1429843-B1 COMBINATION OF A PDE INHIBITOR AND A LEUKOTRIENE RECEPTOR ANTAGONIST ALTANA PHARMA AG (DE) 2006-12-27 EP disclosed
US-20060223999-A1 Process for preparing montelukast and precursors thereof CHEMAGIS LTD. (IL) 2006-10-05 US disclosed
US-20050187245-A1 Stable amorphous forms of montelukast sodium CHEMAGIS LTD. (IL) 2005-08-25 US disclosed
US-20050014762-A1 Combination NYCOMED GMBH (DE) 2005-01-20 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 (10 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-20070213365-A1 Novel polymorphs of montelukast ammonium salts and processes for preparation therefor ATP6V1A, ATP6V1H, ATP6V1G1 CYSLTR1 27/4885CYSLTR2 103/4885CYP2C8 614/4885
US-20060223999-A1 Process for preparing montelukast and precursors thereof CMA1, LTC4S, LTB4R2 CYSLTR1 16/4885CYSLTR2 5/4885CYP2C8 718/4885
US-20090171092-A1 Process for the Preparation of Montelukast and Its Pharmaceutically Acceptable Salts CMA1, TPSD1, AP1S1 CYSLTR1 23/4885CYSLTR2 32/4885CYP2C8 676/4885
US-20050187245-A1 Stable amorphous forms of montelukast sodium CMA1, MAST3, LTC4S CYSLTR1 20/4885CYSLTR2 17/4885CYP2C8 3957/4885
US-20100292251-A1 MONTELUKAST BENZHYDRYL PIPERAZINE SALTS AND PROCESS FOR PREPARATION THEREOF CMA1, CYSLTR2, CYSLTR1 CYSLTR1 3/4885CYSLTR2 2/4885CYP2C8 1004/4885
US-20070208178-A1 Reacting the side-chain precursor 1-(mercaptomethyl)cyclopropaneacetic acid (not an ester) with 2-(2-(3S)-(3-(7-chloro-2-quinolinyl)-vinylphenyl)-3-(methanesulfonyloxypropyl)phenyl-2-propanol in a basic solvent mixture; forming an amine salt; and exchanging the amine cation with sodium; 99.5+% pure CYSLTR2, MPST, CMA1 CYSLTR1 4/4885CYSLTR2 1/4885CYP2C8 1092/4885
US-20050014762-A1 Combination PDE4A, PDE4B, PDE3B CYSLTR1 23/4885CYSLTR2 20/4885CYP2C8 1038/4885
US-20070208177-A1 Novel process for preparing 1-(mercaptomethyl)cyclopropaneacetic acid, a useful intermediate in the preparation of montelukast and salts thereof CMA1, CYSLTR1, MPST CYSLTR1 2/4885CYSLTR2 5/4885CYP2C8 1018/4885
US-20100069641-A1 PROCESS FOR THE PREPARATION OF SODIUM SALT OF 1-(((1(R)-(3-(2-(7-CHLORO-2-QUINOLINYL)-ETHENYL)PHENYL)-3-(2-(1-HYDROXY-1-METHYLETHYL)PHENYL)PROPYL)SULFANYL)METHYL)CYCLOPROPANEACETIC ACID SLC7A1, CLIC1, TMT1A CYSLTR1 1267/4885CYSLTR2 1917/4885CYP2C8 2230/4885
US-20080009629-A1 Novel Form of a Benzenesulfonamide Derivative ADH1A, ADH5, ADH1C CYSLTR1 3773/4885CYSLTR2 3571/4885CYP2C8 3787/4885

“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.