SCHEMBL1593088

SCHEMBL1593088

CC(=O)OC(C)(C)c1ccccc1CC[C@@H](SCC1CC1)c1cccc(/C=C/c2ccc3ccc(Cl)cc3n2)c1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYSLTR1 Q9Y271 3/20 0.64
▸ CYP2C8 P10632 2/20 0.63
▸ CYSLTR2 Q9NS75 2/20 0.63
▸ MEN1 O00255 1/20 0.63
▸ RECQL P46063 1/20 0.63
▸ BLM P54132 1/20 0.63
▸ KMT2A Q03164 1/20 0.63
▸ ABCB11 O95342 1/20 0.63
▸ EGFR P00533 1/20 0.63
▸ ESR1 P03372 1/20 0.63
▸ NR3C1 P04150 1/20 0.63
▸ FYN P06241 1/20 0.63
▸ PGR P06401 1/20 0.63
▸ ADRB2 P07550 1/20 0.63
▸ ADRB1 P08588 1/20 0.63
▸ ADRA2A P08913 1/20 0.63
▸ ADORA3 P0DMS8 1/20 0.63
▸ CHRM1 P11229 1/20 0.63
▸ ADRB3 P13945 1/20 0.63
▸ ADRA2B P18089 1/20 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
SCHEMBL1768661 1.00 CYSLTR1 (0.64) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL1115929 1.00 CYSLTR1 (0.64) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL4540937 1.00 CYSLTR1 (0.64) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL1204494 1.00 CYSLTR1 (0.64) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL6109991 0.99 CYSLTR1 (0.63) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL1592792 0.99 CYSLTR1 (0.63) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL6111299 0.99 CYSLTR1 (0.63) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL2076669 0.99 CYSLTR1 (0.63) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
SCHEMBL4250432 0.93 CYSLTR1 (0.54) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL1204496 0.90 CYSLTR1 (0.74) CYSLTR1CYP2C8CYSLTR2MEN1RECQL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110105757-A1 METHOD FOR PREPARATION OF MONTELUKAST ACID IN IONIC LIQUID MEDIUM HANMI PHARM. CO., LTD. (KR) 2011-05-05 — — US claimed
US-20090281323-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM GLADE ORGANICS PRIVATE LIMITED (IN) 2009-11-12 — — US claimed
US-20090182148-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM CHAWLA HARMANDER SINGH PAL 2009-07-16 — — US claimed
US-11844861-B2 Topical Montelukast formulations TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2023-12-19 — — US disclosed
US-20220016028-A1 TOPICAL MONTELUKAST FORMULATIONS TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2022-01-20 — — US disclosed
US-11173117-B2 Topical Montelukast formulations TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2021-11-16 — — US disclosed
US-20210236423-A1 TOPICAL MONTELUKAST FORMULATIONS TARO PHARMACEUTICAL INDUSTRIES LTD. (IL) 2021-08-05 — — US disclosed
EP-2004608-B1 AN IMPROVED PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM GLADE ORGANICS PRIVATE LTD (IN) 2011-09-14 — — EP disclosed
US-20110092708-A1 PROCESS FOR THE PREPARATION OF MONTELUKAST AND ITS SALTS THEREOF MYLAN LABORATORIES LIMITED (IN) 2011-04-21 — — US disclosed
US-20090281323-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM GLADE ORGANICS PRIVATE LIMITED (IN) 2009-11-12 — — US disclosed
US-20090281323-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM GLADE ORGANICS PRIVATE LIMITED (IN) 2009-11-12 — — US disclosed
US-20090182148-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM CHAWLA HARMANDER SINGH PAL 2009-07-16 — — US disclosed
US-20090182148-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM CHAWLA HARMANDER SINGH PAL 2009-07-16 — — US disclosed
EP-2004608-A1 AN IMPROVED PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM Glade Organics Private Limited (IN) 2008-12-24 — — EP disclosed
WO-2007116240-A1 AN IMPROVED PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM GLADE ORGANICS PRIVATE LIMITED (IN) 2007-10-18 — — WO 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 (8 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-11844861-B2 Topical Montelukast formulations CYSLTR1, CYSLTR2, SYMPK CYSLTR1 1/4885CYP2C8 2537/4885CYSLTR2 2/4885
US-11173117-B2 Topical Montelukast formulations CYSLTR1, CYSLTR2, SYMPK CYSLTR1 1/4885CYP2C8 2326/4885CYSLTR2 2/4885
US-20090182148-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM AP1S1, CMA1, MED1 CYSLTR1 17/4885CYP2C8 2439/4885CYSLTR2 26/4885
US-20110092708-A1 PROCESS FOR THE PREPARATION OF MONTELUKAST AND ITS SALTS THEREOF CMA1, LTC4S, LTA4H CYSLTR1 4/4885CYP2C8 1889/4885CYSLTR2 5/4885
US-20090281323-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM CMA1, MED1, MPST CYSLTR1 8/4885CYP2C8 1703/4885CYSLTR2 28/4885
US-20110105757-A1 METHOD FOR PREPARATION OF MONTELUKAST ACID IN IONIC LIQUID MEDIUM CYSLTR1, LTC4S, CYSLTR2 CYSLTR1 1/4885CYP2C8 3488/4885CYSLTR2 3/4885
US-20210236423-A1 TOPICAL MONTELUKAST FORMULATIONS CYSLTR1, CYSLTR2, SYMPK CYSLTR1 1/4885CYP2C8 2326/4885CYSLTR2 2/4885
US-20220016028-A1 TOPICAL MONTELUKAST FORMULATIONS CYSLTR1, CYSLTR2, SYMPK CYSLTR1 1/4885CYP2C8 2537/4885CYSLTR2 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.

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