Acetic Acid

Acetic Acid

SCHEMBL1115925

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

nearest known ligand 0.76

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Acetic Acid. 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
▸ ESR1 known ✓ P03372 1/20 0.74
▸ ADRB2 known ✓ P07550 1/20 0.74
▸ ADRA2A known ✓ P08913 1/20 0.74
▸ ADRA2B known ✓ P18089 1/20 0.74
▸ ADRA2C known ✓ P18825 1/20 0.74
▸ CYSLTR1 Q9Y271 3/20 0.74
▸ CYP2C8 P10632 2/20 0.74
▸ CYSLTR2 Q9NS75 2/20 0.74
▸ MEN1 O00255 1/20 0.74
▸ RECQL P46063 1/20 0.74
▸ BLM P54132 1/20 0.74
▸ KMT2A Q03164 1/20 0.74
▸ ABCB11 O95342 1/20 0.74
▸ EGFR P00533 1/20 0.74
▸ NR3C1 P04150 1/20 0.74
▸ FYN P06241 1/20 0.74
▸ PGR P06401 1/20 0.74
▸ ADRB1 P08588 1/20 0.74
▸ ADORA3 P0DMS8 1/20 0.74
▸ CHRM1 P11229 1/20 0.74

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
Acetic Acid SCHEMBL1204496 1.00 CYSLTR1 (0.74) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL1204492 1.00 CYSLTR1 (0.74) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL4540935 1.00 CYSLTR1 (0.74) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL4540939 1.00 CYSLTR1 (0.74) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL1768658 1.00 CYSLTR1 (0.74) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL1592789 0.99 CYSLTR1 (0.73) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL6111295 0.99 CYSLTR1 (0.73) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL1592793 0.99 CYSLTR1 (0.73) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL6111115 0.99 CYSLTR1 (0.73) CYSLTR1CYP2C8CYSLTR2MEN1RECQL
Acetic Acid SCHEMBL1133382 0.99 CYSLTR1 (0.73) 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 75 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2004608-B1 AN IMPROVED PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM GLADE ORGANICS PRIVATE LTD (IN) 2011-09-14 — — EP claimed
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
EP-1709001-A2 SOLID FORMS OF MONTELUKAST ACID Pliva Istrazivanje i Razvoj d.o.o. (HR) 2006-10-11 — — EP claimed
WO-2005073194-A2 SOLID FORMS OF MONTELUKAST ACID PLIVA- ISTRAZIVANJE I RAZVOJ D.O.O. (HR) 2005-08-11 — — WO claimed
EP-3222279-B1 ORAL PHARMACEUTICAL FORMULATION OF MONTELUKAST AND LEVOCETIRIZINE AND METHOD FOR ITS PRODUCTION INVEST BIELANY SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA (PL) 2021-11-17 — — EP disclosed
EP-3397284-A1 BILAYER TABLET FORMULATIONS OF MONTELUKAST AND RUPATADINE Sanovel Ilac Sanayi ve Ticaret A.S. (TR) 2018-11-07 — — EP disclosed
EP-3397285-A1 TABLET FORMULATIONS OF MONTELUKAST SODIUM AND RUPATADINE FUMARATE Sanovel Ilac Sanayi ve Ticaret A.S. (TR) 2018-11-07 — — EP disclosed
WO-2017182644-A1 TABLET FORMULATIONS OF MONTELUKAST SODIUM AND RUPATADINE FUMARATE SANOVEL ILAC SANAYI VE TICARET A.S. (TR) 2017-10-26 — — WO disclosed
WO-2017182641-A1 BILAYER TABLET FORMULATIONS OF MONTELUKAST AND RUPATADINE SANOVEL ILAC SANAYI VE TICARET A.S. (TR) 2017-10-26 — — WO disclosed
EP-3222279-A1 ORAL PHARMACEUTICAL FORMULATION OF MONTELUKAST AND LEVOCETIRIZINE AND METHOD FOR ITS PRODUCTION Invest Bielany Spolky z Ograniczona Odpowiedzialnoscia (PL) 2017-09-27 — — EP disclosed
EP-2949321-A1 MULTILAYER FORMULATIONS OF FEXOFENADINE AND MONTELUKAST Sanovel Ilac Sanayi ve Ticaret A.S. (TR) 2015-12-02 — — EP disclosed
WO-2005105749-A2 PROCESS FOR MAKING MONTELUKAST AND INTERMEDIATES THEREFOR SYNTHON B.V. (NL) 2005-11-10 — — WO disclosed
US-20050245569-A1 Process for making montelukast and intermediates therefor SYNTHON IP INC. 2005-11-03 — — US disclosed
US-20050245568-A1 Process for making montelukast and intermediates therefor SYNTHON BV (NL) 2005-11-03 — — US disclosed
US-20050234241-A1 Process for the preparation of [R-(E)-1-[[[1-[3-[2-[7-chloro-2-quinolinyl]ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]cyclopropaneacetic acid (montelukast) and its pharmaceutically acceptable salts U.S. BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT 2005-10-20 — — US disclosed
US-20050187251-A1 Substituted N-heterocycle derivatives and methods of their use WYETH (US) 2005-08-25 — — US disclosed
US-20050107612-A1 Process for preparation of montelukast and its salts DR. REDDY'S LABORATORIES LIMITED 2005-05-19 — — US disclosed
US-20050107426-A1 Solid-state montelukast SYNTHON BV (NL) 2005-05-19 — — 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 (9 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-20050245568-A1 Process for making montelukast and intermediates therefor CYP51A1, GPR17, CYP27A1 ESR1 4615/4885ADRB2 1251/4885ADRA2A 2472/4885
US-20050107612-A1 Process for preparation of montelukast and its salts MPST, CMA1, TPMT ESR1 4253/4885ADRB2 1009/4885ADRA2A 1926/4885
US-20090182148-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM AP1S1, CMA1, MED1 ESR1 4830/4885ADRB2 333/4885ADRA2A 663/4885
US-20050107426-A1 Solid-state montelukast CYSLTR1, CYSLTR2, LTA4H ESR1 3537/4885ADRB2 674/4885ADRA2A 1414/4885
US-20050245569-A1 Process for making montelukast and intermediates therefor LTA4H, CYP4A11, LTC4S ESR1 4460/4885ADRB2 1280/4885ADRA2A 2481/4885
US-20050234241-A1 Process for the preparation of [R-(E)-1-[[[1-[3-[2-[7-chloro-2-quinolinyl]ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]cyclopropaneacetic acid (montelukast) and its pharmaceutically acceptable salts CMA1, HRH2, HRH1 ESR1 3539/4885ADRB2 40/4885ADRA2A 57/4885
US-20090281323-A1 PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM CMA1, MED1, MPST ESR1 4562/4885ADRB2 549/4885ADRA2A 629/4885
US-20050187251-A1 Substituted N-heterocycle derivatives and methods of their use MAOA, MAOB, SDHA ESR1 547/4885ADRB2 392/4885ADRA2A 253/4885
US-20110105757-A1 METHOD FOR PREPARATION OF MONTELUKAST ACID IN IONIC LIQUID MEDIUM CYSLTR1, LTC4S, CYSLTR2 ESR1 4749/4885ADRB2 1827/4885ADRA2A 2264/4885

“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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