Acetic Acid

Acetic Acid

SCHEMBL985917

CC#N.CC(=O)[O-].CC(=O)[O-].CC(C)P(C(C)C)C(C)C.CC(C)P(C(C)C)C(C)C.[Pd+2]

nearest known ligand 0.38

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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 1)

geneUniProtsupporting neighboursconfidence
▸ CA1 P00915 2/20 0.38

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 SCHEMBL28744460 0.87 CA1 (0.50) CA1
Acetic Acid SCHEMBL948383 0.87 CA1 (0.50) CA1
Acetic Acid SCHEMBL4653430 0.85 FFAR3 (0.37) —
Acetic Acid SCHEMBL1469783 0.82 — —
Acetic Acid SCHEMBL1714983 0.82 — —
Acetic Acid SCHEMBL28318641 0.82 CA1 (0.57) CA1
Acetic Acid SCHEMBL8206910 0.76 — —
Acetic Acid SCHEMBL17747086 0.76 CA1 (0.57) CA1
Acetic Acid SCHEMBL29046887 0.76 CA1 (0.57) CA1
Acetic Acid SCHEMBL3173468 0.76 — —

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
US-8329838-B2 Norbornene-type polymers, compositions thereof and lithographic processes using such compositions PROMERUS LLC (US) 2012-12-11 — — US claimed
US-7799883-B2 copolymerizing norbornene monomers containing ester groups, sulonamide groups, ethers, alcohols in presence of (Acetonitrile) bis(triisopropylphosphine)palladium(acetate) tetrakis (pentafluorophenyl)borate catalyst and an optional cocatalyst lithium tetrakis(pentafluorophenyl)borate diethyl etherate PROMERUS LLC (US) 2010-09-21 — — US claimed
EP-1853972-A2 NORBORNENE-TYPE POLYMERS, COMPOSITIONS THEREOF AND LITHOGRAPHIC PROCESSES USING SUCH COMPOSITIONS Promerus LLC (US) 2007-11-14 — — EP claimed
US-20060234164-A1 copolymerizing norbornene monomers containing ester groups, sulonamide groups, ethers, alcohols in presence of (Acetonitrile) bis(triisopropylphosphine)palladium(acetate) tetrakis (pentafluorophenyl)borate catalyst and an optional cocatalyst lithium tetrakis(pentafluorophenyl)borate diethyl etherate PROMERUS LLC (US) 2006-10-19 — — US claimed
WO-2006091802-A2 NORBORNENE-TYPE POLYMERS, COMPOSITIONS THEREOF AND LITHOGRAPHIC PROCESSES USING SUCH COMPOSITIONS PROMERUS LLC (US) 2006-08-31 — — WO claimed
WO-2006091523-A2 NORBORNENE-TYPE POLYMERS, COMPOSITIONS THEREOF AND LITHOGRAPHIC PROCESSES USING SUCH COMPOSITIONS PROMERUS LLC (US) 2006-08-31 — — WO claimed
US-8329838-B2 Norbornene-type polymers, compositions thereof and lithographic processes using such compositions PROMERUS LLC (US) 2012-12-11 — — US disclosed
EP-2510036-A2 NORBORNENE-TYPE POLYMERS HAVING QUATERNARY AMMONIUM FUNCTIONALITY Promerus LLC (US) 2012-10-17 — — EP disclosed
WO-2011072304-A2 NORBORNENE-TYPE POLYMERS HAVING QUATERNARY AMMONIUM FUNCTIONALITY PROMERUS LLC (US) 2011-06-16 — — WO disclosed
US-20110009578-A1 Use Of A Combination Chain Transfer And Activating Agent To Control Molecular Weight And Optical Density Of Pd Catalyzed Norbornene Polymers PROMERUS LLC (US) 2011-01-13 — — US disclosed
US-7759439-B2 Use of a combination chain transfer and activating agent to control molecular weight and optical density of Pd catalyzed norbornene polymers PROMERUS LLC (US) 2010-07-20 — — US disclosed
US-7608382-B2 Method of controlling the differential dissolution rate of photoresist compositions, polycyclic olefin polymers and monomers used for making such polymers PROMERUS LLC (US) 2009-10-27 — — US disclosed
EP-2031007-A2 Norbornene-type polymers, compositions thereof and lithographic processes using such compositions Promerus LLC (US) 2009-03-04 — — EP disclosed
EP-1730773-A1 POLYMERS OF POLYCYCLIC OLEFINS HAVING A POLYHEDRAL OLIGOSILSESQUIOXANE PENDANT GROUP AND USES THEREOF Promerus, LLC (US) 2006-12-13 — — EP disclosed
WO-2006091523-A2 NORBORNENE-TYPE POLYMERS, COMPOSITIONS THEREOF AND LITHOGRAPHIC PROCESSES USING SUCH COMPOSITIONS PROMERUS LLC (US) 2006-08-31 — — WO disclosed
EP-1597629-A2 METHOD OF CONTROLLING THE DIFFERENTIAL DISSOLUTION RATE OF PHOTORESIST COMPOSITIONS Promerus, LLC (US) 2005-11-23 — — EP disclosed
WO-2005081306-A1 POLYMERS OF POLYCYCLIC OLEFINS HAVING A POLYHEDRAL OLIGOSILSESQUIOXANE PENDANT GROUP AND USES THEREOF PROMERUS, LLC (US) 2005-09-01 — — WO disclosed
US-20050192409-A1 Polymers of polycyclic olefins having a polyhedral oligosilsesquioxane pendant group and uses thereof PROMERUS, LLC 2005-09-01 — — US disclosed
WO-2004077160-A2 METHOD OF CONTROLLING THE DIFFERENTIAL DISSOLUTION RATE OF PHOTORESIST COMPOSITIONS PROMERUS, LLC (US) 2004-09-10 — — WO disclosed
US-20040166436-A1 Method of controlling the differential dissolution rate of photoresist compositions, polycyclic olefin polymers and monomers used for making such polymers INTERNATIONAL BUSINESS MACHINES CORPORATION 2004-08-26 — — US disclosed
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