Acetic Acid

Acetic Acid

SCHEMBL320127

CC(=O)[O-].CC[N+](CC)(CC)CCO

nearest known ligand 0.40

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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 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.40
BBOX1 O75936 2/20 0.35
DNM1 Q05193 4/20 0.33
TSHR P16473 1/20 0.33
NFKB1 P19838 1/20 0.33
KCNA1 Q09470 1/20 0.33
MEN1 O00255 1/20 0.32
LMNA P02545 1/20 0.32
KMT2A Q03164 1/20 0.32
CYP3A4 P08684 1/20 0.32
SLC5A7 Q9GZV3 1/20 0.32
KDM4E B2RXH2 1/20 0.32
PMP22 Q01453 1/20 0.32
ATM Q13315 1/20 0.32
FFAR3 O14843 1/20 0.31
HDAC3 O15379 1/20 0.31
HDAC1 Q13547 1/20 0.31
HDAC2 Q92769 1/20 0.31
HDAC8 Q9BY41 1/20 0.31
ALDH1A1 P00352 1/20 0.30

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
Bicarbonate SCHEMBL8410039 0.92 BBOX1 (0.37) BBOX1DNM1TSHRNFKB1KCNA1
Bicarbonate SCHEMBL8857321 0.90 BBOX1 (0.35) BBOX1DNM1TSHRNFKB1KCNA1
Bicarbonate SCHEMBL8410024 0.90 BBOX1 (0.35) BBOX1DNM1TSHRNFKB1KCNA1
Acetic Acid SCHEMBL28010749 0.87 CA1 (0.47) CA1BBOX1DNM1MEN1LMNA
Methacrylic Acid SCHEMBL2351340 0.87 BBOX1 (0.31) BBOX1
Acetic Acid SCHEMBL320013 0.86 DNM1 (0.41) CA1BBOX1DNM1KDM4EALDH1A1
Bicarbonate SCHEMBL8857423 0.84 TSHR (0.37) DNM1TSHRNFKB1KCNA1MEN1
Fumaric Acid SCHEMBL2353231 0.84 CA1 (0.40) CA1BBOX1DNM1
Fumaric Acid SCHEMBL2355570 0.84 CA1 (0.40) CA1BBOX1DNM1
Fumaric Acid SCHEMBL2353238 0.84 CA1 (0.40) CA1BBOX1DNM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10717880-B2 Polyisocyanate-based anti-corrosion coating HUNTSMAN INTERNATIONAL LLC (US) 2020-07-21 US disclosed
US-10030094-B2 Polyisocyanurate-based syntactic coating for offshore applications HUNTSMAN INTERNATIONAL LLC (US) 2018-07-24 US disclosed
US-9926479-B2 Materials comprising a matrix and process for preparing them HUNTSMAN INTERNATIONAL LLC (US) 2018-03-27 US disclosed
US-9534072-B2 Polyisocyanate-based adhesive HUNTSMAN INTERNATIONAL LLC (US) 2017-01-03 US disclosed
EP-2300509-B1 A POLYISOCYANURATE-BASED SYNTACTIC COATING FOR OFFSHORE APPLICATIONS HUNTSMAN INT LLC (US) 2016-08-10 EP disclosed
EP-2245081-B1 ELASTOMERIC MATERIALS HAVING A HIGH HARDBLOCK CONTENT AND PROCESS FOR PREPARING THEM HUNTSMAN INT LLC (US) 2015-09-16 EP disclosed
US-20150125704-A1 Polyisocyanate-Based Anti-Corrosion Coating HUNTSMAN INTERNATIONAL LLC 2015-05-07 US disclosed
US-8962142-B2 Polyisocyanate-based anti-corrosion coating HUNTSMAN INTERNATIONAL LLC (US) 2015-02-24 US disclosed
CN-102482489-B Materials comprising a matrix and process for preparing them HUNTSMAN INT LLC 2014-02-19 CN disclosed
CN-101945910-B Elastomeric materials having high hardblock content and process for making them HUNTSMAN INT LLC 2013-09-18 CN disclosed
EP-1970420-A1 Polyisocyanate-based adhesive composition HUNTSMAN INTERNATIONAL LLC (US) 2008-09-17 EP disclosed
US-7405258-B2 Method for producing polyurethane emulsion for aqueous one-component coating agent NIPPON POLYURETHANE INDUSTRY CO., LTD. (JP) 2008-07-29 US disclosed
US-20070155894-A1 Method for producing polyurethane emulsion for aqueous one-component coating agent NIPPON POLYURETHANE INDUSTRY CO., LTD. 2007-07-05 US disclosed
CN-1930257-A Process for producing polyurethane emulsion for water-based one-pack type coating material NIPPON POLYURETHANE KOGYO KK (JP) 2007-03-14 CN disclosed
EP-1721947-A1 PROCESS FOR PRODUCING POLYURETHANE EMULSION FOR WATER-BASED ONE-PACK TYPE COATING MATERIAL Nippon Polyurethane Industry Co., Ltd. (JP) 2006-11-15 EP disclosed
CN-1241990-C Polyisocyanate curing agent for laminated material adhesive and its preparation method NIPPON POLYURETHANE KOGYO KK (JP) 2006-02-15 CN disclosed
US-6596819-B2 An isocyanate group-terminated prepolymer having isocyanurate group and urethane group, obtained by reacting an organic polyisocyanate containing at least (a1) an aromatic diisocyanate with an active hydrogen group-containing compound NIPPON POLYURETHANE INDUSTRY CO., LTD. (JP) 2003-07-22 US disclosed
US-20030083451-A1 Polyisocyanate curing agent for laminate adhesive and process for production thereof NIPPON POLYURETHANE INDUSTRY CO., LTD. (JP) 2003-05-01 US disclosed
CN-1396210-A Polyisocyanate curing agent for laminated material adhesive and its preparation method NIPPON POLYURETHANE KOGYO KK (JP) 2003-02-12 CN disclosed
US-4285789-A COATING A CATHODE WITH A POLYETHERURETHANE COPOLYMER HAVING TERTIARY AMINE, QUARTENARY AMMONIUM, AND BLOCKED ISOCYANATE GROUPS MITSUBISHI CHEMICAL INDUSTRIES, LTD. (JP) 1981-08-25 US disclosed