Acetic Acid

Acetic Acid

SCHEMBL17764809

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Ca+2].[K+].[K+].[K+].[K+].[Mg+2]

nearest known ligand 0.73

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
CA1 P00915 2/20 0.73
CA4 P22748 3/20 0.61
FAHD1 Q6P587 1/20 0.46
LMNA P02545 2/20 0.42
FFAR3 O14843 2/20 0.39
TSHR P16473 1/20 0.39
THPO P40225 1/20 0.39
LCK P06239 1/20 0.39
FYN P06241 1/20 0.39
BLM P54132 2/20 0.38
MEN1 O00255 1/20 0.38
LDHA P00338 1/20 0.38
KMT2A Q03164 1/20 0.38
ALOX15 P16050 1/20 0.36
PMP22 Q01453 1/20 0.36
GAA P10253 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
HDAC3 O15379 1/20 0.32
HDAC1 Q13547 1/20 0.32
HDAC2 Q92769 1/20 0.32

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 SCHEMBL8657186 1.00 CA1 (0.73) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL4606705 0.95 CA1 (0.80) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL3642970 0.95 CA1 (0.80) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL9119140 0.95 CA1 (0.80) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL80426 0.95 CA1 (0.80) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL10816445 0.95 CA1 (0.80) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL8855360 0.91 CA1 (0.73) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL9650988 0.91 CA1 (0.73) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL29424258 0.91 CA1 (0.73) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL10777299 0.91 CA1 (0.73) CA1CA4FAHD1LMNAFFAR3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11377672-B2 Producing resins from organic waste products FULL CYCLE BIOPLASTICS LLC (US) 2022-07-05 US disclosed
US-20200270652-A1 Producing Resins from Organic Waste Products FULL CYCLE BIOPLASTICS EUROPEAN PARTNERS I, LLC 2020-08-27 US disclosed
US-10465214-B2 Producing resins from organic waste products FULL CYCLE BIOPLASTICS LLC (US) 2019-11-05 US disclosed
EP-3221460-A1 PRODUCING POLYHYDROXYALKANOATE COPOLYMERS FROM ORGANIC WASTE PRODUCTS Full Cycle Bioplastics Inc. (US) 2017-09-27 EP disclosed
US-20160145659-A1 PRODUCING RESINS FROM ORGANIC WASTE PRODUCTS FULL CYCLE BIOPLASTICS EUROPEAN PARTNERS I, LLC 2016-05-26 US disclosed
WO-2016081902-A1 PRODUCING POLYHYDROXYALKANOATE COPOLYMERS FROM ORGANIC WASTE PRODUCTS FULL CYCLE BIOPLASTICS INC. (US) 2016-05-26 WO disclosed