Acetic Acid

Acetic Acid

SCHEMBL2248274

CC(=O)O.CCO[SiH](OCC)OCC

nearest known ligand 0.41

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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
FFAR3 O14843 3/20 0.41
LCK P06239 1/20 0.41
FYN P06241 1/20 0.41
ALDH1A1 P00352 5/20 0.41
LMNA P02545 1/20 0.41
HSD17B10 Q99714 1/20 0.41
TDP1 Q9NUW8 1/20 0.35
ALOX15 P16050 1/20 0.33
MGAM O43451 1/20 0.33
GAA P10253 1/20 0.33
SI P14410 1/20 0.33
MGAM2 Q2M2H8 1/20 0.33
TSHR P16473 1/20 0.33
SOAT1 P35610 1/20 0.33
HCAR2 Q8TDS4 1/20 0.32
GLO1 Q04760 1/20 0.31
TRPA1 O75762 1/20 0.31
HDAC3 O15379 1/20 0.30
HDAC1 Q13547 1/20 0.30
HDAC2 Q92769 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
Acetone SCHEMBL28132690 0.91 ALDH1A1 (0.43) FFAR3ALDH1A1LMNAHSD17B10TDP1
Carbamic Acid SCHEMBL20814677 0.86 ALOX15 (0.43) FFAR3ALDH1A1LMNAHSD17B10ALOX15
Methacrylic Acid SCHEMBL1419612 0.85 THRB (0.38) ALDH1A1LMNAHSD17B10TDP1MGAM
SCHEMBL22491271 0.83 ALDH1A1 (0.33) ALDH1A1LMNAHSD17B10HCAR2GLO1
Urea SCHEMBL9068018 0.82 ALOX15 (0.46) ALDH1A1LMNAHSD17B10TDP1ALOX15
Methyl Alcohol SCHEMBL27815477 0.81 ALDH1A1 (0.30) ALDH1A1
SCHEMBL35885 0.80
SCHEMBL28028831 0.80
Acrylic Acid SCHEMBL31139542 0.79 LMNA (0.48) ALDH1A1LMNAHSD17B10ALOX15TSHR
SCHEMBL27995375 0.79 ALDH1A1 (0.30) ALDH1A1LMNAHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8946068-B2 Patterned doping of semiconductor substrates using photosensitive monolayers INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2015-02-03 US disclosed
US-20130330918-A1 PATTERNED DOPING OF SEMICONDUCTOR SUBSTRATES USING PHOTOSENSITIVE MONOLAYERS INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2013-12-12 US disclosed
US-8513642-B2 Patterned doping of semiconductor substrates using photosensitive monolayers INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2013-08-20 US disclosed
US-8354333-B2 Patterned doping of semiconductor substrates using photosensitive monolayers INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2013-01-15 US disclosed
US-20120273925-A1 PATTERNED DOPING OF SEMICONDUCTOR SUBSTRATES USING PHOTOSENSITIVE MONOLAYERS INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2012-11-01 US disclosed
US-20110186969-A1 PATTERNED DOPING OF SEMICONDUCTOR SUBSTRATES USING PHOTOSENSITIVE MONOLAYERS INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2011-08-04 US disclosed
US-4152286-A USES TWO SOLVENTS WITH DIFFERENT BOILING POINTS TEXAS INSTRUMENTS INCORPORATED (US) 1979-05-01 US disclosed