Acetic Acid

Acetic Acid

SCHEMBL7902877

CC(=O)O.CC(=O)O.CC(=O)O.CC(=O)O.c1cnc2c(c1)ccc1ncccc12

nearest known ligand 0.77

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
▸ LMNA P02545 5/20 0.77
▸ CYP3A4 P08684 2/20 0.53
▸ ALDH1A1 P00352 5/20 0.49
▸ KDM4E B2RXH2 4/20 0.48
▸ MAPT P10636 3/20 0.48
▸ HTT P42858 3/20 0.48
▸ TDP1 Q9NUW8 3/20 0.48
▸ CCR1 P32246 2/20 0.48
▸ CCR5 P51681 2/20 0.48
▸ CCR8 P51685 2/20 0.48
▸ ALOX15 P16050 2/20 0.48
▸ SMN1; SMN2 Q16637 2/20 0.48
▸ GMNN O75496 1/20 0.48
▸ TP53 P04637 1/20 0.48
▸ HSP90AA1 P07900 1/20 0.48
▸ MMP2 P08253 1/20 0.48
▸ CYP2D6 P10635 1/20 0.48
▸ MMP9 P14780 1/20 0.48
▸ TSHR P16473 1/20 0.48
▸ NFKB1 P19838 1/20 0.48

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 SCHEMBL9177085 1.00 LMNA (0.77) LMNACYP3A4ALDH1A1KDM4EMAPT
Acetic Acid SCHEMBL7908727 0.98 LMNA (0.74) LMNACYP3A4ALDH1A1KDM4EMAPT
Phosphoric Acid SCHEMBL28535198 0.94 LMNA (0.68) LMNACYP3A4ALDH1A1KDM4EMAPT
Acetic Acid SCHEMBL2108732 0.90 LMNA (0.72) LMNACYP3A4ALDH1A1KDM4EMAPT
Acetic Acid SCHEMBL28018617 0.90 LMNA (0.72) LMNACYP3A4ALDH1A1KDM4EMAPT
SCHEMBL28527433 0.90 LMNA (0.89) LMNACYP3A4ALDH1A1KDM4EMAPT
Methyl Alcohol SCHEMBL27642901 0.90 LMNA (0.89) LMNACYP3A4ALDH1A1KDM4EMAPT
Benzene SCHEMBL27538628 0.89 LMNA (0.96) LMNACYP3A4ALDH1A1KDM4EMAPT
Methyl Alcohol SCHEMBL27878296 0.88 LMNA (0.85) LMNACYP3A4ALDH1A1KDM4EMAPT
SCHEMBL28926538 0.88 LMNA (0.68) LMNACYP3A4ALDH1A1KDM4EMAPT

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-6242268-B1 USING WATER-SOLUBLE, FLUORESCENT, RARE EARTH METAL CHELATES AS TAGS ON SPECIFIC BINDING PARTNERS AND DETECTING FLUORESCENT EMISSION FROM SAMPLE AFTER FLUORESCENCE OF AMBIENT SUSBTANCES HAVE DECAYED EG&G WALLAC (FI) 2001-06-05 — — US disclosed
US-5830769-A QUANTITATIVE ANALYSIS; MEASURING FLUORESCENT EMISSION PERKINELMER LIFE SCIENCES, INC. 1998-11-03 — — US disclosed
EP-0272320-B1 HOMOGENEOUS FLUOROASSAY METHODS EMPLOYING FLUORESCENT BACKGROUND REJECTION BAXTER DIAGNOSTICS INC (US) 1994-03-23 — — EP disclosed
US-4925804-A REPORTER MECHANISM FOR BIOSPECIFIC REACTIONS BAXTER INTERNATIONAL INC. (US) 1990-05-15 — — US disclosed
EP-0272320-A4 HOMOGENEOUS FLUOROASSAY METHODS EMPLOYING FLUORESCENT BACKGROUND REJECTION. BAXTER TRAVENOL LAB (US) 1989-08-09 — — EP disclosed
EP-0272320-A1 HOMOGENEOUS FLUOROASSAY METHODS EMPLOYING FLUORESCENT BACKGROUND REJECTION. BAXTER TRAVENOL LAB (US) 1988-06-29 — — EP disclosed
WO-1987007955-A1 HOMOGENEOUS FLUOROASSAY METHODS EMPLOYING FLUORESCENT BACKGROUND REJECTION AND WATER-SOLUBLE RARE EARTH METAL CHELATE FLUOROPHORES BAXTER TRAVENOL LABORATORIES, INC. (US) 1987-12-30 — — WO disclosed
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