Acetic Acid

Acetic Acid

SCHEMBL22129233

CC(=O)O.COCc1c(F)c(F)c(CO)c(F)c1F

nearest known ligand 0.36

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 13)

geneUniProtsupporting neighboursconfidence
PRKCE Q02156 1/20 0.36
GCGR P47871 1/20 0.35
IMPDH2 P12268 4/20 0.33
ALDH1A1 P00352 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
IGF1R P08069 1/20 0.30
SRC P12931 1/20 0.30
AXL P30530 1/20 0.30
PTK2 Q05397 1/20 0.30
AURKB Q96GD4 1/20 0.30
ALK Q9UM73 1/20 0.30
HCAR2 Q8TDS4 1/20 0.30
RECQL P46063 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
SCHEMBL359266 0.89 GCGR (0.39) GCGRIGF1RSRCAXLPTK2
Propionic Acid SCHEMBL22160486 0.89 FFAR3 (0.37) GCGRIMPDH2
Acetic Acid SCHEMBL28282631 0.85 FFAR3 (0.39) IMPDH2
SCHEMBL22160484 0.78 CA2 (0.42) ALDH1A1TDP1
SCHEMBL22129223 0.78 MMP1 (0.36) PRKCEIMPDH2ALDH1A1TDP1IGF1R
SCHEMBL9766130 0.78 RECQL (0.38) IMPDH2TDP1IGF1RSRCAXL
Alcohol SCHEMBL22129229 0.77 CA2 (0.39) GCGRALDH1A1TDP1
SCHEMBL19478317 0.76 CA2 (0.39) GCGR
SCHEMBL9785635 0.76 CA2 (0.39) GCGR
SCHEMBL19478240 0.76 GCGR (0.35) GCGRIMPDH2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10745334-B2 Method for synthesizing 2,3,5,6-tetrafluoro-4-methoxymethyl benzyl alcohol ZHEJIANG ZHONGXIN FLUORIDE MAT CO LTD (CN) 2020-08-18 US disclosed
US-20200207693-A1 METHOD FOR SYNTHESIZING 2,3,5,6-TETRAFLUORO-4-METHOXYMETHYL BENZYL ALCOHOL ZHEJIANG ZHONGXIN FLUORIDE MAT CO LTD (CN) 2020-07-02 US disclosed
WO-2020124727-A1 SYNTHESIS METHOD FOR 2,3,5,6-TETRAFLUORO-4-METHOXYMETHYL BENZYL ALCOHOL 浙江中欣氟材股份有限公司 2020-06-25 WO disclosed
CN-109438234-B Synthetic method of 2,3,5, 6-tetrafluoro-4-methoxymethyl benzyl alcohol 浙江中欣氟材股份有限公司 2020-04-21 CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10745334-B2 Method for synthesizing 2,3,5,6-tetrafluoro-4-methoxymethyl benzyl alcohol TET2, TH, ALKBH2 PRKCE 2413/4885GCGR 4661/4885IMPDH2 1256/4885
US-20200207693-A1 METHOD FOR SYNTHESIZING 2,3,5,6-TETRAFLUORO-4-METHOXYMETHYL BENZYL ALCOHOL TH, ALKBH2, ALKBH3 PRKCE 2302/4885GCGR 4714/4885IMPDH2 1027/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.