Acetic Acid

Acetic Acid

SCHEMBL4359525

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nearest known ligand 0.53

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
ESR1 known ✓ P03372 1/20 0.39
LMNA P02545 4/20 0.53
SLC15A2 Q16348 1/20 0.53
CAMK2A Q9UQM7 1/20 0.53
EGLN1 Q9GZT9 2/20 0.50
ALKBH5 Q6P6C2 1/20 0.50
SUCNR1 Q9BXA5 1/20 0.50
GPR84 Q9NQS5 4/20 0.48
FFAR1 O14842 2/20 0.48
FFAR4 Q5NUL3 2/20 0.48
FFAR3 O14843 2/20 0.47
HDAC3 O15379 1/20 0.47
HDAC1 Q13547 1/20 0.47
HDAC2 Q92769 1/20 0.47
HDAC8 Q9BY41 1/20 0.47
LCK P06239 1/20 0.47
FYN P06241 1/20 0.47
SLC22A6 Q4U2R8 2/20 0.44
KDM4E B2RXH2 1/20 0.43
KDM6B O15054 1/20 0.43

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 SCHEMBL7924905 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL2124440 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL8806720 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL5379043 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL8526392 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL9008818 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL5379107 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL4069322 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL5395207 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5
Acetic Acid SCHEMBL1685004 1.00 LMNA (0.53) LMNASLC15A2CAMK2AEGLN1ALKBH5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3695838-A1 TETRAHYDROPYRIDOETHERS FOR TREATMENT OF AGE-RELATED MACULAR DEGENERATION (AMD) Katairo GmbH (DE) 2020-08-19 EP disclosed
US-20160279111-A1 TETRAHYDROPYRIDOETHERS FOR THE TREATMENT OF AMD TAKEDA GMBH (DE) 2016-09-29 US disclosed
US-20160235724-A1 TETRAHYDROPYRIDOETHERS FOR THE TREATMENT OF STARGARDT'S DISEASE KATAIRO GMBH (DE) 2016-08-18 US disclosed
US-9314453-B2 Tetrahydropyridoethers for treatment of AMD KATAIRO GMBH (DE) 2016-04-19 US disclosed
EP-2742939-A1 Tetrahydropyridoethers for treatment of age-related macular degeneration (AMD) Katairo GmbH (DE) 2014-06-18 EP disclosed
EP-2249829-B1 Tetrahydropyridoethers for treatment of age-related macular degeneration (AMD) KATAIRO GMBH (DE) 2014-03-12 EP disclosed
US-20130131101-A1 TETRAHYDROPYRIDOETHERS FOR TREATMENT OF AMD KATAIRO GMBH (DE) 2013-05-23 US disclosed
US-20090182140-A1 Alicyclic Heterocyclic Compound MITSUBISHI TANABE PHARMA CORPORATION (JP) 2009-07-16 US disclosed
EP-1970373-A1 ALICYCLIC HETEROCYCLIC COMPOUND Mitsubishi Tanabe Pharma Corporation (JP) 2008-09-17 EP disclosed
US-7105676-B2 Tetrahydropyridoethers ALTANA PHARMA AG (DE) 2006-09-12 US disclosed
US-20040162310-A1 Tetrahydropyridoethers ALTANA PHARMA AG. 2004-08-19 US disclosed
US-5965527-A CYCLOSPORIN A SULFIDED AT THE 3 POSITION BY R-(CH)N-S-BY REACTING A LITHIUM-ACTIVATED DERIVATIVE WITH THE DISULFIDE; SYNERGISTIC MIXTURE WITH A RETROVIRUS VIRICIDE; SIDE-EFFECT REDUCTION; AIDS AND ARC (AIDS RELATED COMPLEX) RHONE-POULENC RORER, S.A. (FR) 1999-10-12 US 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 (5 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-20090182140-A1 Alicyclic Heterocyclic Compound CCR4, CCR1, HRH4 ESR1 879/4885LMNA 4047/4885SLC15A2 2517/4885
US-20040162310-A1 Tetrahydropyridoethers CYP7A1, CYP2E1, TPMT ESR1 571/4885LMNA 3736/4885SLC15A2 2650/4885
US-20130131101-A1 TETRAHYDROPYRIDOETHERS FOR TREATMENT OF AMD PTGDR, TBXA2R, NR2E3 ESR1 239/4885LMNA 4575/4885SLC15A2 2346/4885
US-20160235724-A1 TETRAHYDROPYRIDOETHERS FOR THE TREATMENT OF STARGARDT'S DISEASE STARD3, MPST, TPMT ESR1 1960/4885LMNA 2703/4885SLC15A2 1967/4885
US-20160279111-A1 TETRAHYDROPYRIDOETHERS FOR THE TREATMENT OF AMD NR2E3, PTGDR, TBXA2R ESR1 251/4885LMNA 4558/4885SLC15A2 2270/4885

“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.