Acetic Acid

Acetic Acid

SCHEMBL2086595

CC(=O)O.NC1=NC(c2ccc(C(F)(F)F)nc2)(c2cccc(Br)c2)c2ccccc21

nearest known ligand 0.49

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
BACE1 P56817 11/20 0.49
KCNH2 Q12809 7/20 0.49
P2RX7 Q99572 4/20 0.34
HDAC4 P56524 1/20 0.34
HDAC11 Q96DB2 1/20 0.33
MAP4K4 O95819 1/20 0.32
PIK3CA P42336 1/20 0.32
MINK1 Q8N4C8 1/20 0.32
PI4KB Q9UBF8 1/20 0.32
CTSD P07339 2/20 0.32
NPSR1 Q6W5P4 1/20 0.31
APP P05067 2/20 0.31
MRGPRX4 Q96LA9 1/20 0.31

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
SCHEMBL12785600 0.93 BACE1 (0.55) BACE1KCNH2CTSDNPSR1
Acetic Acid SCHEMBL2084828 0.79 BACE1 (0.47) BACE1KCNH2CTSD
SCHEMBL2086521 0.78 BACE1 (0.50) BACE1KCNH2CTSDNPSR1
SCHEMBL2085979 0.78 BACE1 (0.79) BACE1KCNH2
Trifluoroacetic Acid SCHEMBL2086620 0.77 BACE1 (0.55) BACE1KCNH2CTSDNPSR1
SCHEMBL4002677 0.77 BACE1 (0.46) BACE1KCNH2CTSD
Trifluoroacetic Acid SCHEMBL2085829 0.76 BACE1 (0.41) BACE1KCNH2CTSD
Trifluoroacetic Acid SCHEMBL2085852 0.75 BACE1 (0.38) BACE1KCNH2CTSD
SCHEMBL2084141 0.74 BACE1 (0.46) BACE1KCNH2CTSDNPSR1
SCHEMBL2086591 0.74 BACE1 (0.55) BACE1KCNH2CTSD

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
CN-101506162-B Substituted isoindoles as bace inhibitors and their use ASTRAZENECA AB 2012-06-27 CN disclosed
US-20110059992-A1 New Compounds ASTRAZENECA AB (SE) 2011-03-10 US disclosed
US-7855213-B2 Compounds ASTRAZENECA AB (SE) 2010-12-21 US disclosed
CN-101506162-A Substituted isoindoles as bace inhibitors and their use ASTRAZENECA AB (SE) 2009-08-12 CN disclosed
EP-2035378-A1 SUBSTITUTED ISOINDOLES AS BACE INHIBITORS AND THEIR USE AstraZeneca AB (SE) 2009-03-18 EP disclosed
US-20080171771-A1 New Compounds 391 ASTRAZENECA AB (SE) 2008-07-17 US disclosed
WO-2007149033-A1 SUBSTITUTED ISOINDOLES AS BACE INHIBITORS AND THEIR USE ASTRAZENECA AB (SE) 2007-12-27 WO 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-20110059992-A1 New Compounds MAPT, PSEN2, PSEN1 BACE1 5/4885KCNH2 3126/4885P2RX7 3353/4885
US-20080171771-A1 New Compounds 391 PSEN2, PSEN1, MAPT BACE1 4/4885KCNH2 2710/4885P2RX7 3246/4885

“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.