Acetic Acid

Acetic Acid

SCHEMBL4576890

CC(=O)O.CC(C)(C)OC(=O)CN

nearest known ligand 0.38

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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
GLRA1 P23415 1/20 0.35
SLC6A9 P48067 1/20 0.35
OR51E2 Q9H255 1/20 0.35
TDP1 Q9NUW8 1/20 0.34
GAA P10253 3/20 0.33
KDM4E B2RXH2 1/20 0.33
DGAT1 O75907 1/20 0.33
MGAM O43451 1/20 0.33
SI P14410 1/20 0.33
MGAM2 Q2M2H8 1/20 0.33
MAOA P21397 1/20 0.33
MAOB P27338 1/20 0.33
FFAR3 O14843 1/20 0.33
LCK P06239 1/20 0.33
FYN P06241 1/20 0.33
CYP2D6 P10635 1/20 0.33
MTNR1A P48039 5/20 0.33
MTNR1B P49286 5/20 0.33
HDAC3 O15379 1/20 0.33
HDAC1 Q13547 1/20 0.33

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 SCHEMBL23783571 0.98 KDM4E (0.37) GLRA1SLC6A9OR51E2TDP1GAA
SCHEMBL6116105 0.93
SCHEMBL44143 0.93
Hydrochloric Acid SCHEMBL336665 0.90 KDM4E (0.38) GLRA1SLC6A9OR51E2TDP1GAA
Ammonia Solution, Strong SCHEMBL20241550 0.90 TDP1 (0.36) GLRA1SLC6A9OR51E2TDP1GAA
SCHEMBL28278850 0.90 TDP1 (0.36) GLRA1SLC6A9OR51E2TDP1GAA
Hydrochloric Acid SCHEMBL14659623 0.88 TDP1 (0.35) GLRA1SLC6A9OR51E2TDP1GAA
Ethylamine SCHEMBL7474222 0.88 TDP1 (0.35) GLRA1SLC6A9OR51E2TDP1KDM4E
SCHEMBL9725893 0.86 TDP1 (0.34) TDP1KDM4EDGAT1MAOAMAOB
SCHEMBL1225343 0.85 TDP1 (0.35) TDP1GAAKDM4EDGAT1MGAM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111432844-B PSMA-targeting amanitine conjugates 海德堡医药研究有限责任公司 2023-10-27 CN disclosed
WO-2023075435-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE 주식회사 베르티스 2023-05-04 WO disclosed
EP-3684416-B1 PSMA-TARGETING AMANITIN CONJUGATES HEIDELBERG PHARMA RES GMBH (DE) 2023-03-15 EP disclosed
US-11583569-B2 PSMA-targeting amanitin conjugates HEIDELBERG PHARMA RESEARCH GMBH (DE) 2023-02-21 US disclosed
US-20220283131-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTES BERTIS CO., LTD. (KR) 2022-09-08 US disclosed
CN-109651224-B Fluorescent protein cross-linking agent and preparation method thereof 苏州昊帆生物股份有限公司 2022-05-10 CN disclosed
WO-2022050529-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE ㈜베르티스 2022-03-10 WO disclosed
US-20200345807-A1 PSMA-TARGETING AMANITIN CONJUGATES HEIDELBERG PHARMA RESEARCH GMBH (DE) 2020-11-05 US disclosed
EP-3684416-A1 PSMA-TARGETING AMANITIN CONJUGATES Heidelberg Pharma Research GmbH (DE) 2020-07-29 EP disclosed
CN-111432844-A Amanitine conjugates targeting PSMA 海德堡医药研究有限责任公司 2020-07-17 CN disclosed
WO-2019057964-A1 PSMA-TARGETING AMANITIN CONJUGATES HEIDELBERG PHARMA RESEARCH GMBH (DE) 2019-03-28 WO disclosed
CN-102391140-B Preparation method of N-(2- indanyl) amino acid alkyl ester HUNAN FANGSHENG PHARMACEUTICAL CO LTD 2014-08-06 CN disclosed
CN-102391140-A Preparation method of N-(2- indanyl) amino acid alkyl ester HUNAN FANGSHENG PHARMACEUTICAL CO LTD 2012-03-28 CN disclosed
US-20080269240-A1 Novel Adenine Compound Dainippon Sumitomo Pharma Co., Ltd. a corporation of Japan (JP) 2008-10-30 US disclosed
EP-1939199-A1 NOVEL ADENINE COMPOUND Dainippon Sumitomo Pharma Co., Ltd. (JP) 2008-07-02 EP disclosed
US-6359113-B1 USING FUSED RING SYSTEM CONTAINING AT LEAST 4 AROMATIC RINGS, AND GROUP CONTAINING AT LEAST ONE CARBON ATOM WHICH IS CAPABLE OF BONDING TO A GROUP TO BE PROTECTED; SYNTHESIS, SEPARATION RHODIA CHIMIE (FR) 2002-03-19 US disclosed
US-5869605-A Protected compound comprising a protective group removably attached to a compound to be protected RHONE-POULENCCHIMIE (FR) 1999-02-09 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 (3 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-20080269240-A1 Novel Adenine Compound ADORA1, ADORA2A, ADORA3 GLRA1 1438/4885SLC6A9 912/4885OR51E2 3637/4885
US-20200345807-A1 PSMA-TARGETING AMANITIN CONJUGATES FOLH1, ANPEP, PSMA6 GLRA1 2839/4885SLC6A9 4000/4885OR51E2 1552/4885
US-11583569-B2 PSMA-targeting amanitin conjugates FOLH1, ANPEP, PSMA6 GLRA1 2839/4885SLC6A9 4000/4885OR51E2 1552/4885

“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.