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)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA2 | P00918 | 1/20 | 0.41 |
| ▸ | CA4 | P22748 | 1/20 | 0.41 |
| ▸ | CES2 | O00748 | 1/20 | 0.39 |
| ▸ | CES1 | P23141 | 1/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.39 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.39 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.39 |
| ▸ | TSHR | P16473 | 1/20 | 0.39 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.39 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.38 |
| ▸ | ALPL | P05186 | 1/20 | 0.38 |
| ▸ | POLB | P06746 | 1/20 | 0.38 |
| ▸ | ALPG | P10696 | 1/20 | 0.38 |
| ▸ | GAA | P10253 | 1/20 | 0.38 |
| ▸ | CA1 | P00915 | 1/20 | 0.38 |
| ▸ | NAPRT | Q6XQN6 | 1/20 | 0.38 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.38 |
| ▸ | APEX1 | P27695 | 1/20 | 0.38 |
| ▸ | PTGS2 | P35354 | 1/20 | 0.38 |
| ▸ | LMNA | P02545 | 1/20 | 0.38 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Acetic Acid SCHEMBL9603211 | 1.00 | CA2 (0.41) | CA2CA4CES2CES1ALDH1A1 | |
| Acetic Acid SCHEMBL9603209 | 0.98 | CA2 (0.39) | CA2CA4CES2CES1ALDH1A1 | |
| Bicarbonate SCHEMBL8437546 | 0.93 | CA2 (0.42) | CA2CA4CES2CES1ALDH1A1 | |
| Bicarbonate SCHEMBL11217064 | 0.93 | CA2 (0.42) | CA2CA4CES2CES1ALDH1A1 | |
| Acetic Acid SCHEMBL10794233 | 0.90 | FNTA (0.41) | CA2CA4CES2CA1HSD17B10 | |
| Acetic Acid SCHEMBL7865550 | 0.86 | CA2 (0.41) | CA2CA4CES2CES1ALDH1A1 | |
| Acetic Acid SCHEMBL7871097 | 0.86 | CA2 (0.41) | CA2CA4CES2CES1ALDH1A1 | |
| SCHEMBL7579915 | 0.85 | KMT2A (0.44) | TSHRGAAHSD17B10MAPT | |
| Succinic Acid SCHEMBL6061689 | 0.85 | HDAC3 (0.46) | CA2CA4CES2CES1ALDH1A1 | |
| Benzoic Acid SCHEMBL7874749 | 0.85 | CA2 (0.64) | CA2CA4CES2CES1ALDH1A1 |
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 36 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20160141725-A1 | Electrolytes and Metal Hydride Batteries | BASF CORPORATION | 2016-05-19 | — | — | US | claimed |
| US-6316575-B1 | MELT TRANSESTERIFICATION OF DIOL COMPOUND AND CARBOANTE COMPOUND USING CATALYST COMPRISING A PHOSPHORUS-CONTAINING BASIC COMPOUND QUATERNARY PHOSPHONIUM SALT TO FORM POLYCARBONATE | IDEMITSU KOSAN CO., LTD. (JP) | 2001-11-13 | — | — | US | claimed |
| EP-4255899-A1 | PROCESS FOR THE PREPARATION OF ERIBULIN | Finetech Pharmaceutical Ltd. (IL) | 2023-10-11 | — | — | EP | disclosed |
| CN-115611774-A | Fenpropathrin hapten, artificial antigen and fenpropathrin detection method | 华南农业大学 | 2023-01-17 | — | — | CN | disclosed |
| CN-107710462-B | Electrochemical hydrogen storage electrode and battery | 巴斯夫公司 | 2022-08-02 | — | — | CN | disclosed |
| WO-2022118321-A1 | PROCESS FOR THE PREPARATION OF ERIBULIN | FINETECH PHARMACEUTICAL LTD. (IL) | 2022-06-09 | — | — | WO | disclosed |
| EP-3292578-B1 | ELECTROCHEMICAL HYDROGEN STORAGE ELECTRODES AND CELLS | BASF CORP (US) | 2021-02-24 | — | — | EP | disclosed |
| US-10243240-B2 | Electrolytes and metal hydride batteries | BASF CORPORATION (US) | 2019-03-26 | — | — | US | disclosed |
| EP-3292578-A1 | ELECTROCHEMICAL HYDROGEN STORAGE ELECTRODES AND CELLS | BASF Corporation (US) | 2018-03-14 | — | — | EP | disclosed |
| EP-3218955-A1 | ELECTROLYTES AND METAL HYDRIDE BATTERIES | BASF Corporation (US) | 2017-09-20 | — | — | EP | disclosed |
| US-20160329560-A1 | Electrochemical Hydrogen Storage Electrodes and Cells | BASF CORPORATION (US) | 2016-11-10 | — | — | US | disclosed |
| EP-0623157-B1 | IGNITION RESISTANT CARBONATE POLYMER BLENDS CONTAINING LOW MOLECULAR WEIGHT HALOGENATED EPOXY COMPOUNDS | DOW CHEMICAL CO (US) | 1996-04-17 | — | — | EP | disclosed |
| EP-0623157-A1 | IGNITION RESISTANT CARBONATE POLYMER BLENDS CONTAINING LOW MOLECULAR WEIGHT HALOGENATED EPOXY COMPOUNDS. | DOW CHEMICAL CO (US) | 1994-11-09 | — | — | EP | disclosed |
| US-5350802-A | Ignition resistant carbonate polymer blends containing low molecular weight halogenated epoxy compounds | THE DOW CHEMICAL COMPANY (US) | 1994-09-27 | — | — | US | disclosed |
| WO-1994014866-A1 | SOLVENT FREE EPOXY RESIN COMPOSITIONS | ALLIEDSIGNAL, INC. (US) | 1994-07-07 | — | — | WO | disclosed |
| WO-1993015149-A1 | IGNITION RESISTANT CARBONATE POLYMER BLENDS CONTAINING LOW MOLECULAR WEIGHT HALOGENATED EPOXY COMPOUNDS | THE DOW CHEMICAL COMPANY (US) | 1993-08-05 | — | — | WO | disclosed |
| EP-0291074-B1 | PROCESS FOR PRODUCING QUATERNARY SALTS | MITSUBISHI PETROCHEMICAL CO., LTD. (JP) | 1992-01-29 | — | — | EP | disclosed |
| US-4892944-A | Process for producing quaternary salts | MITSUBISHI PETROCHEMICAL CO., LTD. (JP) | 1990-01-09 | — | — | US | disclosed |
| US-4540810-A | SYNTHESIS GAS, RUTHENIUM CATALYST, ARYLPHOSPHONIUM COCATALYST | TEXACO DEVELOPMENT CORPORATION (US) | 1985-09-10 | — | — | US | disclosed |
| US-4500473-A | CATALYTIC REACTING ALKYL(OR PHENYL) IODIDE OR SULFONATE WITH CARBOXYLATE AND CARBON MONOXIDE IN APROTIC SOLVENT | RHONE-POULENC CHIMIE DE BASE (FR) | 1985-02-19 | — | — | US | disclosed |