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.
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 SCHEMBL998512 | 1.00 | FFAR3 (0.58) | — | |
| Acetic Acid SCHEMBL7456705 | 1.00 | FFAR3 (0.58) | — | |
| Acetic Acid SCHEMBL23548939 | 1.00 | FFAR3 (0.58) | — | |
| Acetic Acid SCHEMBL9053450 | 0.96 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL3645655 | 0.96 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL2907405 | 0.96 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL3451040 | 0.96 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL9599616 | 0.96 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL2677437 | 0.96 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL7118694 | 0.96 | FFAR3 (0.54) | — |
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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2013058761-A1 | WASTE WATER TREATMENT SYSTEM | COMPASS WATER SOLUTIONS, INC. (US) | 2013-04-25 | — | — | WO | claimed |
| US-6929759-B2 | Composition of matter and its use as a coagulant and flocculent | CU CHEMIE UETIKON AG (CH) | 2005-08-16 | — | — | US | claimed |
| US-20040195184-A1 | Composition of matter and its use as a coagulant and flocculent | CU CHEMIE UETIKON AG | 2004-10-07 | — | — | US | claimed |
| EP-0271180-B2 | Starburst conjugates | DOW CHEMICAL CO (US) | 1997-06-18 | — | — | EP | claimed |
| US-5527524-A | AGRICULTURAL, PHARMACEUTICAL, DRUG DELIVERY | THE DOW CHEMICAL COMPANY (US) | 1996-06-18 | — | — | US | claimed |
| WO-1988001178-A1 | STARBURST CONJUGATES | THE DOW CHEMICAL COMPANY (US) | 1988-02-25 | — | — | WO | claimed |
| US-4167601-A | Method of depositing a stress-free electroless copper deposit | WESTERN ELECTRIC COMPANY, INC. (US) | 1979-09-11 | — | — | US | claimed |
| WO-2013058761-A1 | WASTE WATER TREATMENT SYSTEM | COMPASS WATER SOLUTIONS, INC. (US) | 2013-04-25 | — | — | WO | disclosed |
| US-6929759-B2 | Composition of matter and its use as a coagulant and flocculent | CU CHEMIE UETIKON AG (CH) | 2005-08-16 | — | — | US | disclosed |
| US-20040195184-A1 | Composition of matter and its use as a coagulant and flocculent | CU CHEMIE UETIKON AG | 2004-10-07 | — | — | US | disclosed |
| US-6503898-B1 | Administering 4,7-dibenzyl-5,6-dihydroxy-N,N*-di(m-aminobenzyl)--1,3-diazepin-2-one or salt to treat human immunodeficiency virus infection | BRISTOL-MYERS SQUIBB PHARMA COMPANY | 2003-01-07 | — | — | US | disclosed |
| US-RE37781-E1 | VIRICIDES, PROTEASE INHIBITOR | DUPONT PHARMACEUTICALS COMPANY | 2002-07-02 | — | — | US | disclosed |
| EP-1153921-A2 | Cyclic ureas and analogues useful as retroviral protease inhibitors | Dupont Pharmaceuticals Company (US) | 2001-11-14 | — | — | EP | disclosed |
| US-5610294-A | VIRAL TREATMENT | THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) | 1997-03-11 | — | — | US | disclosed |
| EP-0607334-A1 | CYCLIC UREAS AND ANALOGUES USEFUL AS RETROVIRAL PROTEASE INHIBITIORS. | DU PONT MERCK PHARMA (US) | 1994-07-27 | — | — | EP | disclosed |
| WO-1993007128-A1 | CYCLIC UREAS AND ANALOGUES USEFUL AS RETROVIRAL PROTEASE INHIBITIORS | THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) | 1993-04-15 | — | — | WO | disclosed |
| US-4617244-A | Additive for electrolyte of lead-acid batteries | GREENE ROLAND M | 1986-10-14 | — | — | US | disclosed |
| US-4560704-A | SILANE ANCUORING;ATTACHING LIGAUD TO MATRIX | PURDUE RESEARCH FOUNDATION (US) | 1985-12-24 | — | — | US | disclosed |
| US-4228213-A | CONTACTING A SURFACE WITH A SOURCE OF CUPRIC IONS, REDUCING AGENT, COMPLEXING AGENT | WESTERN ELECTRIC COMPANY, INC. (US) | 1980-10-14 | — | — | US | disclosed |
| US-4167601-A | Method of depositing a stress-free electroless copper deposit | WESTERN ELECTRIC COMPANY, INC. (US) | 1979-09-11 | — | — | US | disclosed |