Known targets — ChEMBL curated mechanism
ADRB1CDK4CDK6CHRM2CHRM3DPP4DRD2DRD3DRD4EGFRHRH1HTR1BHTR1DHTR1FHTR2AHTR2CHTR4SLC6A2SLC6A4
The experimentally established mechanism targets of Succinic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| Succinic Acid SCHEMBL9508104 | 1.00 | LMNA (0.60) | — | |
| Succinic Acid SCHEMBL21776708 | 1.00 | LMNA (0.60) | — | |
| Succinic Acid SCHEMBL29461603 | 0.97 | LMNA (0.56) | — | |
| Succinic Acid SCHEMBL27324587 | 0.97 | LMNA (0.56) | — | |
| Succinic Acid SCHEMBL30298887 | 0.94 | LMNA (0.53) | — | |
| Succinic Acid SCHEMBL155053 | 0.93 | LMNA (0.60) | — | |
| Succinic Acid SCHEMBL105373 | 0.93 | — | — | |
| Succinic Acid SCHEMBL18889846 | 0.93 | LMNA (0.60) | — | |
| Succinic Acid SCHEMBL151456 | 0.93 | LMNA (0.60) | — | |
| Succinic Acid SCHEMBL104934 | 0.93 | — | — |
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 434 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20240315956-A1 | METHOD OF PRODUCTION OF THE COMPOSITION OF CYCLOOXYGENASE-2 (COX-2) INHIBITORS | US Nano Food & Drug INC | 2024-09-26 | — | — | US | claimed |
| EP-4366732-A1 | METHOD OF PRODUCTION OF THE COMPOSITION OF CYCLOOXYGENASE-2 (COX-2) INHIBITORS | US Nano Food & Drug Inc (US) | 2024-05-15 | — | — | EP | claimed |
| CN-117813089-A | Process for producing cyclooxygenase-2 (COX-2) inhibitor composition | 美国纳米食品药品公司 | 2024-04-02 | — | — | CN | claimed |
| CN-116887840-A | Steroid quaternary ammonium compound, preparation method, preparation and application thereof | 江苏恩华络康药物研发有限公司 | 2023-10-13 | — | — | CN | claimed |
| CN-110195050-B | Preparation method of high-purity asparaginase | 江苏恒瑞医药股份有限公司 | 2023-03-10 | — | — | CN | claimed |
| WO-2023281449-A1 | METHOD OF PRODUCTION OF THE COMPOSITION OF CYCLOOXYGENASE-2 (COX-2) INHIBITORS | US Nano Food & Drug INC (US) | 2023-01-12 | — | — | WO | claimed |
| CN-110871063-B | Carbon material treatment liquid and preparation method thereof, carbon material and application thereof | 中国石油化工股份有限公司 | 2022-09-27 | — | — | CN | claimed |
| CN-110871064-B | Carbon material combined treatment liquid and preparation method thereof, and carbon material and application thereof | 中国石油化工股份有限公司 | 2022-09-23 | — | — | CN | claimed |
| CN-114160157-B | Method for supplementing potassium acetate auxiliary agent | 北京水木滨华科技有限公司 | 2022-09-16 | — | — | CN | claimed |
| CN-114621948-A | Efficient nucleic acid extraction kit and use method thereof | 江苏默乐生物科技股份有限公司 | 2022-06-14 | — | — | CN | claimed |
| US-20080260948-A1 | INK AND INK JET RECORDING METHOD | CANON KABUSHIKI KAISHA (JP) | 2008-10-23 | — | — | US | claimed |
| EP-1312261-B1 | Aqueous compositions containing a haloalkynyl compound and a buffer for providing biocidal activity and for stabilising end-use formulations | TROY TECHNOLOGY CORP INC (US) | 2006-08-30 | — | — | EP | claimed |
| CN-1777415-A | Medicinal composition containing edible acid or its acid salt and its use | XIAO XINGREN (CN) | 2006-05-24 | — | — | CN | claimed |
| EP-1312261-A1 | Aqueous compositions containing a haloalkynyl compound and a buffer for providing biocidal activity and for stabilising end-use formulations | Troy Technology Corporation, Inc. (US) | 2003-05-21 | — | — | EP | claimed |
| EP-0831706-B1 | NON-AQUEOUS COMPOSITIONS CONTAINING A HALOALKYNYL COMPOUND AND A BUFFER FOR PROVIDING BIOCIDAL ACTIVITY AND FOR STABILIZING END-USE FORMULATIONS | TROY TECHNOLOGY CORP INC (US) | 2003-05-02 | — | — | EP | claimed |
| US-6124350-A | PAINT CONTAINING A BIOCIDAL COMPOSITION COMPRISING A HALOPROPYNYL COMPOUND AND A BUFFER | TROY TECHNOLOGY CORPORATION, INC. (US) | 2000-09-26 | — | — | US | claimed |
| US-6017955-A | A BUFFER STABILIZER FOR ADJUSTING THE PH OF END-USE FORMULATION BETWEEN 3.0 AND 8.0 TO PREVENT DEGRADATION OF PESTICIDE 3-IODO-2-PROPYNYL BUTYL CARBAMATE | TROY TECHNOLOGY CORPORATION, INC. (US) | 2000-01-25 | — | — | US | claimed |
| EP-0831706-A1 | METHOD OF STABILIZING BIOCIDAL COMPOSITIONS OF HALOALKYNYL COMPOUNDS | TROY CHEMICAL CORPORATION (US) | 1998-04-01 | — | — | EP | claimed |
| WO-1996039836-A1 | METHOD OF STABILIZING BIOCIDAL COMPOSITIONS OF HALOALKYNYL COMPOUNDS | TROY CHEMICAL COMPANY (US) | 1996-12-19 | — | — | WO | claimed |
| EP-0023860-B1 | IMPROVED METHOD FOR PREPARING PLASMINOGEN ACTIVATOR, ACTIVATOR THUS OBTAINED AND MEDICINE COMPRISING IT | PIERRE FABRE S.A. (FR) | 1982-12-22 | — | — | EP | claimed |