Known targets — ChEMBL curated mechanism
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
The experimentally established mechanism targets of Phosphoric 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 | |
|---|---|---|---|---|
| Phosphoric Acid SCHEMBL8714192 | 0.94 | SLC34A1 (0.60) | — | |
| Phosphoric Acid SCHEMBL6399485 | 0.94 | SLC34A1 (0.60) | — | |
| Phosphoric Acid SCHEMBL7968394 | 0.94 | SLC34A1 (0.60) | — | |
| Phosphoric Acid SCHEMBL31011150 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL8711577 | 0.94 | SLC34A1 (0.60) | — | |
| Phosphoric Acid SCHEMBL29592605 | 0.94 | SLC34A1 (0.60) | — | |
| Phosphoric Acid SCHEMBL3396683 | 0.94 | SLC34A1 (0.60) | — | |
| Phosphoric Acid SCHEMBL5474538 | 0.94 | SLC34A1 (0.60) | — | |
| Phosphoric Acid SCHEMBL6694678 | 0.88 | — | — | |
| Phosphoric Acid SCHEMBL2236727 | 0.88 | — | — |
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.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-106376560-B | A kind of charged foam type Iodic acid disinfectant and preparation method thereof | 四川恒通动保生物科技有限公司 | 2019-09-06 | — | — | CN | claimed |
| CN-106376560-A | A charged foam type iodic acid disinfectant and a preparing method thereof | 四川恒通动保生物科技有限公司 | 2017-02-08 | — | — | CN | claimed |
| CN-1800365-A | Production process for efficiently improving American ginseng suspending cell yield | HEBEI BIOLOGY INST (CN) | 2006-07-12 | — | — | CN | claimed |
| CN-117700316-A | Method for preparing protocatechuic acid from lignin | 广东省科学院化工研究所 | 2024-03-15 | — | — | CN | disclosed |
| CN-106376560-B | A kind of charged foam type Iodic acid disinfectant and preparation method thereof | 四川恒通动保生物科技有限公司 | 2019-09-06 | — | — | CN | disclosed |
| CN-108569955-A | A method of preparing three methyl ether of glycerine using glycerine and iodomethane | 深圳市前海博扬研究院有限公司 | 2018-09-25 | — | — | CN | disclosed |
| CN-108569955-A | A method of preparing three methyl ether of glycerine using glycerine and iodomethane | 深圳市前海博扬研究院有限公司 | 2018-09-25 | — | — | CN | disclosed |
| CN-106376560-A | A charged foam type iodic acid disinfectant and a preparing method thereof | 四川恒通动保生物科技有限公司 | 2017-02-08 | — | — | CN | disclosed |
| US-7842818-B2 | Process for preparation of tetrasubstituted 5-azaspiro[2.4]- heptane derivatives and optically active intermediates thereof | DAIICHI SANKYO COMPANY, LIMITED (JP) | 2010-11-30 | — | — | US | disclosed |
| US-20090270637-A1 | PROCESS FOR PREPARATION OF TETRASUBSTITUTED 5-AZASPIRO[2.4]- HEPTANE DERIVATIVES AND OPTICALLY ACTIVE INTERMEDIATES THEREOF | DAIICHI SANKYO COMPANY, LIMITED (JP) | 2009-10-29 | — | — | US | disclosed |
| EP-1930321-A1 | PROCESS FOR PREPARATION OF TETRASUBSTITUTED 5-AZASPIRO[2.4]- HEPTANE DERIVATIVES AND OPTICALLY ACTIVE INTERMEDIATES THEREOF | Daiichi Sankyo Company, Limited (JP) | 2008-06-11 | — | — | EP | disclosed |
| CN-1804026-A | Production process for improving suspension cell saponin content of American ginseng | HEBEI INST OF BIOLOGY (CN) | 2006-07-19 | — | — | CN | disclosed |
| CN-1052859-A | The structure of 17-hydroxyl triptolide alcohol and analogue and preparation method | SKIN DISEASE INST CHINESE ACAD (CN) | 1991-07-10 | — | — | CN | disclosed |
| US-4672138-A | INTERMEDIATES FOR BENZO (B) THIOPHENES; HYPOTENSIVE AGENTS, DIURETICS | HOECHST ROUSSEL PHARMACEUTICALS INC. (US) | 1987-06-09 | — | — | US | disclosed |
| US-4537976-A | Benzo[b]thiophenes | HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) | 1985-08-27 | — | — | US | disclosed |
| US-4528399-A | Benzo[b]thiophenes intermediates | HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) | 1985-07-09 | — | — | US | disclosed |
| US-4436748-A | HYPOTENSIVES, DIURETICS | HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) | 1984-03-13 | — | — | US | disclosed |