Known targets — ChEMBL curated mechanism
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
The experimentally established mechanism targets of Sulfuric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA5A | P35218 | 2/20 | 0.75 |
| ▸ | CA5B | Q9Y2D0 | 2/20 | 0.75 |
| ▸ | TSHR | P16473 | 3/20 | 0.46 |
| ▸ | CA2 | P00918 | 2/20 | 0.46 |
| ▸ | CA1 | P00915 | 1/20 | 0.46 |
| ▸ | NT5E | P21589 | 1/20 | 0.46 |
| ▸ | CA4 | P22748 | 1/20 | 0.46 |
| ▸ | CA6 | P23280 | 1/20 | 0.46 |
| ▸ | CA7 | P43166 | 1/20 | 0.46 |
| ▸ | CA9 | Q16790 | 1/20 | 0.46 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.46 |
| ▸ | BLM | P54132 | 2/20 | 0.43 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.43 |
| ▸ | MEN1 | O00255 | 1/20 | 0.42 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.42 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.42 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.33 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.33 |
| ▸ | NPSR1 | Q6W5P4 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Sulfuric Acid SCHEMBL74093 | 1.00 | — | — | |
| Sulfuric Acid SCHEMBL28664622 | 1.00 | CA5A (0.75) | CA5ACA5BTSHRCA2CA1 | |
| Sulfuric Acid SCHEMBL23294055 | 1.00 | CA5A (0.75) | CA5ACA5BTSHRCA2CA1 | |
| Sulfuric Acid SCHEMBL23397441 | 1.00 | CA5A (0.75) | CA5ACA5BTSHRCA2CA1 | |
| Sulfuric Acid SCHEMBL27972495 | 0.94 | — | — | |
| Sulfuric Acid SCHEMBL27972737 | 0.94 | — | — | |
| Sulfuric Acid SCHEMBL8546516 | 0.94 | CA5A (0.86) | CA5ACA5BTSHRCA2CA1 | |
| Sulfuric Acid SCHEMBL6368575 | 0.94 | CA5A (0.86) | CA5ACA5BTSHRCA2CA1 | |
| Sulfuric Acid SCHEMBL8620979 | 0.94 | CA5A (0.86) | CA5ACA5BTSHRCA2CA1 | |
| Sulfuric Acid SCHEMBL20597917 | 0.94 | CA5A (0.86) | CA5ACA5BTSHRCA2CA1 |
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 23 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119977330-A | Crystal greening colored glaze and preparation method thereof | 醴陵市和兴瓷业有限公司 | 2025-05-13 | — | — | CN | claimed |
| CN-114289042-B | Mesoporous solid acid catalyst, preparation method and application thereof | 万华化学集团股份有限公司 | 2023-05-30 | — | — | CN | claimed |
| CN-119977330-A | Crystal greening colored glaze and preparation method thereof | 醴陵市和兴瓷业有限公司 | 2025-05-13 | — | — | CN | disclosed |
| CN-113373521-B | Lanthanum hydroxide nanowhisker and preparation method and application thereof | 包头稀土研究院 | 2024-03-29 | — | — | CN | disclosed |
| CN-117582989-A | Synchronous and efficient removal of organic sulfur and H 2 Preparation method of S bifunctional aluminum-based desulfurization catalyst | 烟台先进材料与绿色制造山东省实验室 | 2024-02-23 | — | — | CN | disclosed |
| CN-110229124-B | Catalytic system for efficiently preparing 5-hydroxymethylfurfural and application thereof | 济南大学 | 2024-01-02 | — | — | CN | disclosed |
| CN-111359618-B | Catalyst, preparation method and application thereof, and method for catalyzing ester hydrogenation reaction | 上海亚铂化工科技有限公司 | 2022-10-25 | — | — | CN | disclosed |
| US-11260369-B2 | Catalytic composition, method of making and catalytic application thereof for producing ester(s) of glycerol | BHARAT PETROLEUM CORPORATION LIMITED (IN) | 2022-03-01 | — | — | US | disclosed |
| CN-111682200-B | Positive electrode material for lithium ion battery and preparation method thereof | 万华化学集团股份有限公司 | 2021-10-22 | — | — | CN | disclosed |
| CN-113373521-A | Lanthanum hydroxide nano whisker and preparation method and application thereof | 包头稀土研究院 | 2021-09-10 | — | — | CN | disclosed |
| CN-111235624-B | Lanthanum hydroxide nano whisker and preparation method and application thereof | 包头稀土研究院 | 2021-09-03 | — | — | CN | disclosed |
| CN-111235624-A | Lanthanum hydroxide nano whisker and preparation method and application thereof | 包头稀土研究院 | 2020-06-05 | — | — | CN | disclosed |
| US-20190002302-A1 | Hydrate of Rare Earth Metal Sulfate, Method for Producing Same, and Chemical Thermal Storage Material | KYOTO UNIVERSITY (JP) | 2019-01-03 | — | — | US | disclosed |
| US-20160158729-A1 | CATALYTIC COMPOSITION, METHOD OF MAKING AND CATALYTIC APPLICATION THEREOF FOR PRODUCING ESTER(S) OF GLYCEROL | BHARAT PETROLEUM CORPORATION LIMITED (IN) | 2016-06-09 | — | — | US | disclosed |
| US-8603939-B2 | Amide compound production catalyst, and process for production of amide compound | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2013-12-10 | — | — | US | disclosed |
| US-20130041179-A1 | AMIDE COMPOUND PRODUCTION CATALYST, AND PROCESS FOR PRODUCTION OF AMIDE COMPOUND | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2013-02-14 | — | — | US | disclosed |
| US-8129305-B2 | Oxidative reforming of low molecular weight hydrocarbons; controlling gas flow | HRD CORPORATION (US) | 2012-03-06 | — | — | US | disclosed |
| EP-2152408-A2 | CATALYST AND METHOD FOR CONVERTING NATURAL GAS TO HIGHER CARBON COMPOUNDS | HRD Corp (US) | 2010-02-17 | — | — | EP | disclosed |
| US-20080281136-A1 | CATALYST AND METHOD FOR CONVERTING NATURAL GAS TO HIGHER CARBON COMPOUNDS | HRD CORP. (US) | 2008-11-13 | — | — | US | disclosed |
| WO-2008134484-A2 | CATALYST AND METHOD FOR CONVERTING NATURAL GAS TO HIGHER CARBON COMPOUNDS | HRD CORP. (US) | 2008-11-06 | — | — | WO | 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 (2 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20160158729-A1 | CATALYTIC COMPOSITION, METHOD OF MAKING AND CATALYTIC APPLICATION THEREOF FOR PRODUCING ESTER(S) OF GLYCEROL | MGLL, AGL, GK | CA5A 652/4885CA5B 810/4885TSHR 4681/4885 |
| US-11260369-B2 | Catalytic composition, method of making and catalytic application thereof for producing ester(s) of glycerol | MGLL, AGL, GK | CA5A 652/4885CA5B 810/4885TSHR 4681/4885 |
“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.