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 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.41 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.41 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.36 |
| ▸ | MAPT | P10636 | 2/20 | 0.35 |
| ▸ | TSHR | P16473 | 2/20 | 0.35 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.35 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.35 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.35 |
| ▸ | LMNA | P02545 | 1/20 | 0.35 |
| ▸ | GAA | P10253 | 1/20 | 0.35 |
| ▸ | PKM | P14618 | 1/20 | 0.35 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.35 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.35 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.35 |
| ▸ | FNTA | P49354 | 1/20 | 0.34 |
| ▸ | FNTB | P49356 | 1/20 | 0.34 |
| ▸ | HTT | P42858 | 1/20 | 0.34 |
| ▸ | FDPS | P14324 | 2/20 | 0.33 |
| ▸ | ADAM17 | P78536 | 1/20 | 0.33 |
| ▸ | LPO | P22079 | 1/20 | 0.32 |
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 | |
|---|---|---|---|---|
| SCHEMBL27998888 | 0.98 | L3MBTL1 (0.42) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| Bromide SCHEMBL28320357 | 0.97 | L3MBTL1 (0.41) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| Hydrochloric Acid SCHEMBL29043668 | 0.97 | L3MBTL1 (0.41) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| SCHEMBL27998576 | 0.94 | L3MBTL1 (0.40) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| SCHEMBL28415731 | 0.92 | L3MBTL1 (0.39) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| Cyanide SCHEMBL28324913 | 0.92 | L3MBTL1 (0.39) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| Trifluoromethanesulfonic Acid SCHEMBL28492046 | 0.90 | KMT2A (0.39) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| Sulfuric Acid SCHEMBL28489606 | 0.88 | L3MBTL1 (0.40) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| Trifluoroacetic Acid SCHEMBL28489578 | 0.87 | KMT2A (0.43) | L3MBTL1KDM4ECYP2D6MAPTTSHR | |
| SCHEMBL16570039 | 0.86 | L3MBTL1 (0.39) | L3MBTL1KDM4ECYP2D6MAPTTSHR |
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 12 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117327034-A | Method for preparing 5-hydroxymethylfurfural by catalyzing passion fruit shells through sulfonated ionic liquid | 集美大学 | 2024-01-02 | — | — | CN | claimed |
| CN-116178315-A | Method for efficiently converting chitosan into 5-hydroxymethylfurfural by using sulfonated ionic liquid | 集美大学 | 2023-05-30 | — | — | CN | claimed |
| CN-117772274-A | Ion liquid modified rare earth doped solid acid catalyst and preparation method thereof | 江苏扬农化工集团有限公司 | 2024-03-29 | — | — | CN | disclosed |
| CN-117327034-A | Method for preparing 5-hydroxymethylfurfural by catalyzing passion fruit shells through sulfonated ionic liquid | 集美大学 | 2024-01-02 | — | — | CN | disclosed |
| CN-116082540-B | Synthesis process of low-volatile odorless polyvinyl butyral resin powder | 江苏奥天利新材料有限公司 | 2023-09-26 | — | — | CN | disclosed |
| CN-116283568-A | Preparation method of sorbate | 南通新宙邦电子材料有限公司 | 2023-06-23 | — | — | CN | disclosed |
| CN-116178315-A | Method for efficiently converting chitosan into 5-hydroxymethylfurfural by using sulfonated ionic liquid | 集美大学 | 2023-05-30 | — | — | CN | disclosed |
| CN-111995653-B | Preparation method of phytosterol/stanol ferulate | 江苏大学 | 2023-05-30 | — | — | CN | disclosed |
| CN-116082540-A | Synthesis process of low-volatile odorless polyvinyl butyral resin powder | 江苏奥天利新材料有限公司 | 2023-05-09 | — | — | CN | disclosed |
| CN-111057007-B | Functionalized ionic liquid based on dual-core structure, preparation method thereof and use method of functionalized ionic liquid for degrading lignocellulose | 东北农业大学 | 2023-01-17 | — | — | CN | disclosed |
| CN-111995653-A | Preparation method of phytosterol/stanol ferulic acid ester | 江苏大学 | 2020-11-27 | — | — | CN | disclosed |
| CN-107722033-B | Method for separating sugar alcohol dehydration reaction product by adding hydrophobic ionic liquid and carrying out reduced pressure distillation | 上海纳米技术及应用国家工程研究中心有限公司 | 2020-06-02 | — | — | CN | disclosed |