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 | |
|---|---|---|---|---|
| ▸ | MAOA known ✓ | P21397 | 1/20 | 0.31 |
| ▸ | MAOB known ✓ | P27338 | 1/20 | 0.31 |
| ▸ | CA5A | P35218 | 4/20 | 0.55 |
| ▸ | LMNA | P02545 | 4/20 | 0.55 |
| ▸ | CA5B | Q9Y2D0 | 3/20 | 0.55 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.55 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.55 |
| ▸ | OR51E2 | Q9H255 | 1/20 | 0.55 |
| ▸ | BLM | P54132 | 6/20 | 0.53 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.53 |
| ▸ | TSHR | P16473 | 5/20 | 0.46 |
| ▸ | CA2 | P00918 | 4/20 | 0.46 |
| ▸ | CA9 | Q16790 | 3/20 | 0.46 |
| ▸ | CA1 | P00915 | 2/20 | 0.46 |
| ▸ | CA4 | P22748 | 2/20 | 0.46 |
| ▸ | CA6 | P23280 | 2/20 | 0.46 |
| ▸ | CA7 | P43166 | 2/20 | 0.46 |
| ▸ | NT5E | P21589 | 1/20 | 0.46 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.42 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.42 |
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 SCHEMBL3902876 | 0.95 | CA5A (0.60) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL379310 | 0.95 | — | — | |
| Sulfuric Acid SCHEMBL145458 | 0.95 | CA5A (0.60) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL825387 | 0.91 | CA5A (0.55) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL825390 | 0.91 | CA5A (0.55) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL28735279 | 0.91 | CA5A (0.55) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL26093424 | 0.91 | CA5A (0.55) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL9238196 | 0.91 | CA5A (0.55) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL2236255 | 0.91 | CA5A (0.55) | CA5ALMNACA5BALDH1A1TDP1 | |
| Sulfuric Acid SCHEMBL27760237 | 0.91 | CA5A (0.55) | CA5ALMNACA5BALDH1A1TDP1 |
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 20 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-109503540-B | Method for preparing epsilon-caprolactone and continuous production device thereof | 黎明化工研究设计院有限责任公司 | 2023-05-05 | — | — | CN | claimed |
| CN-105503685-B | A kind of method and its device for preparing anhydrous peroxyacetic acid solution | 黎明化工研究设计院有限责任公司 | 2017-10-13 | — | — | CN | claimed |
| CN-109503540-B | Method for preparing epsilon-caprolactone and continuous production device thereof | 黎明化工研究设计院有限责任公司 | 2023-05-05 | — | — | CN | disclosed |
| CN-105503685-B | A kind of method and its device for preparing anhydrous peroxyacetic acid solution | 黎明化工研究设计院有限责任公司 | 2017-10-13 | — | — | CN | disclosed |
| CN-105503685-B | A kind of method and its device for preparing anhydrous peroxyacetic acid solution | 黎明化工研究设计院有限责任公司 | 2017-10-13 | — | — | CN | disclosed |
| CN-105503685-A | Method and device for preparing anhydrous peroxyacetic acid solution | LIMING RES INST OF CHEMICAL IND | 2016-04-20 | — | — | CN | disclosed |
| CN-105503685-A | Method and device for preparing anhydrous peroxyacetic acid solution | LIMING RES INST OF CHEMICAL IND | 2016-04-20 | — | — | CN | disclosed |
| US-7220328-B1 | Low-smoke gas generating low order pressure pulse compositions | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) | 2007-05-22 | — | — | US | disclosed |
| US-6846926-B1 | Triazolyl-aminotriazine compositions, including salts | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) | 2005-01-25 | — | — | US | disclosed |
| US-6673924-B2 | EXPLOSIVES; PYROTECHNICS; CYCLIZATION OF DICYANDIAMIDE WITH HYDRAZINE HYDROCHLORIDE | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY | 2004-01-06 | — | — | US | disclosed |
| US-6632305-B2 | Chemical intermediates for use in explosives/pyrotechnics, herbicides, pesticides, fungicides and fertilizers | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY | 2003-10-14 | — | — | US | disclosed |
| US-6602366-B2 | Metal complexes; for smokeless fireworks | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY | 2003-08-05 | — | — | US | disclosed |
| US-20030069247-A1 | 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-substituted precursor, and process, and compounds therefrom | NAVY, UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY | 2003-04-10 | — | — | US | disclosed |
| US-20030013878-A1 | 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-substituted precursor, and process, and compounds therefrom | NAVY, UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY OF | 2003-01-16 | — | — | US | disclosed |
| US-20030013877-A1 | Triazolyl-tetrazinyl-aminotriazine compounds useful in pyrotechnic compositions and process thereof | KOPPES WILLIAM M (US) | 2003-01-16 | — | — | US | disclosed |
| WO-2002098855-A2 | 1,2,4-TRIAZOLO[4,3-a][1,3,5]TRIAZINE-3,5,7-SUBSTITUTED PRECURSOR, AND PROCESS, AND COMPOUNDS THEREFROM | MCDONNELL THOMAS E (US) | 2002-12-12 | — | — | WO | disclosed |
| US-5635322-A | Process for developing and overcoating migration imaging members | XEROX CORPORTION (US) | 1997-06-03 | — | — | US | disclosed |
| US-5580689-A | SOLFTENABLE LAYER OF SOFTENABLE MATERIAL, PIGMENT SENSITIVE TO INFRARED OR RED LIGHT ILLUMINATION, AND MIGRATION MARKING MATERIAL | XEROX CORPORATION (US) | 1996-12-03 | — | — | US | disclosed |
| US-5534374-A | Migration imaging members | XEROX CORPORATION (US) | 1996-07-09 | — | — | US | disclosed |
| EP-0673781-A1 | Recording sheets containing amine salts and quaternary choline halides | XEROX CORPORATION (US) | 1995-09-27 | — | — | EP | 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 (3 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-20030069247-A1 | 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-substituted precursor, and process, and compounds therefrom | IKZF3, WEE1, CYP4Z1 | MAOA 950/4885MAOB 2238/4885CA5A 94/4885 |
| US-20030013878-A1 | 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-substituted precursor, and process, and compounds therefrom | IKZF3, WEE1, CYP4Z1 | MAOA 950/4885MAOB 2238/4885CA5A 94/4885 |
| US-20030013877-A1 | Triazolyl-tetrazinyl-aminotriazine compounds useful in pyrotechnic compositions and process thereof | KCNN2, KCNN1, AADAT | MAOA 1573/4885MAOB 1655/4885CA5A 110/4885 |
“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.