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 | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 3/20 | 0.83 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.83 |
| ▸ | RECQL | P46063 | 2/20 | 0.83 |
| ▸ | HPGD | P15428 | 2/20 | 0.45 |
| ▸ | HIF1A | Q16665 | 2/20 | 0.45 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.45 |
| ▸ | LMNA | P02545 | 1/20 | 0.45 |
| ▸ | CYTH2 | Q99418 | 3/20 | 0.40 |
| ▸ | RIPK2 | O43353 | 2/20 | 0.39 |
| ▸ | RET | P07949 | 2/20 | 0.39 |
| ▸ | KDR | P35968 | 1/20 | 0.39 |
| ▸ | MAPK14 | Q16539 | 1/20 | 0.39 |
| ▸ | PKMYT1 | Q99640 | 1/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.39 |
| ▸ | ACHE | P22303 | 1/20 | 0.39 |
| ▸ | TP53 | P04637 | 1/20 | 0.39 |
| ▸ | THRB | P10828 | 1/20 | 0.39 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.39 |
| ▸ | CASP1 | P29466 | 1/20 | 0.39 |
| ▸ | GAA | P10253 | 5/20 | 0.37 |
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 | |
|---|---|---|---|---|
| SCHEMBL126869 | 0.91 | TSHR (1.00) | TSHRCYP3A4RECQLHPGDHIF1A | |
| Potassium SCHEMBL30495501 | 0.89 | TSHR (0.96) | TSHRCYP3A4RECQLHPGDHIF1A | |
| SCHEMBL28530092 | 0.89 | TSHR (0.96) | TSHRCYP3A4RECQLHPGDHIF1A | |
| Potassium SCHEMBL30495500 | 0.89 | TSHR (0.96) | TSHRCYP3A4RECQLHPGDHIF1A | |
| Sulfuric Acid SCHEMBL3329752 | 0.83 | CYP3A4 (0.57) | TSHRCYP3A4RECQLHPGDHIF1A | |
| Phenol SCHEMBL28238632 | 0.83 | TSHR (0.83) | TSHRCYP3A4RECQLHSD17B10LMNA | |
| SCHEMBL6660835 | 0.79 | CYP3A4 (0.56) | TSHRCYP3A4RECQLLMNAALDH1A1 | |
| SCHEMBL25396737 | 0.78 | CYP3A4 (0.54) | TSHRCYP3A4RECQLHPGDHIF1A | |
| SCHEMBL2743946 | 0.78 | CYP3A4 (0.54) | TSHRCYP3A4RECQLHPGDHIF1A | |
| SCHEMBL27925196 | 0.77 | CYP3A4 (0.73) | TSHRCYP3A4RECQLACHE |
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 124 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12583876-B2 | Branched organosilicon compound, method of preparing same, and related compositions | DOW SILICONES CORPORATION (US) | 2026-03-24 | — | — | US | disclosed |
| EP-3493878-B1 | COSMETIC COMPOSITION COMPRISING CURED SILICONE MATERIALS | DOW SILICONES CORP (US) | 2025-10-08 | — | — | EP | disclosed |
| US-12398270-B2 | Acrylate-functional branched organosilicon compound, method of preparing same, and copolymer formed therewith | DOW SILICONES CORPORATION (US) | 2025-08-26 | — | — | US | disclosed |
| US-12371535-B2 | Branched organosilicon compound, method of preparing same, and copolymer formed therewith | DOW SILICONES CORPORATION (US) | 2025-07-29 | — | — | US | disclosed |
| US-12338259-B2 | Branched organosilicon compound, method of preparing same, and copolymer formed therewith | DOW SILICONES CORPORATION (US) | 2025-06-24 | — | — | US | disclosed |
| US-12269833-B2 | Branched organosilicon compound, method of preparing same, and compositions comprising same | DOW SILICONES CORPORATION (US) | 2025-04-08 | — | — | US | disclosed |
| US-12215198-B2 | Branched organosilicon compound, method of preparing same, and compositions comprising same | DOW SILICONES CORPORATION (US) | 2025-02-04 | — | — | US | disclosed |
| US-20240245600-A1 | ORRIS ROOT EXTRACTS, COMPOSITIONS, AND METHODS FOR SKIN APPLICATIONS | ACCESS BUSINESS GROUP INT LLC (US) | 2024-07-25 | — | — | US | disclosed |
| US-11986547-B2 | Cosmetic composition comprising silicone materials | DOW SILICONES CORPORATION (US) | 2024-05-21 | — | — | US | disclosed |
| CN-117794504-A | Iris root extract, compositions and methods for dermatological use | 捷通国际有限公司 | 2024-03-29 | — | — | CN | disclosed |
| WO-2014081939-A1 | COSMETIC COMPOSITION COMPRISING BI-MODAL EMULSION | DOW CORNING CORPORATION (US) | 2014-05-30 | — | — | WO | disclosed |
| WO-2014081950-A2 | FABRIC CARE COMPOSITIONS COMPRISING EMULSIONS | DOW CORNING CORPORATION (US) | 2014-05-30 | — | — | WO | disclosed |
| US-20140127140-A1 | Cosmetic Composition Comprising Hydrophilic Organosilanes | DOW CORNING CORPORATION (US) | 2014-05-08 | — | — | US | disclosed |
| WO-2014070639-A2 | COSMETIC COMPOSITION COMPRISING HYDROPHILIC ORGANOSILANES | DOW CORNING CORPORATION (US) | 2014-05-08 | — | — | WO | disclosed |
| US-20130336909-A1 | PERSONAL CARE AND HEALTH CARE COMPOSITIONS | DOW CORNING CORPORATION (US) | 2013-12-19 | — | — | US | disclosed |
| EP-2663279-A2 | PERSONAL CARE COMPOSITIONS | Dow Corning Corporation (US) | 2013-11-20 | — | — | EP | disclosed |
| WO-2012095399-A2 | PERSONAL CARE AND HEALTH CARE COMPOSITIONS | DOW CORNING CORPORATION (US) | 2012-07-19 | — | — | WO | disclosed |
| US-20100143274-A1 | USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS | CIBA CORPORATION (US) | 2010-06-10 | — | — | US | disclosed |
| EP-2120846-A2 | USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS | BASF SE (DE) | 2009-11-25 | — | — | EP | disclosed |
| WO-2008107347-A2 | USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS | BASF SE (CH) | 2008-09-12 | — | — | 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 (6 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-12215198-B2 | Branched organosilicon compound, method of preparing same, and compositions comprising same | ORC3, OXSR1, OR10J3 | TSHR 933/4885CYP3A4 1394/4885RECQL 32/4885 |
| US-20100143274-A1 | USE OF AMINES AND AMIDES FOR THE STABILIZATION OF ORGANIC MICRONIZED UV ABSORBERS | MAOA, MAOB, ACMSD | TSHR 2456/4885CYP3A4 360/4885RECQL 774/4885 |
| US-12583876-B2 | Branched organosilicon compound, method of preparing same, and related compositions | OXSR1, BRS3, NPSR1 | TSHR 172/4885CYP3A4 931/4885RECQL 2377/4885 |
| US-12269833-B2 | Branched organosilicon compound, method of preparing same, and compositions comprising same | NR3C2, NR2E3, OXER1 | TSHR 376/4885CYP3A4 1926/4885RECQL 2805/4885 |
| US-12338259-B2 | Branched organosilicon compound, method of preparing same, and copolymer formed therewith | OXSR1, BRS3, ORC3 | TSHR 887/4885CYP3A4 1716/4885RECQL 1276/4885 |
| US-12371535-B2 | Branched organosilicon compound, method of preparing same, and copolymer formed therewith | OXSR1, BRS3, OXER1 | TSHR 187/4885CYP3A4 1178/4885RECQL 1748/4885 |
“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.