Predicted protein targets (top 8)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.56 |
| ▸ | TSHR | P16473 | 3/20 | 0.47 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.47 |
| ▸ | MEN1 | O00255 | 1/20 | 0.36 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.36 |
| ▸ | CA5A | P35218 | 1/20 | 0.33 |
| ▸ | CA5B | Q9Y2D0 | 1/20 | 0.33 |
| ▸ | LMNA | P02545 | 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 | |
|---|---|---|---|---|
| Sulfuric Acid SCHEMBL17180589 | 0.84 | ALDH1A1 (0.43) | ALDH1A1TSHRTDP1MEN1KMT2A | |
| SCHEMBL1122744 | 0.78 | — | — | |
| SCHEMBL1330527 | 0.78 | — | — | |
| Hydrochloric Acid SCHEMBL29395602 | 0.77 | ALDH1A1 (0.43) | ALDH1A1TSHRTDP1 | |
| Ammonia Solution, Strong SCHEMBL14248697 | 0.75 | — | — | |
| SCHEMBL3635527 | 0.75 | — | — | |
| SCHEMBL1119156 | 0.75 | — | — | |
| SCHEMBL3306963 | 0.75 | ALDH1A1 (0.56) | ALDH1A1TSHRTDP1MEN1KMT2A | |
| SCHEMBL1170452 | 0.75 | ALDH1A1 (0.41) | ALDH1A1TSHRTDP1 | |
| SCHEMBL27296549 | 0.74 | — | — |
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 566 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120190188-A | Method for synchronously promoting dissolution of oil-containing iron mud and rapid separation of iron in dissolution liquid | 绿尔盛(重庆)环境科技有限公司 | 2025-06-24 | — | — | CN | claimed |
| US-20250092082-A1 | PHOTON GENERATING SUBSTRATES FOR OLIGONUCLEOTIDE SYNTHESIS | MICROSOFT TECHNOLOGY LICENSING, LLC | 2025-03-20 | — | — | US | claimed |
| CN-119019376-A | Imidazole-based nitroxide free radical controllable synthesis method and application thereof | 华东师范大学 | 2024-11-26 | — | — | CN | claimed |
| WO-2024143106-A1 | STABILIZED ALKYL-BROMIDE-COMPOUND-CONTAINING LIQUID COMPOSITION AND USE FOR SAME | 東ソー株式会社 | 2024-07-04 | — | — | WO | claimed |
| US-11965068-B2 | Cross-linked polymer networks and methods of making and using same | CORNELL UNIVERSITY (US) | 2024-04-23 | — | — | US | claimed |
| EP-3565484-B1 | COMPOSITIONS FOR IMPLANTING AND REVERSING STIMULI-RESPONSIVE IMPLANTS | CONTRALINE INC (US) | 2024-04-03 | — | — | EP | claimed |
| CN-117507081-A | Dyeing method for improving color fastness of wood and application thereof | 德华兔宝宝装饰新材股份有限公司 | 2024-02-06 | — | — | CN | claimed |
| CN-117362180-A | Method for extracting 2, 3-dimethyl-2, 3-dinitrobutane from deactivated titanium silicalite molecular sieve catalyst | 定州旭阳科技有限公司 | 2024-01-09 | — | — | CN | claimed |
| US-11833225-B2 | Methods and compositions for efficient gene deletion | CRISPR THERAPEUTICS AG (CH) | 2023-12-05 | — | — | US | claimed |
| CN-116209887-A | System and method for detecting volatile organic compounds | 纳米生物检测系统公司 | 2023-06-02 | — | — | CN | claimed |
| WO-2007108797-A2 | A METHOD OF PRODUCING ENERGETICALLY-INERT PSEUDOSCENTS OF EXPLOSIVE MATERIALS, AND COMPOSITIONS THEREOF | GMA INDUSTRIES (US) | 2007-09-27 | — | — | WO | claimed |
| WO-2007091998-A2 | METHOD AND APPARATUS FOR PRE-CONCENTRATION OF VOLATILE COMPOUNDS OF EXPLOSIVES AND TAGGANTS IN EXPLOSIVES FOR SUBSEQUENT DETECTION BY ION MOBILITY SPECTROMETRY | THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) | 2007-08-16 | — | — | WO | claimed |
| WO-2006109304-A2 | EXTREMELY INSENSITIVE DETONATING SUBSTANCE AND METHOD FOR ITS MANUFACTURE | RAFAEL ARMAMENT DEVELOPMENT AUTHORITY LTD. (IL) | 2006-10-19 | — | — | WO | claimed |
| US-6911328-B2 | Method for producing 2,3-dimethyl-2,3-dinitrobutane and product thereby | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) | 2005-06-28 | — | — | US | claimed |
| US-20040043461-A1 | Method for producing 2,3-dimethyl-2,3-dinitrobutane and product thereby | FITZGERALD ANGEL A (US) | 2004-03-04 | — | — | US | claimed |
| EP-1000011-A4 | PREPARATION OF TETRAMETHYLETHYLENEDIAMINE | HAMPSHIRE CHEMICAL CORP (US) | 2001-09-19 | — | — | EP | claimed |
| EP-1000011-A1 | PREPARATION OF TETRAMETHYLETHYLENEDIAMINE | HAMPSHIRE CHEMICAL CORPORATION (US) | 2000-05-17 | — | — | EP | claimed |
| WO-1999006350-A1 | PREPARATION OF TETRAMETHYLETHYLENEDIAMINE | HAMPSHIRE CHEMICAL CORP. (US) | 1999-02-11 | — | — | WO | claimed |
| WO-1998046544-A1 | ENCAPSULATED VAPOR-DETECTION AND IDENTIFICATION TAGS | THE DOW CHEMICAL COMPANY (US) | 1998-10-22 | — | — | WO | claimed |
| US-5811584-A | REDUCING 2,3-DIMETHYL-2,3-DINITROBUTANE WITH HYDROGEN IN PRESENCE OF CHROMIUM PROMOTED RANEY COBALT CATALYST | HAMPSHIRE CHEMICAL CORP. (US) | 1998-09-22 | — | — | US | claimed |