Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | HSD17B10 | Q99714 | 8/20 | 0.91 |
| ▸ | TSHR | P16473 | 7/20 | 0.91 |
| ▸ | HPGD | P15428 | 7/20 | 0.91 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.91 |
| ▸ | MEN1 | O00255 | 2/20 | 0.91 |
| ▸ | LMNA | P02545 | 2/20 | 0.91 |
| ▸ | MAPT | P10636 | 2/20 | 0.91 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.91 |
| ▸ | CYP1A2 | P05177 | 4/20 | 0.50 |
| ▸ | CYP2C9 | P11712 | 4/20 | 0.50 |
| ▸ | HIF1A | Q16665 | 3/20 | 0.50 |
| ▸ | CASP1 | P29466 | 1/20 | 0.47 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.43 |
| ▸ | MAPK1 | P28482 | 3/20 | 0.42 |
| ▸ | CYP3A4 | P08684 | 5/20 | 0.40 |
| ▸ | USP2 | O75604 | 1/20 | 0.40 |
| ▸ | TP53 | P04637 | 1/20 | 0.40 |
| ▸ | GLA | P06280 | 1/20 | 0.40 |
| ▸ | THRB | P10828 | 1/20 | 0.40 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.40 |
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 | |
|---|---|---|---|---|
| Pentachlorophenol SCHEMBL5315995 | 0.95 | HSD17B10 (1.00) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL23121452 | 0.95 | HSD17B10 (1.00) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Perchlorobenzene SCHEMBL28269084 | 0.95 | HSD17B10 (1.00) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL1492 | 0.95 | HSD17B10 (1.00) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL1330735 | 0.95 | HSD17B10 (1.00) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL21177789 | 0.91 | HSD17B10 (0.91) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL41162 | 0.91 | HSD17B10 (0.91) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL21647360 | 0.91 | HSD17B10 (0.91) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL22027593 | 0.91 | HSD17B10 (0.91) | HSD17B10TSHRHPGDALDH1A1MEN1 | |
| Pentachlorophenol SCHEMBL11459279 | 0.91 | HSD17B10 (0.91) | HSD17B10TSHRHPGDALDH1A1MEN1 |
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 14 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114848840-A | Modified iron-based nano material, iron-based nano liposome and anti-tumor application thereof | 北京福纳康生物技术有限公司 | 2022-08-05 | — | — | CN | claimed |
| CN-114848840-B | Modified iron-based nano material, iron-based nano liposome and antitumor application thereof | 北京福纳康生物技术有限公司 | 2023-08-29 | — | — | CN | disclosed |
| CN-114848840-A | Modified iron-based nano material, iron-based nano liposome and anti-tumor application thereof | 北京福纳康生物技术有限公司 | 2022-08-05 | — | — | CN | disclosed |
| CN-111760874-B | Fine separation method of carbide slag iron and application thereof | 武汉理工大学 | 2022-07-08 | — | — | CN | disclosed |
| CN-111760874-A | Fine separation method of carbide slag iron and application thereof | 武汉理工大学 | 2020-10-13 | — | — | CN | disclosed |
| EP-1773282-A2 | FRAGRANCE FRIENDLY AND COST EFFECTIVE ANTIPERSPIRANT ACTIVES | REHEIS, INC. (US) | 2007-04-18 | — | — | EP | disclosed |
| US-7153495-B2 | Fragrance friendly and cost effective antiperspirant actives and method of making the same | REHEIS, INC. (US) | 2006-12-26 | — | — | US | disclosed |
| WO-2006001839-A2 | FRAGRANCE FRIENDLY AND COST EFFECTIVE ANTIPERSPIRANT ACTIVES | REHEIS, INC. (US) | 2006-01-05 | — | — | WO | disclosed |
| US-20050276773-A1 | Fragrance friendly and cost effective antiperspirant actives and method of making the same | REHEIS, INC. | 2005-12-15 | — | — | US | disclosed |
| WO-1999039575-A9 | SYNERGISTIC BIOCIDAL ACTIVITY OF TERNARY COMPLEXES OF NEGATIVELY -CHARGED BIOCIDES (COMPONENT A), TRANSITION METAL IONS (COMPONENT B), AND NEUTRAL CHELATORS (COMPONENT C) | YISSUM RES DEV CO (IL) | 1999-10-21 | — | — | WO | disclosed |
| WO-1999039575-A2 | SYNERGISTIC BIOCIDAL ACTIVITY OF TERNARY COMPLEXES OF NEGATIVELY -CHARGED BIOCIDES (COMPONENT A), TRANSITION METAL IONS (COMPONENT B), AND NEUTRAL CHELATORS (COMPONENT C) | YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM (IL) | 1999-08-12 | — | — | WO | disclosed |
| EP-0382472-A2 | Ring-contracted macrolides | ELI LILLY AND COMPANY (US) | 1990-08-16 | — | — | EP | disclosed |
| EP-0378228-A2 | Propheromones, their preparation, and their use for long-term pheromone release | CESKOSLOVENSKA AKADEMIE VED (CS) | 1990-07-18 | — | — | EP | disclosed |
| EP-0141561-B1 | A PROCESS FOR PRODUCING DEVICES HAVING SEMI-INSULATING INDIUM PHOSPHIDE BASED COMPOSITIONS | AT&T Corp. (US) | 1989-07-26 | — | — | EP | disclosed |