Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.57 |
| ▸ | PTGS2 | P35354 | 4/20 | 0.41 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.41 |
| ▸ | HCAR1 | Q9BXC0 | 1/20 | 0.41 |
| ▸ | ACHE | P22303 | 4/20 | 0.40 |
| ▸ | TRPA1 | O75762 | 1/20 | 0.39 |
| ▸ | LTA4H | P09960 | 1/20 | 0.39 |
| ▸ | CA12 | O43570 | 1/20 | 0.39 |
| ▸ | CA1 | P00915 | 1/20 | 0.39 |
| ▸ | CA2 | P00918 | 1/20 | 0.39 |
| ▸ | CA7 | P43166 | 1/20 | 0.39 |
| ▸ | CA9 | Q16790 | 1/20 | 0.39 |
| ▸ | CA14 | Q9ULX7 | 1/20 | 0.39 |
| ▸ | ALOX5 | P09917 | 1/20 | 0.38 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.38 |
| ▸ | HSD17B1 | P14061 | 1/20 | 0.38 |
| ▸ | HSD17B2 | P37059 | 1/20 | 0.38 |
| ▸ | NR1H2 | P55055 | 1/20 | 0.38 |
| ▸ | NR1H3 | Q13133 | 1/20 | 0.38 |
| ▸ | PGK1 | P00558 | 1/20 | 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 | |
|---|---|---|---|---|
| SCHEMBL31200644 | 1.00 | ALDH1A1 (0.57) | ALDH1A1PTGS2CYP3A4HCAR1ACHE | |
| SCHEMBL14134419 | 0.84 | ALDH1A1 (0.39) | ALDH1A1PTGS2TRPA1ALOX5PTGS1 | |
| SCHEMBL207718 | 0.84 | PTGS2 (0.48) | ALDH1A1PTGS2CYP3A4ACHETRPA1 | |
| SCHEMBL69634 | 0.84 | ACHE (0.55) | ALDH1A1PTGS2CYP3A4ACHETRPA1 | |
| SCHEMBL29215628 | 0.82 | ALDH1A1 (0.60) | ALDH1A1PTGS2CYP3A4HCAR1ACHE | |
| SCHEMBL30899188 | 0.82 | ALDH1A1 (0.60) | ALDH1A1PTGS2CYP3A4HCAR1ACHE | |
| SCHEMBL3959592 | 0.81 | PTGS2 (0.54) | ALDH1A1PTGS2CYP3A4HCAR1ACHE | |
| SCHEMBL5490825 | 0.81 | PGK1 (0.44) | ALDH1A1PTGS2TRPA1ALOX5PTGS1 | |
| SCHEMBL168174 | 0.81 | PGK1 (0.44) | ALDH1A1PTGS2TRPA1ALOX5PTGS1 | |
| SCHEMBL271754 | 0.81 | ALDH1A1 (0.42) | ALDH1A1PTGS2ACHETRPA1ALOX5 |
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 560 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122080054-A | Method for synthesizing tri (3, 4-methyl ethyl) phenol phosphate | — | 2026-05-26 | — | — | CN | claimed |
| CN-122011307-A | Method for synthesizing phenolic resin from 2,4/2, 5-methyl ethyl phenol | 煤炭科学技术研究院有限公司 | 2026-05-12 | — | — | CN | claimed |
| CN-122011306-A | Method for synthesizing phenolic resin from mixed phenol containing 2,4, 6-tricresyl | 煤炭科学技术研究院有限公司 | 2026-05-12 | — | — | CN | claimed |
| CN-113396171-B | Process for producing polyphenol derivative, and resin composition containing polyphenol derivative | 出光兴产株式会社 | 2025-03-28 | — | — | CN | claimed |
| CN-119490388-A | Method for separating and obtaining phenolic substances from phenol-containing coal tar | 煤炭科学技术研究院有限公司 | 2025-02-21 | — | — | CN | claimed |
| CN-119431113-A | Method for refining 2,3, 5-tricresyl and 3-methyl-5-ethylphenol from trimethylphenol mixture | 煤炭科学技术研究院有限公司 | 2025-02-14 | — | — | CN | claimed |
| CN-119431115-A | Impurity removing method for mixed phenol extracted from coal tar | 煤炭科学技术研究院有限公司 | 2025-02-14 | — | — | CN | claimed |
| CN-119060278-A | Method for synthesizing photoresist by using m-p-ethyl phenol mixture | 盐城工学院 | 2024-12-03 | — | — | CN | claimed |
| US-20240376284-A1 | Method for Screening Solvent for Acrylonitrile Butadiene Styrene Copolymer Extraction, Recycling Method for Waste Material, and Recycled Acrylonitrile Butadiene Styrene Copolymer and Composition | LG CHEM, LTD. (KR) | 2024-11-14 | — | — | US | claimed |
| US-20240376285-A1 | Method for Screening Solvent for Extracting Acrylonitrile Butadiene Styrene Copolymer, Method for Recycling Waste, Recycled Acrylonitrile Butadiene Styrene Copolymer, and Composition | LG CHEM, LTD. (KR) | 2024-11-14 | — | — | US | claimed |
| WO-2001077079-A2 | POLYCYCLIC ARYL AND HETEROARYL SUBSTITUTED 4-PYRIDONES USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE | PHARMACIA CORPORATION (US) | 2001-10-18 | — | — | WO | claimed |
| WO-2001077097-A2 | POLYCYCLIC ARYL AND HETEROARYL SUBSTITUTED 4-PYRONES USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE | PHARMACIA CORPORATION (US) | 2001-10-18 | — | — | WO | claimed |
| WO-2001068605-A1 | POLYCYCLIC ARYL AND HETEROARYL SUBSTITUTED BENZENES USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE | PHARMACIA CORPORATION (US) | 2001-09-20 | — | — | WO | claimed |
| US-20010018446-A1 | Substituted N-Aliphatic-N-Aromatictertiary-Heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity | G.D. SEARLE & CO. (US) | 2001-08-30 | — | — | US | claimed |
| EP-1115695-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(N+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | claimed |
| EP-1115693-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL $i(TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | claimed |
| EP-1115694-A1 | SUBSTITUTED N-ALIPHATIC-N-AROMATIC (TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | claimed |
| WO-2000018724-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(n+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | claimed |
| WO-2000018723-A1 | SUBSTITUTED N-ALIPHATIC-N-AROMATIC TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | claimed |
| WO-2000018721-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (1 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-20010018446-A1 | Substituted N-Aliphatic-N-Aromatictertiary-Heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity | CETP, DBI, MTTP | ALDH1A1 2624/4885PTGS2 4509/4885CYP3A4 2162/4885 |
“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.