Predicted protein targets (top 13)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | FAAH | O00519 | 5/20 | 0.59 |
| ▸ | CNR1 | P21554 | 1/20 | 0.57 |
| ▸ | CNR2 | P34972 | 1/20 | 0.57 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.55 |
| ▸ | GPR84 | Q9NQS5 | 7/20 | 0.50 |
| ▸ | ACE2 | Q9BYF1 | 1/20 | 0.50 |
| ▸ | FFAR1 | O14842 | 1/20 | 0.50 |
| ▸ | MAPT | P10636 | 1/20 | 0.48 |
| ▸ | LCK | P06239 | 1/20 | 0.48 |
| ▸ | PPARD | Q03181 | 1/20 | 0.48 |
| ▸ | ZDHHC20 | Q5W0Z9 | 1/20 | 0.48 |
| ▸ | ZDHHC2 | Q9UIJ5 | 1/20 | 0.48 |
| ▸ | LMNA | P02545 | 2/20 | 0.47 |
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 | |
|---|---|---|---|---|
| SCHEMBL1835355 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1840168 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1839719 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1840086 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1837153 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1837219 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1836768 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1833842 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL654708 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 | |
| SCHEMBL1837800 | 1.00 | FAAH (0.59) | FAAHCNR1CNR2ALDH1A1GPR84 |
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 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122055369-A | Bridged tricyclic carbamoyl pyridone compounds and uses thereof | 吉利德科学公司 | 2026-05-15 | — | — | CN | disclosed |
| CN-116891465-A | N-substituted quinolinone compounds, preparation method and application thereof | 苏州旺山旺水生物医药有限公司 | 2023-10-17 | — | — | CN | disclosed |
| CN-108463481-B | Method for producing polycarbonate | 国际壳牌研究有限公司 | 2021-04-09 | — | — | CN | disclosed |
| CN-108473672-B | Process for preparing melt polycarbonate | 国际壳牌研究有限公司 | 2020-12-08 | — | — | CN | disclosed |
| US-10654973-B2 | Method for producing polycarbonate | SHELL OIL COMPANY (US) | 2020-05-19 | — | — | US | disclosed |
| US-10640609-B2 | Method for preparing a melt polycarbonate | SHELL OIL COMPANY (US) | 2020-05-05 | — | — | US | disclosed |
| EP-3394146-B1 | METHOD FOR PREPARING A MELT POLYCARBONATE | SHELL INT RESEARCH (NL) | 2019-10-30 | — | — | EP | disclosed |
| EP-3394149-B1 | METHOD FOR PRODUCING POLYCARBONATE | SHELL INT RESEARCH (NL) | 2019-10-30 | — | — | EP | disclosed |
| US-20190010281-A1 | METHOD FOR PRODUCING POLYCARBONATE OLIGOMERS | SHELL OIL COMPANY | 2019-01-10 | — | — | US | disclosed |
| US-20180371164-A1 | METHOD FOR PRODUCING POLYCARBONATE | SHELL OIL COMPANY (US) | 2018-12-27 | — | — | US | disclosed |
| US-9249090-B2 | N-substituted carbamic acid ester production method and isocyanate production method using the N-substituted carbamic acid ester | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2016-02-02 | — | — | US | disclosed |
| US-9145357-B2 | N-substituted carbamic acid ester production method, isocyanate production method using such N-substituted carbamic acid ester, and composition for transfer and storage of N-substituted carbamic acid ester comprising N-substituted carbamic acid ester and aromatic hydroxy compound | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2015-09-29 | — | — | US | disclosed |
| US-20150038742-A1 | N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2015-02-05 | — | — | US | disclosed |
| US-8884047-B2 | N-substituted carbamic acid ester production method and isocyanate production method using the N-substituted carbamic acid ester | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2014-11-11 | — | — | US | disclosed |
| US-20140194650-A1 | N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, and Composition for Transfer and Storage of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2014-07-10 | — | — | US | disclosed |
| US-8658819-B2 | N-substituted carbamic acid ester production method, isocyanate production method using such N-substituted carbamic acid ester, and composition for transfer and storage of N-substituted carbamic acid ester comprising N-substituted carbamic acid ester and aromatic hydroxy compound | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2014-02-25 | — | — | US | disclosed |
| US-20110160476-A1 | N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2011-06-30 | — | — | US | disclosed |
| US-20110133121-A1 | N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, And Composition For Transfer And Storage Of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2011-06-09 | — | — | US | disclosed |
| EP-2322504-A1 | PROCESS FOR THE PREPARATION OF N-SUBSTITUTED CARBAMIC ACID ESTER AND PROCESS FOR THE PREPARATION OF ISOCYANATE USING THE N-SUBSTITUTED CARBAMIC ACID ESTER | Asahi Kasei Chemicals Corporation (JP) | 2011-05-18 | — | — | EP | disclosed |
| US-3931041-A | LIQUID CRYSTAL COMPOSITIONS | XEROX CORPORATION (US) | 1976-01-06 | — | — | US | 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 (5 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-20110133121-A1 | N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, And Composition For Transfer And Storage Of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound | CPS1, ALKBH3, RCC1 | FAAH 200/4885CNR1 400/4885CNR2 210/4885 |
| US-20140194650-A1 | N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, and Composition for Transfer and Storage of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound | CPS1, ALKBH3, RCC1 | FAAH 200/4885CNR1 400/4885CNR2 210/4885 |
| US-10640609-B2 | Method for preparing a melt polycarbonate | PKD1, HSD17B7, DHCR7 | FAAH 4453/4885CNR1 3211/4885CNR2 3141/4885 |
| US-20110160476-A1 | N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester | ALKBH3, CPS1, APEH | FAAH 130/4885CNR1 538/4885CNR2 427/4885 |
| US-20150038742-A1 | N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester | ALKBH3, CPS1, APEH | FAAH 130/4885CNR1 538/4885CNR2 427/4885 |
“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.