Predicted protein targets (top 4)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ADRB1 | P08588 | 1/20 | 0.49 |
| ▸ | HTR2A | P28223 | 1/20 | 0.49 |
| ▸ | HTR2B | P41595 | 1/20 | 0.49 |
| ▸ | SIGMAR1 | Q99720 | 1/20 | 0.49 |
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 | |
|---|---|---|---|---|
| SCHEMBL1838455 | 0.95 | ADRB1 (0.48) | ADRB1HTR2AHTR2BSIGMAR1 | |
| SCHEMBL1837158 | 0.94 | ALDH1A1 (0.48) | ADRB1HTR2AHTR2BSIGMAR1 | |
| SCHEMBL1840538 | 0.94 | ALDH1A1 (0.48) | ADRB1HTR2AHTR2BSIGMAR1 | |
| SCHEMBL1838922 | 0.94 | ALDH1A1 (0.48) | ADRB1HTR2AHTR2BSIGMAR1 | |
| Ammonia Solution, Strong SCHEMBL27725772 | 0.92 | ALDH1A1 (0.47) | ADRB1HTR2AHTR2BSIGMAR1 | |
| SCHEMBL1835163 | 0.90 | ADRB1 (0.51) | ADRB1HTR2AHTR2BSIGMAR1 | |
| SCHEMBL1836929 | 0.87 | POLB (0.49) | — | |
| SCHEMBL1836927 | 0.87 | POLB (0.49) | — | |
| SCHEMBL6666615 | 0.85 | PABPC1 (0.50) | — | |
| SCHEMBL17844777 | 0.85 | HTR2A (0.52) | HTR2A |
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 47 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2025077996-A1 | SYNTHETIC PROCESS FOR THE MANUFACTURE OF ECTEINASCIDIN COMPOUNDS | PHARMA MAR, S.A. (ES) | 2025-04-17 | — | — | WO | disclosed |
| EP-3795561-B1 | METHOD FOR PRODUCING CARBAMATE AND METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2024-11-06 | — | — | EP | disclosed |
| CN-112020493-B | Method for producing urethane and method for producing isocyanate | 旭化成株式会社 | 2023-04-21 | — | — | CN | disclosed |
| EP-4138923-A1 | DRUG ANTIBODY CONJUGATES | Pharma Mar, S.A. (ES) | 2023-03-01 | — | — | EP | disclosed |
| EP-3838892-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2022-10-12 | — | — | EP | disclosed |
| US-11352319-B2 | Method for producing carbamate and method for producing isocyanate | ASAHI KASEI KABUSHIKI KAISHA (JP) | 2022-06-07 | — | — | US | disclosed |
| CN-109803992-B | Isocyanate composition and method for producing isocyanate polymer | 旭化成株式会社 | 2022-05-24 | — | — | CN | disclosed |
| CN-109843963-B | Isocyanate composition, method for producing isocyanate polymer, and isocyanate polymer | 旭化成株式会社 | 2022-05-13 | — | — | CN | disclosed |
| CN-107963982-B | Polyisocyanate composition and isocyanate polymer composition | 旭化成株式会社 | 2021-11-12 | — | — | CN | disclosed |
| EP-3293173-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2021-07-28 | — | — | EP | 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 |
| WO-2010115709-A1 | A TEXTILE PRODUCT (E.G. AN INSECTICIDE NET) | INTELLIGENT INSECT CONTROL (FR) | 2010-10-14 | — | — | WO | disclosed |
| WO-2010046348-A1 | TEXTILE PRODUCT FOR KILLING INSECTS | INTELLIGENT INSECT CONTROL (FR) | 2010-04-29 | — | — | WO | disclosed |
| CN-1173925-C | Process for preparation of carbonates and polycarbonates | 索罗蒂亚公司 | 2004-11-03 | — | — | CN | disclosed |
| CN-1059435-C | Process for preparing carbamate and its polymer | MONSANTO CO (US) | 2000-12-13 | — | — | CN | disclosed |
| CN-1047936-C | Method for producing pharmaceutical composite containing alkylmelatonins | LILLY CO ELI (US) | 2000-01-05 | — | — | CN | disclosed |
| WO-1994008952-A1 | PREPARATION OF URETHANE AND CARBONATE PRODUCTS | MONSANTO COMPANY (US) | 1994-04-28 | — | — | WO | disclosed |
| US-5302717-A | Preparation of urethane and carbonate products | MONSANTO COMPANY (US) | 1994-04-12 | — | — | US | disclosed |
| CN-1064807-A | Preparation contains the method for the pharmaceutical composition of Alkylmelatonins | LILLY CO ELI (US) | 1992-09-30 | — | — | CN | 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 (2 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-11352319-B2 | Method for producing carbamate and method for producing isocyanate | CPS1, CA7, CA4 | ADRB1 4796/4885HTR2A 3864/4885HTR2B 3350/4885 |
| 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 | ADRB1 4315/4885HTR2A 2971/4885HTR2B 2622/4885 |
“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.