Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MAOB | P27338 | 9/20 | 1.00 |
| ▸ | CYP1B1 | Q16678 | 2/20 | 0.86 |
| ▸ | MAPT | P10636 | 4/20 | 0.75 |
| ▸ | LMNA | P02545 | 2/20 | 0.75 |
| ▸ | BCHE | P06276 | 2/20 | 0.75 |
| ▸ | PLIN1 | O60240 | 1/20 | 0.75 |
| ▸ | TNFRSF1A | P19438 | 1/20 | 0.75 |
| ▸ | ACHE | P22303 | 1/20 | 0.75 |
| ▸ | RECQL | P46063 | 1/20 | 0.75 |
| ▸ | PLIN5 | Q00G26 | 1/20 | 0.75 |
| ▸ | ABHD5 | Q8WTS1 | 1/20 | 0.75 |
| ▸ | CXCL12 | P48061 | 1/20 | 0.72 |
| ▸ | CYP3A4 | P08684 | 3/20 | 0.71 |
| ▸ | NFKB1 | P19838 | 2/20 | 0.71 |
| ▸ | NFKB2 | Q00653 | 2/20 | 0.71 |
| ▸ | RELA | Q04206 | 2/20 | 0.71 |
| ▸ | HSPD1 | P10809 | 1/20 | 0.71 |
| ▸ | PKM | P14618 | 1/20 | 0.71 |
| ▸ | RAB9A | P51151 | 1/20 | 0.71 |
| ▸ | HSPE1 | P61604 | 1/20 | 0.71 |
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 | |
|---|---|---|---|---|
| 4-Chloro Chalcone SCHEMBL197310 | 1.00 | MAOB (1.00) | MAOBCYP1B1MAPTLMNABCHE | |
| 4-Chloro Chalcone SCHEMBL198518 | 1.00 | MAOB (1.00) | MAOBCYP1B1MAPTLMNABCHE | |
| SCHEMBL196425 | 0.93 | CYP1B1 (1.00) | MAOBCYP1B1MAPTLMNABCHE | |
| SCHEMBL196424 | 0.93 | CYP1B1 (1.00) | MAOBCYP1B1MAPTLMNABCHE | |
| SCHEMBL10415521 | 0.93 | CYP1B1 (1.00) | MAOBCYP1B1MAPTLMNABCHE | |
| 4',4-Dichlorochalcone SCHEMBL659210 | 0.90 | MAOB (0.86) | MAOBCYP1B1MAPTTNFRSF1ACXCL12 | |
| 4',4-Dichlorochalcone SCHEMBL659211 | 0.90 | MAOB (0.86) | MAOBCYP1B1MAPTTNFRSF1ACXCL12 | |
| SCHEMBL9915665 | 0.90 | CYP1B1 (0.91) | MAOBCYP1B1MAPTLMNABCHE | |
| SCHEMBL8431772 | 0.90 | CYP1B1 (0.91) | MAOBCYP1B1MAPTLMNABCHE | |
| SCHEMBL657311 | 0.90 | MAOB (0.81) | MAOBCYP1B1MAPTLMNABCHE |
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 82 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12576396-B2 | Polynorbornene/carbon black-cross-linked three-dimensional network-immobilized copper/gold (PNBI/CB-Cu/Au) nanocatalyst, and preparation method and use thereof | Hubei Engineering University (CN) | 2026-03-17 | — | — | US | claimed |
| US-20240261768-A1 | POLYNORBORNENE/CARBON BLACK-CROSS-LINKED THREE-DIMENSIONAL NETWORK-IMMOBILIZED COPPER/GOLD (PNBI/CB-Cu/Au) NANOCATALYST, AND PREPARATION METHOD AND USE THEREOF | Hubei Engineering University (CN) | 2024-08-08 | — | — | US | claimed |
| CN-117384199-A | Preparation of novel organic aluminum hydrogen compound and preparation method of unsaturated alcohol compound catalyzed by novel organic aluminum hydrogen compound | 北京理工大学 | 2024-01-12 | — | — | CN | claimed |
| CN-113620901-B | Crown ether derived chiral 1,1 '-bi-2, 2' -naphthol, preparation method and application thereof | 杭州师范大学 | 2023-02-10 | — | — | CN | claimed |
| CN-114797976-A | Preparation and application of crosslinked norbornene copolymer/carbon black three-dimensional network immobilized bimetallic copper/gold nano catalyst | 湖北工程学院 | 2022-07-29 | — | — | CN | claimed |
| CN-113620901-A | Crown ether derived chiral 1,1 '-bi-2, 2' -naphthol, preparation method and application thereof | 杭州师范大学 | 2021-11-09 | — | — | CN | claimed |
| US-12576396-B2 | Polynorbornene/carbon black-cross-linked three-dimensional network-immobilized copper/gold (PNBI/CB-Cu/Au) nanocatalyst, and preparation method and use thereof | Hubei Engineering University (CN) | 2026-03-17 | — | — | US | disclosed |
| US-20250051299-A1 | PRODUCTION METHOD FOR FLUOROMETHYL DERIVATIVE | DAIKIN INDUSTRIES, LTD. (JP) | 2025-02-13 | — | — | US | disclosed |
| US-12162854-B2 | Production method for fluoromethyl derivative | DAIKIN INDUSTRIES, LTD. (JP) | 2024-12-10 | — | — | US | disclosed |
| CN-116199597-B | Substituted phenyl diazonium salt and application thereof in catalytic preparation of 3-substituted indole compounds | 盐城利民农化有限公司 | 2024-12-03 | — | — | CN | disclosed |
| US-20240261768-A1 | POLYNORBORNENE/CARBON BLACK-CROSS-LINKED THREE-DIMENSIONAL NETWORK-IMMOBILIZED COPPER/GOLD (PNBI/CB-Cu/Au) NANOCATALYST, AND PREPARATION METHOD AND USE THEREOF | Hubei Engineering University (CN) | 2024-08-08 | — | — | US | disclosed |
| US-20240174698-A1 | MODULAR SYNTHESIS OF 1,2-AZABORINES VIA RING-OPENING BN-ISOSTERE BENZANNULATION | THE UNIVERSITY OF CHICAGO | 2024-05-30 | — | — | US | disclosed |
| CN-117843626-A | Ketone Kangxian-based triazole analogue, and preparation method and application thereof | 宿迁晨阳医药科技有限公司 | 2024-04-09 | — | — | CN | disclosed |
| WO-1992001675-A2 | SUBSTITUTED BICYCLIC BIS-ARYL COMPOUNDS EXHIBITING SELECTIVE LEUKOTRIENE B4 ANTAGONIST ACTIVITY, THEIR PREPARATION AND USE IN PHARMACEUTICAL COMPOSITIONS | RHONE-POULENC RORER S.A. (FR) | 1992-02-06 | — | — | WO | disclosed |
| US-4910303-A | Cataltyic reaction using N-alkylbis(2-hydroxyalkyl)amine | TEXACO CHEMICAL COMPANY (US) | 1990-03-20 | — | — | US | disclosed |
| US-4439418-A | UNSATURATED ARYL KETONE | HENKEL KGAA (DE) | 1984-03-27 | — | — | US | disclosed |
| EP-0004624-B1 | CHROMANON DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND THEIR USE AS MEDICINES AND GROWTH-PROMOTING AGENTS | BAYER AG (DE) | 1982-02-24 | — | — | EP | disclosed |
| US-4261988-A | ANTICHOLESTEROL AGENTS USED IN ANIMAL HUSBANDRY | BAYER AKTIENGESELLSCHAFT (DE) | 1981-04-14 | — | — | US | disclosed |
| EP-0004624-A2 | Chromanon derivatives, process for their preparation, and their use as medicines and growth-promoting agents | BAYER AG (DE) | 1979-10-17 | — | — | EP | disclosed |
| US-3989708-A | HYPOTENSIVE, CORONARY VESSEL DILATORS | BAYER AKTIENGESELLSCHAFT (DT) | 1976-11-02 | — | — | 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-20240261768-A1 | POLYNORBORNENE/CARBON BLACK-CROSS-LINKED THREE-DIMENSIONAL NETWORK-IMMOBILIZED COPPER/GOLD (PNBI/CB-Cu/Au) NANOCATALYST, AND PREPARATION METHOD AND USE THEREOF | AOC3, PNN, RPL23A | MAOB 382/4885CYP1B1 351/4885MAPT 1563/4885 |
| US-20240174698-A1 | MODULAR SYNTHESIS OF 1,2-AZABORINES VIA RING-OPENING BN-ISOSTERE BENZANNULATION | NBAS, DBF4, ALKBH2 | MAOB 96/4885CYP1B1 16/4885MAPT 4581/4885 |
| US-12576396-B2 | Polynorbornene/carbon black-cross-linked three-dimensional network-immobilized copper/gold (PNBI/CB-Cu/Au) nanocatalyst, and preparation method and use thereof | AOC3, PNN, SOD3 | MAOB 326/4885CYP1B1 229/4885MAPT 1217/4885 |
| US-12162854-B2 | Production method for fluoromethyl derivative | AFF1, AFF2, ROS1 | MAOB 20/4885CYP1B1 23/4885MAPT 3085/4885 |
| US-20250051299-A1 | PRODUCTION METHOD FOR FLUOROMETHYL DERIVATIVE | AFF1, AFF2, ROS1 | MAOB 20/4885CYP1B1 23/4885MAPT 3085/4885 |
“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.