Known targets — ChEMBL curated mechanism
ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4
The experimentally established mechanism targets of Biphenyl. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SLC6A4 known ✓ | P31645 | 1/20 | 0.50 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.90 |
| ▸ | MAPK1 | P28482 | 2/20 | 0.56 |
| ▸ | TAAR1 | Q96RJ0 | 2/20 | 0.56 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.56 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.56 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.56 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.56 |
| ▸ | NOTUM | Q6P988 | 1/20 | 0.56 |
| ▸ | MMP3 | P08254 | 1/20 | 0.56 |
| ▸ | BCL2L1 | Q07817 | 1/20 | 0.56 |
| ▸ | NPC1 | O15118 | 2/20 | 0.50 |
| ▸ | RAB9A | P51151 | 2/20 | 0.50 |
| ▸ | ATM | Q13315 | 1/20 | 0.50 |
| ▸ | SLC22A2 | O15244 | 1/20 | 0.50 |
| ▸ | SLC22A1 | O15245 | 1/20 | 0.50 |
| ▸ | SLC22A3 | O75751 | 1/20 | 0.50 |
| ▸ | MAOA | P21397 | 1/20 | 0.47 |
| ▸ | NFKB1 | P19838 | 1/20 | 0.47 |
| ▸ | NFKB2 | Q00653 | 1/20 | 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 | |
|---|---|---|---|---|
| Biphenyl SCHEMBL28147228 | 1.00 | ALDH1A1 (0.90) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL29792028 | 1.00 | ALDH1A1 (0.90) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL27949297 | 0.95 | ALDH1A1 (0.82) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL10806270 | 0.95 | ALDH1A1 (0.82) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL28142950 | 0.95 | ALDH1A1 (0.82) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL11524760 | 0.95 | ALDH1A1 (0.82) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL1150073 | 0.95 | ALDH1A1 (0.82) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL11584967 | 0.95 | ALDH1A1 (0.82) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL3857670 | 0.95 | ALDH1A1 (0.82) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 | |
| Biphenyl SCHEMBL1358618 | 0.95 | ALDH1A1 (1.00) | ALDH1A1MAPK1TAAR1CYP1A2CYP3A4 |
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 183 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-11572473-B2 | Biorenewable hydrocarbon compositions and their uses | KRATON POLYMERS LLC (US) | 2023-02-07 | — | — | US | claimed |
| CN-214693951-U | Bromination reaction system for production of cyanoborobiphenyl | 江苏新瑞药业有限公司 | 2021-11-12 | — | — | CN | claimed |
| US-20210189132-A1 | Biorenewable Hydrocarbon Compositions and Their Uses | KRATON POLYMERS LLC (US) | 2021-06-24 | — | — | US | claimed |
| EP-3838998-A1 | BIORENEWABLE HYDROCARBON COMPOSITIONS AND THEIR USES | Kraton Polymers Research B.V. (NL) | 2021-06-23 | — | — | EP | claimed |
| WO-2020248717-A1 | DIAPHRAGM FOR SOUND GENERATING DEVICE AND SOUND GENERATING DEVICE | 歌尔股份有限公司 | 2020-12-17 | — | — | WO | claimed |
| CN-105198863-B | Method for preparing high-purity losartan | 浙江华海药业股份有限公司 | 2020-10-02 | — | — | CN | claimed |
| CN-106117146-A | A kind of method preparing irbesartan condensation substance | 浙江华海药业股份有限公司 | 2016-11-16 | — | — | CN | claimed |
| CN-106083826-A | A kind of irbesartan isomer and the preparation method of intermediate thereof | 浙江华海药业股份有限公司 | 2016-11-09 | — | — | CN | claimed |
| JP-62187434-A | — | — | None | — | — | JP | disclosed |
| CN-122055371-A | Faster automated iterative C-C bond formation | 伊利诺伊大学评议会 | 2026-05-15 | — | — | CN | disclosed |
| EP-3916035-B1 | METHOD FOR CONTROLLING CROSS-LINKING REACTION RATE AND OF A CROSS-LINKING COMPOUND | Delsper LP (US) | 2025-05-21 | — | — | EP | disclosed |
| WO-2025042679-A1 | FASTER AUTOMATED ITERATIVE C-C BOND FORMATION | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) | 2025-02-27 | — | — | WO | disclosed |
| CN-114068847-B | Composition for organic photoelectric device, organic photoelectric device and display device | 三星SDI株式会社 | 2024-12-13 | — | — | CN | disclosed |
| CN-114761477-B | Flame-retardant polyester molding compositions | 巴斯夫欧洲公司 | 2024-05-24 | — | — | CN | disclosed |
| US-4876251-A | ANTIBIOTICS | TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) | 1989-10-24 | — | — | US | disclosed |
| EP-0249909-A1 | Tricyclic penam compounds, their production and their use | Takeda Chemical Industries, Ltd. (JP) | 1987-12-23 | — | — | EP | disclosed |
| JP-S62187434-A | PRODUCTION OF DIPHENYLCARBOXYLIC ACID ESTER | ASAHI CHEM IND CO LTD | 1987-08-15 | — | — | JP | disclosed |
| US-4560447-A | Electrolytic process for preparation of α-alkylated acetic acid derivatives | OTSUKA KAGAKU KABUSHIKI KAISHA (JP) | 1985-12-24 | — | — | US | disclosed |
| US-4554360-A | DIARYLIODONIUM SALT, IODOARENE, COUPLING | NIPPON PETROCHEMICALS COMPANY, LIMITED (JP) | 1985-11-19 | — | — | US | disclosed |
| US-4251655-A | GASTRIC ACID ANTISECRETORY AGENTS | MCNEILAB, INC. (US) | 1981-02-17 | — | — | US | disclosed |