Biphenyl

Biphenyl

SCHEMBL3279732

OCc1ccccc1.c1ccc(-c2ccccc2)cc1

nearest known ligand 0.82

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.82
ALDH1A1 P00352 2/20 0.53
LTA4H P09960 1/20 0.52
TDP1 Q9NUW8 1/20 0.50
MKNK1 Q9BUB5 1/20 0.50
MKNK2 Q9HBH9 1/20 0.50
PRKCI P41743 1/20 0.50
HTT P42858 2/20 0.46
ABCC4 O15439 1/20 0.46
LMNA P02545 1/20 0.46
GAA P10253 1/20 0.46
PTGS1 P23219 1/20 0.46
TAAR1 Q96RJ0 1/20 0.46
BCL2L1 Q07817 2/20 0.46
MMP3 P08254 1/20 0.46
CALM1 P0DP23 1/20 0.45
BACE1 P56817 1/20 0.43
FFAR1 O14842 1/20 0.43
GRIN2B Q13224 1/20 0.42
RAB9A P51151 1/20 0.42

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.

Compoundsimilaritytop predictedshared targets
Biphenyl SCHEMBL27280595 0.92 TSHR (0.68) TSHRALDH1A1LTA4HMKNK1MKNK2
SCHEMBL70274 0.92 TSHR (0.68) TSHRALDH1A1LTA4HMKNK1MKNK2
SCHEMBL11274656 0.92 TSHR (0.68) TSHRALDH1A1LTA4HMKNK1MKNK2
Benzyl Alcohol SCHEMBL27703677 0.91 TSHR (1.00) TSHRALDH1A1LTA4HTDP1CALM1
Benzyl Alcohol SCHEMBL147 0.91
Benzyl Alcohol SCHEMBL27787318 0.91 TSHR (1.00) TSHRALDH1A1LTA4HTDP1CALM1
Benzyl Alcohol SCHEMBL11353823 0.91 TSHR (1.00) TSHRALDH1A1LTA4HTDP1CALM1
Benzyl Alcohol SCHEMBL9066990 0.91 TSHR (1.00) TSHRALDH1A1LTA4HTDP1CALM1
Benzyl Alcohol SCHEMBL433990 0.91 TSHR (1.00) TSHRALDH1A1LTA4HTDP1CALM1
Benzyl Alcohol SCHEMBL11680991 0.91 TSHR (1.00) TSHRALDH1A1LTA4HTDP1CALM1

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119751256-A Novel method for synthesizing bifenthrin 江苏优嘉植物保护有限公司 2025-04-04 CN claimed
CN-114252536-A High performance liquid chromatography method for determining related substances in bifonazole bulk drug 纳谱分析技术(苏州)有限公司 2022-03-29 CN claimed
CN-112179997-A Quality monitoring method for compound medicine containing bifonazole/chlorhexidine acetate 郑涛 2021-01-05 CN claimed
CN-1207286-C Synthesis procedure for biphenylimidazolyl-(1)-phenylmethane and related compounds MANUFACTURAS HUMBERTO BUKELE E (SV) 2005-06-22 CN claimed
CN-1429214-A Synthesis procedure for biphenylimidazolyl-(1)-phenylmethane and related compounds MANUFACTURAS HUMBERTO BUKELE E (SV) 2003-07-09 CN claimed
CN-119751256-A Novel method for synthesizing bifenthrin 江苏优嘉植物保护有限公司 2025-04-04 CN disclosed
CN-119751256-A Novel method for synthesizing bifenthrin 江苏优嘉植物保护有限公司 2025-04-04 CN disclosed
CN-114252536-B High performance liquid chromatography method for determining related substances in bulk drug of bifonazole 纳谱分析技术(苏州)有限公司 2024-08-27 CN disclosed
US-20240016151-A1 MICROCAPSULE AND LIQUID PESTICIDAL FORMULATION SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2024-01-18 US disclosed
CN-114252536-A High performance liquid chromatography method for determining related substances in bifonazole bulk drug 纳谱分析技术(苏州)有限公司 2022-03-29 CN disclosed
CN-112179997-A Quality monitoring method for compound medicine containing bifonazole/chlorhexidine acetate 郑涛 2021-01-05 CN disclosed
US-RE41254-E1 Synthesis procedure for biphenylimidazolyl-(1)-phenylmethane and related compounds MANUFACTURAS HUMBERTO TO BUELE HIJOS, S. (SV) 2010-04-20 US disclosed
US-6870057-B1 Reducing 4-phenylbenzophenone to alcohols, then condensing the intermediates with imidazole, to form bifonazole used as fungicides MANUFACTURAS HUMBERTO BUKELE E HIJOS, S.A. DE C.V. (SV) 2005-03-22 US disclosed
CN-1429214-A Synthesis procedure for biphenylimidazolyl-(1)-phenylmethane and related compounds MANUFACTURAS HUMBERTO BUKELE E (SV) 2003-07-09 CN disclosed
EP-1268494-A1 SULFUR SUBSTITUTED ARYLDIFLUOROMETHYLPHOSPHONIC ACIDS AS PTP-1B INHIBITORS Merck Frosst Canada & Co. (CA) 2003-01-02 EP disclosed
US-6498151-B2 PROTEIN TYROSINE PHOSPHATASES INHIBITORS, ESPECIALLY AS ANTIDIABETIC AGENTS MERCK FROSST CANADA & CO. (CA) 2002-12-24 US disclosed
US-20020091104-A1 Aryldifluoromethylphosphonic acids with sulfur-containing substituents as PTP-1B inhibitors MERCK FROSST CANADA LTD. (CA) 2002-07-11 US disclosed
WO-2001070753-A1 SULFUR SUBSTITUTED ARYLDIFLUOROMETHYLPHOSPHONIC ACIDS AS PTP-1B INHIBITORS MERCK FROSST CANADA & CO. (CA) 2001-09-27 WO disclosed
EP-1034245-A1 CONCENTRATED LIQUID CLEANER FOR HARD SURFACES Reckitt Benckiser Inc. (US) 2000-09-13 EP disclosed
WO-1999028428-A1 CONCENTRATED LIQUID CLEANER FOR HARD SURFACES RECKITT BENCKISER INC. (US) 1999-06-10 WO 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20020091104-A1 Aryldifluoromethylphosphonic acids with sulfur-containing substituents as PTP-1B inhibitors PTPRF, PTPRS, PTPRO TSHR 1867/4885ALDH1A1 312/4885LTA4H 1677/4885
US-20240016151-A1 MICROCAPSULE AND LIQUID PESTICIDAL FORMULATION ACHE, CAPG, MLEC TSHR 1380/4885ALDH1A1 4115/4885LTA4H 683/4885

“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.