Biphenyl

Biphenyl

SCHEMBL1502248

C1CCC(C2CCCCC2)CC1.P

nearest known ligand 0.80

Full drug profile on Sugi Atlas →

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.80
HSD17B10 Q99714 1/20 0.38
SLC18A3 Q16572 1/20 0.38
THRB P10828 1/20 0.33
CES2 O00748 1/20 0.33
CES1 P23141 1/20 0.33
HSD11B1 P28845 1/20 0.33
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
TSHR P16473 1/20 0.33
MAPT P10636 1/20 0.32
NOS1 P29475 1/20 0.32
NOS2 P35228 1/20 0.32
EPHX1 P07099 1/20 0.32
HIF1A Q16665 1/20 0.32

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
Phosphine SCHEMBL9452572 1.00 ALDH1A1 (0.80) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL7738712 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL22284066 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL231054 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
Biphenyl SCHEMBL2997707 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL241806 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL7741464 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL22284064 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL2999797 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2
SCHEMBL48866 0.95 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBCES2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117486934-A Preparation method of chemiluminescent agent and chemiluminescent agent 苏州亚科科技股份有限公司 2024-02-02 CN claimed
US-10411301-B2 Ionic liquids and preparation method thereof MICROVAST POWER SYSTEMS CO., LTD. (CN) 2019-09-10 US claimed
CN-109020979-A A kind of electroluminescent organic material and preparation method and application with heterocycle structure 中节能万润股份有限公司 2018-12-18 CN claimed
US-20170222266-A1 IONIC LIQUIDS AND PREPARATION METHOD THEREOF MICROVAST POWER SYSTEMS CO., LTD. (CN) 2017-08-03 US claimed
US-9365596-B2 Method for preparing quaternary phosphonium salts MICROVAST POWER SYSTEMS CO., LTD. (CN) 2016-06-14 US claimed
US-20150166587-A1 METHOD FOR PREPARING QUATERNARY PHOSPHONIUM SALTS MICROVAST POWER SYSTEMS CO., LTD. (CN) 2015-06-18 US claimed
EP-1070075-B1 CHIRAL PHOSPHORATED LIGANDS USEFUL IN CATALYSTS CHEMI SPA (IT) 2003-10-08 EP claimed
EP-1070075-A1 CHIRAL PHOSPHORATED LIGANDS USEFUL IN CATALYSTS CHEMI S.p.A. (IT) 2001-01-24 EP claimed
WO-1999052915-A1 CHIRAL PHOSPHORATED LIGANDS USEFUL IN CATALYSTS CHEMI S.P.A. (IT) 1999-10-21 WO claimed
EP-0333489-B1 Process for the removal of heavy metal ions from phosphoric acid IMI TAMI INSTITUTE RESEARCH (IL) 1994-06-22 EP claimed
EP-4701782-A1 CATALYST SYSTEM AND ETHYLENE OLIGOMERIZATION PROCESS FOR THE PREPARATION OF LINEAR ALPHA OLEFINS Chevron Phillips Chemical Company LP (US) 2026-03-04 EP disclosed
EP-4701783-A1 PHOSPHINE-IMINO-QUINOLINE AND RELATED LIGANDS FOR USE IN ETHYLENE OLIGOMERIZATION PROCESSES Chevron Phillips Chemical Company LP (US) 2026-03-04 EP disclosed
EP-3609891-B1 SUBSTITUTED HETEROCYCLE FUSED GAMMA-CARBOLINES SYNTHESIS INTRA CELLULAR THERAPIES INC (US) 2026-02-11 EP disclosed
CN-117355373-B Ethylene oligomerization process 切弗朗菲利浦化学公司 2025-05-16 CN disclosed
CN-119528662-A Preparation method of trans-S-alkenyl thio pyridazine compound 常州大学 2025-02-28 CN disclosed
US-4081491-A HEAT CURABLE SHELL OIL COMPANY (US) 1978-03-28 US disclosed
US-4061681-A Method for the preparation of mono- or poly [dialkyl or dicycloalkylphosphonylmethyl] aromatic carbocyclic compounds AMERICAN CYANAMID COMPANY (US) 1977-12-06 US disclosed
US-3988152-A Epoxy resin photoresist with iodoform and bismuth triphenyl AMERICAN CAN COMPANY (US) 1976-10-26 US disclosed
US-3977874-A CATIONIC CATALYST, PHOTOPOLYMERIZATION AMERICAN CAN COMPANY (US) 1976-08-31 US disclosed
US-3977878-A Epoxy resin photoresist with iodoform and bismuth triphenyl AMERICAN CAN COMPANY (US) 1976-08-31 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 (3 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-20170222266-A1 IONIC LIQUIDS AND PREPARATION METHOD THEREOF DNMT3A, SOD1, CLK2 ALDH1A1 3407/4885HSD17B10 4199/4885SLC18A3 882/4885
US-10411301-B2 Ionic liquids and preparation method thereof DNMT3A, SOD1, CLK2 ALDH1A1 3407/4885HSD17B10 4199/4885SLC18A3 882/4885
US-20150166587-A1 METHOD FOR PREPARING QUATERNARY PHOSPHONIUM SALTS PHPT1, PHOSPHO1, PTEN ALDH1A1 4827/4885HSD17B10 2780/4885SLC18A3 3806/4885

“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.