Brucine

Brucine

SCHEMBL113229

COc1cc2c(cc1OC)[C@@]13CCN4CC5=CCO[C@H]6CC(=O)N2[C@H]1[C@H]6[C@H]5C[C@H]43

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ TAS2R10 Q9NYW0 2/20 1.00
▸ CHRM1 P11229 1/20 1.00
▸ SMN1; SMN2 Q16637 1/20 1.00
▸ GLRA1 P23415 14/20 0.73
▸ GLRB P48167 14/20 0.73
▸ CYP3A4 P08684 2/20 0.71
▸ MEN1 O00255 2/20 0.71
▸ KMT2A Q03164 2/20 0.71
▸ SCN1A P35498 1/20 0.71
▸ TAS2R46 P59540 1/20 0.71
▸ SCN2A Q99250 1/20 0.71
▸ SCN3A Q9NY46 1/20 0.71
▸ CYP1A2 P05177 1/20 0.67

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
Brucine SCHEMBL12293782 1.00 TAS2R10 (1.00) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL14029321 1.00 TAS2R10 (1.00) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL1648976 1.00 TAS2R10 (1.00) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL29391712 1.00 TAS2R10 (1.00) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL10307298 1.00 TAS2R10 (1.00) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL23468158 1.00 TAS2R10 (1.00) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL19476145 1.00 TAS2R10 (1.00) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL6233075 0.99 TAS2R10 (0.98) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL6794678 0.99 TAS2R10 (0.98) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB
Brucine SCHEMBL7253414 0.99 TAS2R10 (0.98) TAS2R10CHRM1SMN1; SMN2GLRA1GLRB

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

Appears in 10105 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122005546-A Application of brucine compounds in preparation of medicines for treating acute cerebral ischemic stroke 皖南医学院 2026-05-12 — — CN claimed
US-20260047566-A1 Durable and Edible Bait Roll Ups, Systems and Methods FLORIDA INSECT CONTROL GROUP LLC (US) 2026-02-19 — — US claimed
US-20260021089-A1 APPLICATION METHOD OF BRUCINE FOR TREATING AMYOTROPHIC LATERAL SCLEROSIS UNIV ZHEJIANG CHINESE MEDICAL (CN) 2026-01-22 — — US claimed
US-12446575-B1 Durable and edible bait roll ups, systems and methods FLORIDA INSECT CONTROL GROUP LLC (US) 2025-10-21 — — US claimed
US-20250302794-A1 COMPOSITIONS, METHODS AND SYSTEMS FOR THE TREATMENT OF CUTANEOUS DISORDERS VERRICA PHARMACEUTICALS INC. (US) 2025-10-02 — — US claimed
US-20250288538-A1 ABUSE AND MISUSE DETERRENT TRANSDERMAL SYSTEMS NUTRIBAND INC (US) 2025-09-18 — — US claimed
US-20250197666-A1 Battery Cell With Safety Layer DURACELL U.S. OPERATIONS, INC. 2025-06-19 — — US claimed
WO-2025128939-A1 BATTERY CELL WITH SAFETY LAYER DURACELL U.S. OPERATIONS, INC. (US) 2025-06-19 — — WO claimed
WO-2025120551-A1 INTERMEDIATE COMPOUND USED IN PREPARING HETEROCYCLE DERIVATIVE, METHOD FOR PREPARING SAME, AND METHOD FOR PREPARING HETEROCYCLE DERIVATIVE USING SAME 제이더블유중외제약 주식회사 2025-06-12 — — WO claimed
CN-120118006-A Sulfite compound with chirality and isomerism and application thereof 成都瀚巢生物技术研究有限公司 2025-06-10 — — CN claimed
US-4467102-A RACEMIC MODIFICATION WITH BRUCINE UBE INDUSTRIES, LTD. (JP) 1984-08-21 — — US claimed
US-4436823-A COLORIMETRIC ANALYSIS DRAGERWERK AKTIENGESELLSCHAFT (DE) 1984-03-13 — — US claimed
US-4424355-A Resolution of substituted dibenzo b,f!thiepin-3-carboxylic acid-5-oxides with brucine or ephedrine MERCK & CO., INC. (US) 1984-01-03 — — US claimed
EP-0084928-A1 Process for producing threo-3-(3,4-dihydroxyphenyl)serine SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1983-08-03 — — EP claimed
US-4250250-A Photographic process MITA INDUSTRIAL COMPANY LIMITED (JP) 1981-02-10 — — US claimed
US-4224457-A Process for manufacturing optically active sulfur-containing carboxylic acid SANTEN PHARMACEUTICAL CO., LTD. (JP) 1980-09-23 — — US claimed
US-RE29990-E Processes for stereospecifically preparing chiral 2-substituted-4-hydroxy-2-cyclopenten-1-one WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1979-05-08 — — US claimed
US-4151360-A Optically active amine salts HOFFMANN-LA ROCHE INC. (US) 1979-04-24 — — US claimed
US-4048224-A Process for resolving alanine, 3-fluoro and 2-deutero-3-fluoro-DL-alanine MERCK & CO., INC. (US) 1977-09-13 — — US claimed
US-3968141-A Processes for stereospecifically preparing chiral 2-substituted-4-hydroxy-2-cyclopenten-1-one WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1976-07-06 — — US claimed
Send feedback