SCHEMBL5059355

SCHEMBL5059355

FB(F)F.[BH4-].[Na+]

nearest known ligand 0.00

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
Lithium Ion SCHEMBL33523877 0.83
Fluoride Ion SCHEMBL29029426 0.83
SCHEMBL780 0.82
SCHEMBL29940263 0.82
SCHEMBL8778140 0.73
SCHEMBL1493171 0.73
Phosphine SCHEMBL63647 0.73
SCHEMBL20488766 0.73
SCHEMBL64817 0.73
Potassium SCHEMBL298979 0.73

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106278909-B Post-treatment method of mirabegron intermediate 浙江华海药业股份有限公司 2022-07-15 CN claimed
CN-114685515-A Preparation method of tofacitinib 上海蓝乐鸟实业有限公司 2022-07-01 CN claimed
CN-107827791-B A kind of synthetic method of stable isotope labeling Thiamphenicol 山东辉璟生物医药科技有限公司 2019-09-24 CN claimed
CN-106278909-A A kind of post-processing approach of Mirabegron intermediate 浙江华海药业股份有限公司 2017-01-04 CN claimed
CN-103664657-A New preparation method for bisoprolol fumarate UNIV SICHUAN 2014-03-26 CN claimed
CN-101573034-B Method for synthesizing (+) and (-) -1- (3, 4-dichlorophenyl) -3-azabicyclo [3.1.0] hexane DOV PHARMACEUTICAL INC 2013-01-02 CN claimed
CN-101573034-A Method for synthesizing (+) and (-) -1- (3, 4-dichlorophenyl) -3-azabicyclo [3.1.0] hexane DOV PHARMACEUTICAL INC (US) 2009-11-04 CN claimed
CN-117682975-A Preparation method of idexalone 重庆东得医药科技有限公司 2024-03-12 CN disclosed
CN-117586166-A Compound for preparing Ai Shali ketone and preparation method thereof 重庆东得医药科技有限公司 2024-02-23 CN disclosed
CN-108250046-B Synthesis method of resveratrol 上海巧坤化工科技有限公司 2023-09-15 CN disclosed
CN-106278909-B Post-treatment method of mirabegron intermediate 浙江华海药业股份有限公司 2022-07-15 CN disclosed
CN-114685515-A Preparation method of tofacitinib 上海蓝乐鸟实业有限公司 2022-07-01 CN disclosed
CN-111004135-B Synthesis method of (1R) -2- [ [ [2- (4-aminophenyl) ethyl ] amino ] methyl ] benzyl alcohol 苏州永健生物医药有限公司 2022-03-04 CN disclosed
CN-1143960-A Therapeutic heterocyclic compounds WELLCOME FOUND (GB) 1997-02-26 CN disclosed
CN-1006464-B PROCESS FOR PREPARING NAPHTHALENE DERIVATIVES TANABE SEIYAKU CO (JP) 1990-01-17 CN disclosed
CN-86100090-A The preparation method of naphthalene derivatives 1986-08-20 CN disclosed
US-4159966-A Chromatographic column packing THE DOW CHEMICAL COMPANY (US) 1979-07-03 US disclosed
US-4010280-A PHENOXYALKYLAMINE DERIVATIVES AND PREPARATION THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1977-03-01 US disclosed
US-4009275-A Phenoxypropylamine derivatives SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1977-02-22 US disclosed
US-3978140-A PROCESS FOR THE PREPARATION OF CARBINOLS ALDRICH-BORANES, INC. (US) 1976-08-31 US disclosed