Piconol

Piconol

SCHEMBL2647157

O.OCc1ccccn1

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Piconol. 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
Piconol SCHEMBL31122945 1.00 — —
Piconol SCHEMBL29530498 0.97 — —
Piconol SCHEMBL29266 0.97 — —
Piconol SCHEMBL2909774 0.95 HRH1 (0.48) —
Piconol SCHEMBL28642302 0.95 HRH1 (0.52) —
Piconol SCHEMBL15050907 0.95 — —
Piconol SCHEMBL7153449 0.95 — —
Piconol SCHEMBL7153451 0.95 — —
Piconol SCHEMBL3074525 0.95 — —
Piconol SCHEMBL19874569 0.95 — —

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111910256-A Single crystal preparation method of caffeine impurity II 山东新华制药股份有限公司 2020-11-10 — — CN claimed
CN-111910256-A Single crystal preparation method of caffeine impurity II 山东新华制药股份有限公司 2020-11-10 — — CN disclosed
EP-2221311-B1 Novel nucleic acid base pair TAGCYX BIOTECHNOLOGIES (JP) 2013-08-21 — — EP disclosed
EP-1114827-B1 NOVEL NUCLEIC ACID BASE PAIR JAPAN SCIENCE & TECH AGENCY (JP) 2010-11-17 — — EP disclosed
EP-2223931-A1 Novel nucleic acid base pair Japan Science and Technology Agency (JP) 2010-09-01 — — EP disclosed
EP-2221311-A1 Novel nucleic acid base pair Japan Science and Technology Agency (JP) 2010-08-25 — — EP disclosed
US-7667031-B2 Nucleic acid base pair JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2010-02-23 — — US disclosed
US-20090286247-A1 Novel nucleic acid base pair JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2009-11-19 — — US disclosed
US-7101992-B1 Nucleic acid base pair JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2006-09-05 — — US disclosed
US-20050191689-A1 Novel nucleic acid base pair HIRAO, ICHIRO (JP) 2005-09-01 — — US disclosed
EP-1114827-A1 NOVEL NUCLEIC ACID BASE PAIR Japan Science and Technology Corporation (JP) 2001-07-11 — — EP disclosed
EP-0915875-A2 SUBSTITUTED TRIAZOLO-PYRIDAZINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS MERCK SHARP &amp; DOHME LTD. (GB) 1999-05-19 — — EP disclosed
WO-1998004559-A2 SUBSTITUTED TRIAZOLO-PYRIDAZINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS MERCK SHARP & DOHME LIMITED (GB) 1998-02-05 — — WO disclosed
US-5166078-A HAPTEN-MACROMOLECULE CONJUGATES USEFUL IN HAPTEN ASSAYS IDEXX LABORATORIES, INC. (US) 1992-11-24 — — US disclosed
EP-0256551-A2 Hapten-macromolecule conjugates useful in hapten assays AGRITECH SYSTEMS, Inc. (US) 1988-02-24 — — EP disclosed
US-4656036-A Antibiotics Tejeramycin and production thereof MERCK & CO., INC. (US) 1987-04-07 — — US disclosed
US-4482708-A VIRICIDES; POTENTIATION AND INDUCTION OF INTERFERON PRODUCTION NGUYEN NICOLAS C 1984-11-13 — — US disclosed
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