Cyanidin

Cyanidin

SCHEMBL608392

Cl.Oc1cc(O)c2cc(O)c(-c3ccc(O)c(O)c3)[o+]c2c1

nearest known ligand 0.97

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cyanidin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
DPP4 known ✓ P27487 3/20 0.94
EGFR known ✓ P00533 2/20 0.69
KDR known ✓ P35968 2/20 0.69
MAOA known ✓ P21397 1/20 0.54
CD38 P28907 11/20 0.97
F2 P00734 2/20 0.97
NR1H2 P55055 1/20 0.97
NR1H3 Q13133 1/20 0.97
GLO1 Q04760 5/20 0.94
SNCA P37840 3/20 0.94
OR51E2 Q9H255 2/20 0.73
EP300 Q09472 2/20 0.69
CREBBP Q92793 2/20 0.69
ALDH1A1 P00352 1/20 0.48
TSHR P16473 1/20 0.48
HSD17B10 Q99714 1/20 0.48
APP P05067 1/20 0.41
ALOX5 P09917 1/20 0.40

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
Cyanidin SCHEMBL1644900 1.00 CD38 (0.97) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL7931530 0.98 GLO1 (0.97) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL29414396 0.98 CD38 (1.00) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL20799 0.98 CD38 (1.00) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL156277 0.97 GLO1 (1.00) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL29547214 0.97 GLO1 (1.00) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL30423220 0.97 CD38 (0.97) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL29742342 0.97 CD38 (0.97) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL1945495 0.95 CD38 (0.88) CD38F2NR1H2NR1H3GLO1
Cyanidin SCHEMBL1230940 0.95 GLO1 (0.97) CD38F2NR1H2NR1H3GLO1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2479269-B1 PERILLA FRUTESCENS VAR. CRISPA-ORIGIN PROMOTER FUNCTIONING IN PETAL SUNTORY HOLDINGS LTD (JP) 2016-07-13 EP disclosed
US-8658779-B2 Perilla-derived promoter functioning in petals SUNTORY HOLDINGS LIMITED (JP) 2014-02-25 US disclosed
US-8410335-B2 Method for producing rose with altered petal colors SUNTORY HOLDINGS LIMITED (JP) 2013-04-02 US disclosed
EP-2479269-A1 PERILLA FRUTESCENS VAR. CRISPA-ORIGIN PROMOTER FUNCTIONING IN PETAL Suntory Holdings Limited (JP) 2012-07-25 EP disclosed
US-20120042421-A1 PERILLA-DERIVED PROMOTER FUNCTIONING IN PETALS SUNTORY HOLDINGS LIMITED (JP) 2012-02-16 US disclosed
EP-1652916-B1 PROCESS FOR PRODUCING ROSE WITH MODIFIED COLOR SUNTORY HOLDINGS LTD (JP) 2011-10-05 EP disclosed
US-20110126320-A1 Method for producing rose with altered petal colors SUNTORY HOLDINGS LIMITED (JP) 2011-05-26 US disclosed
EP-1652916-A1 PROCESS FOR PRODUCING ROSE WITH MODIFIED COLOR INTERNATIONAL FLOWER DEVELOPMENTS Proprietary Limited (AU) 2006-05-03 EP disclosed
EP-0929522-A1 INSECT-REPELLENT FORMULATIONS Pfizer Limited (GB) 1999-07-21 EP disclosed
EP-0901791-A1 Use of hawthorn fruits and/or leaves or blossom extract ROBUGEN GMBH PHARMAZEUTISCHE FABRIK (DE) 1999-03-17 EP disclosed
WO-1998013345-A1 INSECT-REPELLENT FORMULATIONS PFIZER LIMITED (GB) 1998-04-02 WO disclosed