Cyanidin

Cyanidin

SCHEMBL7931530

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

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 0.97
EGFR known ✓ P00533 2/20 0.69
KDR known ✓ P35968 2/20 0.69
MAOA known ✓ P21397 1/20 0.56
GLO1 Q04760 5/20 0.97
SNCA P37840 3/20 0.97
CD38 P28907 11/20 0.94
F2 P00734 2/20 0.94
NR1H2 P55055 1/20 0.94
NR1H3 Q13133 1/20 0.94
OR51E2 Q9H255 2/20 0.74
EP300 Q09472 2/20 0.69
CREBBP Q92793 2/20 0.69
ALDH1A1 P00352 1/20 0.47
TSHR P16473 1/20 0.47
HSD17B10 Q99714 1/20 0.47
APP P05067 1/20 0.39
ALOX5 P09917 1/20 0.39

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 0.98 CD38 (0.97) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL29547214 0.98 GLO1 (1.00) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL156277 0.98 GLO1 (1.00) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL608392 0.98 CD38 (0.97) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL1230940 0.97 GLO1 (0.97) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL29414396 0.97 CD38 (1.00) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL20799 0.97 CD38 (1.00) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL29742342 0.95 CD38 (0.97) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL30423220 0.95 CD38 (0.97) GLO1SNCADPP4CD38F2
Cyanidin SCHEMBL1945495 0.94 CD38 (0.88) GLO1SNCADPP4CD38F2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6235162-B1 FRACTIONAL DISTILLATION, FLASHOVER DISTILLATION SACHEM, INC. 2001-05-22 US disclosed
US-5904823-A Methods of purifying hydroxylamine solutions and converting hydroxylamine salts to hydroxylamine SACHEM, INC. (US) 1999-05-18 US disclosed
US-5843318-A Methods of purifying hydroxlamine solutions and separating hydroxylamine from hydroxlamine salts SACHEM, INC. (US) 1998-12-01 US disclosed
EP-0870532-A2 Methods of purifying hydroxylamine solutions and converting hydroxylamine salts to hydroxylamine Sachem, Inc. (US) 1998-10-14 EP disclosed
EP-0149153-B1 PROCESS FOR PRODUCING AQUEOUS HYDROXYLAMINE SOLUTIONS BASF Aktiengesellschaft (DE) 1988-06-01 EP disclosed
EP-0149154-B1 PROCESS FOR PRODUCING AQUEOUS HYDROXYLAMMONIUM CARBONATE SOLUTIONS BASF Aktiengesellschaft (DE) 1987-08-12 EP disclosed
US-4645579-A Preparation of aqueous hydroxylamine solutions BASF AKTIENGSELLSCHAFT (DE) 1987-02-24 US disclosed
US-4601800-A Preparation of aqueous solutions of hydroxylammonium carbonate BASF AKTIENGESELLSCHAFT (DE) 1986-07-22 US disclosed
EP-0149154-A2 Process for producing aqueous hydroxylammonium carbonate solutions BASF Aktiengesellschaft (DE) 1985-07-24 EP disclosed
EP-0149153-A2 Process for producing aqueous hydroxylamine solutions BASF Aktiengesellschaft (DE) 1985-07-24 EP disclosed