Chelerythrine

Chelerythrine

SCHEMBL9651282

COc1cc2ccc3c4c(OC)cc5c(c4c[n+](C)c3c2cc1OC)OCO5.COc1ccc2c(c[n+](C)c3c4cc5c(cc4ccc23)OCO5)c1OC.Cl

nearest known ligand 0.75

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 Chelerythrine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BCHE known ✓ P06276 5/20 0.75
ACHE known ✓ P22303 5/20 0.75
MAOA known ✓ P21397 1/20 0.75
PPARG known ✓ P37231 1/20 0.75
PRKCE known ✓ Q02156 1/20 0.74
CHRM1 known ✓ P11229 2/20 0.40
DRD2 known ✓ P14416 2/20 0.40
ADRA2B known ✓ P18089 2/20 0.40
ADRA2C known ✓ P18825 2/20 0.40
DRD1 known ✓ P21728 2/20 0.40
HTR2B known ✓ P41595 2/20 0.40
KCNH2 known ✓ Q12809 2/20 0.40
SIGMAR1 known ✓ Q99720 2/20 0.40
DPP4 known ✓ P27487 2/20 0.39
ALDH1A1 P00352 7/20 0.75
MAPT P10636 7/20 0.75
SMN1; SMN2 Q16637 7/20 0.75
HPGD P15428 5/20 0.75
MAPK1 P28482 5/20 0.75
KMT2A Q03164 5/20 0.75

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
Sanguinarium SCHEMBL9651303 0.92 BAD (0.70) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Hydrochloric Acid SCHEMBL9651229 0.89 ALDH1A1 (0.56) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Hydrochloric Acid SCHEMBL9651298 0.89 ALDH1A1 (0.65) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
SCHEMBL891378 0.89 TDP1 (0.65) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Hydrochloric Acid SCHEMBL891377 0.88 TDP1 (0.66) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Hydrochloric Acid SCHEMBL4261974 0.88 ALDH1A1 (0.57) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL4016265 0.88 ALDH1A1 (0.98) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL4980861 0.88 ALDH1A1 (0.98) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL288915 0.87 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL30527168 0.87 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5133981-A PURIFICATION OF BENZOPHENANTHRIDINE ALKALOIDS EXTRACTS FROM ALKALOID EXTRACTS ATRIX LABORATORIES, INC. (US) 1992-07-28 US claimed