Chelerythrine

Chelerythrine

SCHEMBL4980861

COc1ccc2c(c[n+](C)c3c4cc5c(cc4ccc23)OCO5)c1OC.Cl

nearest known ligand 0.98

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 0.98
▸ ACHE known ✓ P22303 5/20 0.98
▸ MAOA known ✓ P21397 1/20 0.98
▸ PPARG known ✓ P37231 1/20 0.98
▸ PRKCE known ✓ Q02156 1/20 0.95
▸ CHRM1 known ✓ P11229 2/20 0.48
▸ DRD2 known ✓ P14416 2/20 0.48
▸ ADRA2B known ✓ P18089 2/20 0.48
▸ ADRA2C known ✓ P18825 2/20 0.48
▸ DRD1 known ✓ P21728 2/20 0.48
▸ HTR2B known ✓ P41595 2/20 0.48
▸ KCNH2 known ✓ Q12809 2/20 0.48
▸ SIGMAR1 known ✓ Q99720 2/20 0.48
▸ DPP4 known ✓ P27487 2/20 0.47
▸ ALDH1A1 P00352 7/20 0.98
▸ MAPT P10636 7/20 0.98
▸ SMN1; SMN2 Q16637 7/20 0.98
▸ HPGD P15428 5/20 0.98
▸ MAPK1 P28482 5/20 0.98
▸ KMT2A Q03164 5/20 0.98

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
Chelerythrine SCHEMBL4016265 1.00 ALDH1A1 (0.98) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL30527168 0.99 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL30527167 0.99 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL29357531 0.99 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL288915 0.99 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL3319851 0.98 ALDH1A1 (0.98) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL288916 0.98 ALDH1A1 (0.98) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL195109 0.98 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL30207103 0.98 ALDH1A1 (1.00) ALDH1A1MAPTSMN1; SMN2HPGDMAPK1
Chelerythrine SCHEMBL3973425 0.94 ALDH1A1 (0.91) 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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117064890-A Application of chelerythrine hydrochloride in preparing medicament for treating psoriasis 贵州省天然产物研究中心 2023-11-17 — — CN claimed
CN-110679612-A Agricultural insecticidal composition for preventing and treating corn borers 宁波市鄞州赛弗兑食品科技有限公司 2020-01-14 — — CN claimed
CN-101775022-A Ion-pair compound of chelerythrine from Chinese medicine extracts, preparation and application thereof JIANGUO ZENG 2010-07-14 — — CN claimed
CN-118638126-A Tritiated sanguinarine and preparation method and application thereof 湖南农业大学 2024-09-13 — — CN disclosed
CN-117121918-A Application of sanguinarine and analogues thereof 贵州大学 2023-11-28 — — CN disclosed
CN-117064890-A Application of chelerythrine hydrochloride in preparing medicament for treating psoriasis 贵州省天然产物研究中心 2023-11-17 — — CN disclosed
CN-117064890-A Application of chelerythrine hydrochloride in preparing medicament for treating psoriasis 贵州省天然产物研究中心 2023-11-17 — — CN disclosed
CN-117064890-A Application of chelerythrine hydrochloride in preparing medicament for treating psoriasis 贵州省天然产物研究中心 2023-11-17 — — CN disclosed
CN-114456144-B Intermediate compound for preparing sanguinarine by chemical synthesis and preparation method thereof 宁波九胜创新医药科技有限公司 2023-10-13 — — CN disclosed
CN-114456185-B Chemical synthesis method of sanguinarine 宁波九胜创新医药科技有限公司 2023-09-01 — — CN disclosed
CN-113816967-B Method, composition and application of bio-orthogonal photocatalytic oxidative dehydrogenation activated antitumor compound 华南理工大学 2023-04-21 — — CN disclosed
CN-101824061-B Baicalin ion pair medicine from traditional Chinese medicine of baikal skullcap root as well as preparation method and application thereof ZENG JIANGUO (CN) 2012-02-15 — — CN disclosed
CN-101195627-B New application of benzo [C] phenanthridine and protopine in producing overriding resistant bacterium medicament KUNMING GENERAL HOSPITAL CHENGDU MILITARY AREA 2010-11-24 — — CN disclosed
CN-101824061-A Baicalin ion pair medicine from traditional Chinese medicine of baikal skullcap root as well as preparation method and application thereof JIANGUO ZENG 2010-09-08 — — CN disclosed
CN-101775022-A Ion-pair compound of chelerythrine from Chinese medicine extracts, preparation and application thereof JIANGUO ZENG 2010-07-14 — — CN disclosed
CN-101195627-A New application of benzo [C] phenanthridine and protopine in producing overriding resistant bacterium medicament KUNMING GENERAL HOSPITAL CHENG (CN) 2008-06-11 — — CN disclosed
CN-100387602-C Chelerythrine compound and its preparing method QINGHONG ZHANG (CN) 2008-05-14 — — CN disclosed
US-20080076781-A1 PSEUDOBASE BENZO[C]PHENANTHRIDINES WITH IMPROVED EFFICACY, STABILITY, AND SAFETY MARINUS PHARMACEUTICALS INC. (US) 2008-03-27 — — US disclosed
CN-1891703-A Chelerythrine compound and its preparing method ZHANG QINGHONG (CN) 2007-01-10 — — CN disclosed
CN-1532197-A Process for separating and preparing hig purity samguinarine and chelerythrine 湖南师范大学 2004-09-29 — — CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080076781-A1 PSEUDOBASE BENZO[C]PHENANTHRIDINES WITH IMPROVED EFFICACY, STABILITY, AND SAFETY TOP1, TOP2B, TOP2A BCHE 1477/4885ACHE 2721/4885MAOA 2631/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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