Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C28H38N2O4 |
Molecular Weight | 466.6123 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]4(C[C@H]1C[C@]2([H])N(CCC3=CC(OC)=C(OC)C=C23)C[C@@H]1CC)NCCC5=CC(O)=C(OC)C=C45
InChI
InChIKey=DTGZHCFJNDAHEN-OZEXIGSWSA-N
InChI=1S/C28H38N2O4/c1-5-17-16-30-9-7-19-13-27(33-3)28(34-4)15-22(19)24(30)11-20(17)10-23-21-14-26(32-2)25(31)12-18(21)6-8-29-23/h12-15,17,20,23-24,29,31H,5-11,16H2,1-4H3/t17-,20-,23+,24-/m0/s1
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL1875 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11913711 |
PubMed
Title | Date | PubMed |
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Evaluation of natural products as inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. | 1991 Jan-Feb |
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Metabolism of ipecac alkaloids cephaeline and emetine by human hepatic microsomal cytochrome P450s, and their inhibitory effects on P450 enzyme activities. | 2001 Jun |
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High-performance liquid chromatographic assay with fluorescence detection for the determination of cephaeline and emetine in human plasma and urine. | 2001 Jun 15 |
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The new beta-D-glucosidase in terpenoid-isoquinoline alkaloid biosynthesis in Psychotria ipecacuanha. | 2008 Dec 12 |
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Biochemistry and occurrence of o-demethylation in plant metabolism. | 2010 |
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Clonal diversity and conservation genetics of the medicinal plant Carapichea ipecacuanha (Rubiaceae). | 2010 Jan |
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Code System | Code | Type | Description | ||
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CEPHAELINE
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DTXSID50101652
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3533
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442195
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m3243
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QA971541A1
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100000174381
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483-17-0
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C005963
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207-591-6
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)