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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H38N2O4.2ClH
Molecular Weight 539.534
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CEPHAELINE DIHYDROCHLORIDE

SMILES

Cl.Cl.[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=YAOHSWWVTZSRQM-JBKGYMEJSA-N
InChI=1S/C28H38N2O4.2ClH/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;2*1H/t17-,20-,23+,24-;;/m0../s1

HIDE SMILES / InChI

Molecular Formula C28H38N2O4
Molecular Weight 466.6123
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Evaluation of natural products as inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase.
1991 Jan-Feb
HIV-1 and HIV-2 reverse transcriptases: a comparative study of sensitivity to inhibition by selected natural products.
1992 May 29
Ipecacuanha: the South American vomiting root.
2008 Dec
Biochemistry and occurrence of o-demethylation in plant metabolism.
2010
Molecular phylogeography of Carapichea ipecacuanha, an amphitropical shrub that occurs in the understory of both semideciduous and evergreen forests.
2010 Apr
Clonal diversity and conservation genetics of the medicinal plant Carapichea ipecacuanha (Rubiaceae).
2010 Jan
Is a metabolic enzyme complex involved in the efficient and accurate control of Ipecac alkaloid biosynthesis in Psychotria ipecacuanha?
2010 Jul
Cell-based and cytokine-directed chemical screen to identify potential anti-multiple myeloma agents.
2010 Jul
Three new O-methyltransferases are sufficient for all O-methylation reactions of ipecac alkaloid biosynthesis in root culture of Psychotria ipecacuanha.
2010 Mar 5
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:55:16 GMT 2023
Edited
by admin
on Sat Dec 16 05:55:16 GMT 2023
Record UNII
5QL8Q0680S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CEPHAELINE DIHYDROCHLORIDE
Common Name English
EMETAN-6'-OL, 7',10,11-TRIMETHOXY-, DIHYDROCHLORIDE
Common Name English
CEPHAELINE HCL
Common Name English
7',10,11-TRIMETHOXYEMETAN-6'-OL DIHYDROCHLORIDE
Common Name English
6-ISOQUINOLINOL, 1-(((2S,3R,11BS)-3-ETHYL-1,3,4,6,7,11B-HEXAHYDRO-9,10-DIMETHOXY-2H-BENZO(A)QUINOLIZIN-2-YL)METHYL)-1,2,3,4-TETRAHYDRO-7-METHOXY-, HYDROCHLORIDE (1:2), (1R)-
Common Name English
(1R)-1-(((2S,3R,11BS)-3-ETHYL-1,3,4,6,7,11B-HEXAHYDRO-9,10-DIMETHOXY-2H-BENZO(A)QUINOLIZIN-2-YL)METHYL)-1,2,3,4-TETRAHYDRO-7-METHOXY-6-ISOQUINOLINOL DIHYDROCHLORIDE
Common Name English
DESMETHYLEMETINE DIHYDROCHLORIDE
Common Name English
CEPHAELINE, DIHYDROCHLORIDE
Common Name English
NSC-32944
Code English
(-)-CEPHAELINE DIHYDROCHLORIDE
Common Name English
CEPHALEINE HYDROCHLORIDE
Common Name English
Code System Code Type Description
PUBCHEM
23615629
Created by admin on Sat Dec 16 05:55:17 GMT 2023 , Edited by admin on Sat Dec 16 05:55:17 GMT 2023
PRIMARY
CAS
5853-29-2
Created by admin on Sat Dec 16 05:55:17 GMT 2023 , Edited by admin on Sat Dec 16 05:55:17 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-463-3
Created by admin on Sat Dec 16 05:55:17 GMT 2023 , Edited by admin on Sat Dec 16 05:55:17 GMT 2023
PRIMARY
NSC
32944
Created by admin on Sat Dec 16 05:55:17 GMT 2023 , Edited by admin on Sat Dec 16 05:55:17 GMT 2023
PRIMARY
FDA UNII
5QL8Q0680S
Created by admin on Sat Dec 16 05:55:17 GMT 2023 , Edited by admin on Sat Dec 16 05:55:17 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
Related Record Type Details
ACTIVE MOIETY