U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H39NO6
Molecular Weight 449.5803
Optical Activity UNSPECIFIED
Defined Stereocenters 12 / 12
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Condelphine

SMILES

CCN1C[C@]2(COC)CC[C@H](O)[C@@]34[C@@H]5C[C@H]6[C@H](OC(C)=O)[C@@H]5[C@](O)(C[C@@H]6OC)[C@@H](C[C@H]23)[C@@H]14

InChI

InChIKey=ZEBMMHUDQRRILP-YNLINXDKSA-N
InChI=1S/C25H39NO6/c1-5-26-11-23(12-30-3)7-6-19(28)25-15-8-14-17(31-4)10-24(29,16(22(25)26)9-18(23)25)20(15)21(14)32-13(2)27/h14-22,28-29H,5-12H2,1-4H3/t14-,15-,16+,17+,18-,19+,20-,21+,22-,23+,24+,25-/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.6 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Antagonist pharmacology of desensitizing and non-desensitizing nicotinic acetylcholine receptors in cockroach neurons.
2016-09
Antifungal diterpenoid alkaloids from Delphinium denudatum.
1997-05
The structures of condelphine, isotalatizidine, and talatizidine.
1967-08-02
Name Type Language
CODELPHINE
Preferred Name English
Condelphine
Common Name English
Aconitane-1,8,14-triol, 20-ethyl-16-methoxy-4-(methoxymethyl)-, 14-acetate, (1?,14?,16?)-
Systematic Name English
Kondelfin
Common Name English
(3S,6S,7R,7aR,8S,9R,10S,11aS,14R)-1-ethyl-6,11a-dihydroxy-10-methoxy-3-(methoxymethyl)tetradecahydro-1H-3,6a,12-(epiethane[1,1,2]triyl)-7,9-methanonaphtho[2,3-b]azocin-8-yl acetate
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
231-562-7
Created by admin on Mon Mar 31 22:19:50 GMT 2025 , Edited by admin on Mon Mar 31 22:19:50 GMT 2025
PRIMARY
PUBCHEM
441720
Created by admin on Mon Mar 31 22:19:50 GMT 2025 , Edited by admin on Mon Mar 31 22:19:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID50997693
Created by admin on Mon Mar 31 22:19:50 GMT 2025 , Edited by admin on Mon Mar 31 22:19:50 GMT 2025
PRIMARY
FDA UNII
E55EVL23BY
Created by admin on Mon Mar 31 22:19:50 GMT 2025 , Edited by admin on Mon Mar 31 22:19:50 GMT 2025
PRIMARY
CAS
7633-69-4
Created by admin on Mon Mar 31 22:19:50 GMT 2025 , Edited by admin on Mon Mar 31 22:19:50 GMT 2025
PRIMARY