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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H37NO4
Molecular Weight 403.5549
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EDIFOLONE

SMILES

[H][C@@]12CCC3(OCCO3)[C@@]1(C)CC[C@@]4([H])[C@@]2([H])CC=C5CC6(CC[C@]45CCN)OCCO6

InChI

InChIKey=HWXXPLRSBHPGSF-KNOXWWKRSA-N
InChI=1S/C24H37NO4/c1-21-6-4-20-18(19(21)5-7-24(21)28-14-15-29-24)3-2-17-16-23(26-12-13-27-23)9-8-22(17,20)10-11-25/h2,18-20H,3-16,25H2,1H3/t18-,19-,20-,21-,22+/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H37NO4
Molecular Weight 403.5549
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Edifolone (SC-35135) is a structurally unique class Ia antiarrhythmic agent. It acts as a sodium channel antagonist. Edifolone development has been discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed

Sample Use Guides

In Vitro Use Guide
SC-35135 was evaluated in guinea pig papillary muscle using standard microelectrode techniques to record transmembrane action potentials. SC-35135 markedly blocked Vmax (maximum rate of membrane depolarization) as a function of pacing frequency in the concentration range of 3 x 10(-6) to 3 x 10(-5) M, and was without effect on action potential duration. The effective refractory period was significantly shortened only at the highest concentration tested (3 x 10(-5) M). Rate constants for the onset of Vmax block determined at two stimulation rates, 60 and 200 pulses/min, were 0.17 +/- 0.052 and 0.06 +/- 0.005 (action potentials)-1, respectively, in the presence of 10(-5) M SC-35135. The recovery from Vmax depression following a train of stimuli was very slow in the presence of SC-35135. The average time constant for the recovery from block of Vmax after addition of 10(-5) M SC-35135 was 10.2 +/- 0.94 s. SC-35135 caused both a concentration- and stimulation frequency-dependent hyperpolarizing shift in the half point of the relationship between Vmax and resting membrane potential. Slow response (Ca current-dependent) action potentials were not changed by SC-35135 at concentrations less than or equal to 3 x 10(-5) M, indicating a lack of class IV antiarrhythmic activity.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:06:08 GMT 2023
Edited
by admin
on Fri Dec 15 16:06:08 GMT 2023
Record UNII
4XE0U1P5FJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EDIFOLONE
INN  
INN  
Official Name English
ESTR-5-ENE-3,17-DIONE, 10-(2-AMINOETHYL)-, CYCLIC BIS(1,2-ETHANEDIYL ACETAL)
Common Name English
10-(2-AMINOETHYL)ESTR-5-ENE-3,17-DIONE, CYCLIC BIS(ETHYLENE ACETAL)
Common Name English
edifolone [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
Code System Code Type Description
FDA UNII
4XE0U1P5FJ
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
PUBCHEM
68612
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
CAS
90733-40-7
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID40238249
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
NCI_THESAURUS
C75129
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
INN
6021
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
EVMPD
SUB06458MIG
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111177
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
SMS_ID
100000080511
Created by admin on Fri Dec 15 16:06:08 GMT 2023 , Edited by admin on Fri Dec 15 16:06:08 GMT 2023
PRIMARY
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