Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C31H44O8 |
Molecular Weight | 544.6763 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 12 / 12 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]1(CC[C@@]2(C)C(CC[C@]3([H])[C@]2([H])CC[C@]4(C)[C@H](CC[C@]34O)C5=COC(=O)C=C5)=C1)O[C@@H]6O[C@@H](C)[C@H](OC)[C@@H](O)[C@H]6O
InChI
InChIKey=RKWPZPDLTYBKCL-RVZGXXANSA-N
InChI=1S/C31H44O8/c1-17-27(36-4)25(33)26(34)28(38-17)39-20-9-12-29(2)19(15-20)6-7-23-22(29)10-13-30(3)21(11-14-31(23,30)35)18-5-8-24(32)37-16-18/h5,8,15-17,20-23,25-28,33-35H,6-7,9-14H2,1-4H3/t17-,20-,21+,22-,23+,25-,26+,27-,28-,29-,30+,31-/m0/s1
Meproscillarin is a semisynthetic glycoside for the therapy of cardiac insufficiency. Meproscillarin is a drug with a high bioavailability (about 70%). Meproscillarin is at the only non-renal eliminated, lipophilic and short half-life digitalis and is therefore an ideal, cardiac inotropic agent for use in renal insufficiency. Meproscillarin can be used therapeutically in patients with liver cirrhosis, because a toxic accumulation is not to be expected. The rate of side effects of meproscillarin corresponded to that of other cardiac glycosides.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/348206
2-3 tablets of 0.25 mg daily
Route of Administration:
Oral
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C78322
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
251-493-6
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
100000081500
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
15942714
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
m9255
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | Merck Index | ||
|
1705
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
C87688
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
4012
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
DTXSID101031613
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
WYR1723LO7
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
C009079
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
SUB08758MIG
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
CHEMBL2106427
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY | |||
|
33396-37-1
Created by
admin on Fri Dec 15 16:47:24 GMT 2023 , Edited by admin on Fri Dec 15 16:47:24 GMT 2023
|
PRIMARY |
ACTIVE MOIETY