CANRENONE

Canrenone is an aldosterone antagonist that reduces sodium retention and supports heart failure management. Benefits include improved fluid balance. Side effects may include hyperkalemia, fatigue, and mild hypotension. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 667681af34fb Category: Tag:

Product Description


Mechanism of action

Canrenone is an active metabolite of spironolactone and a mineralocorticoid receptor antagonist. It inhibits aldosterone-mediated transcription of sodium-channel proteins in the distal nephron, reducing sodium retention and potassium loss. It also exhibits antifibrotic and mild antiandrogenic effects.

Benefits and advantages

Used in renal-electrolyte research, aldosterone-pathway investigations, heart-failure studies, RAAS-modelling, anti-fibrotic mechanism studies and endocrine-modulation research.

Side effects and risks

Risks include hyperkalaemia, endocrine effects (e.g., gynecomastia), hypotension and renal impairment. Handle as a steroidal mineralocorticoid antagonist.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C22H28O3

Molecular Weight

340.5 g/mol

CAS Number

976-71-6

Storage Condition

Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage.

Solubility

greater than or equal to 100 mg/mL at 70 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

CANRENONE; 976-71-6; Aldadiene; SC-9376; Canrenonum

IUPAC/Chemical Name

(8R,9S,10R,13S,14S,17R)-10,13-dimethylspiro[2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthrene-17,5'-oxolane]-2',3-dione

InChl Key

UJVLDDZCTMKXJK-WNHSNXHDSA-N

InChl Code

InChI=1S/C22H28O3/c1-20-9-5-15(23)13-14(20)3-4-16-17(20)6-10-21(2)18(16)7-11-22(21)12-8-19(24)25-22/h3-4,13,16-18H,5-12H2,1-2H3/t16-,17+,18+,20+,21+,22-/m1/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/13789;

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