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Verrucarin A
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Verrucarin A

CAS: 3148-09-2

Ref. 3D-FV171535

1mgTo inquire
Estimated delivery in United States, on Monday 26 Aug 2024

Product Information

Name:
Verrucarin A
Synonyms:
  • (10Z,12Z)-4-hydroxy-5,16a,21-trimethyl-4,5,6,7,16,16a,22,23-octahydro-3H,18H,19aH-spiro[16,18-methano[1,6,12]trioxacyclooctadecino[3,4-d]chromene-17,2'-oxirane]-3,9,14-trione
  • (4S,5R,10E,12Z,16R,16aS,17S,18R,19aR,23aR)-4,5,6,7,16,16a,19a,22-Octahydro-4-hydroxy-5,16a,21-trimethylspiro[16,18-methano-1H,3H,23H-[1,6,12]trioxacyclooctadecino[3,4-d][1]benzopyran-17(18H),2′-oxirane]-3,9,14-trione
  • (4S,5R,10E,12Z,16R,16aS,18R,19aR,23aR)-4-hydroxy-5,16a,21-trimethyl-4,5,6,7,16,16a,22,23-octahydro-3H,18H,19aH-spiro[16,18-methano[1,6,12]trioxacyclooctadecino[3,4-d]chromene-17,2'-oxirane]-3,9,14-trione
  • (4S,5R,10Z,12Z,16R,16aS,17R,18R,19aR,23aR)-4-hydroxy-5,16a,21-trimethyl-4,5,6,7,16,16a,22,23-octahydro-3H,18H,19aH-spiro[16,18-methano[1,6,12]trioxacyclooctadecino[3,4-d]chromene-17,2'-oxirane]-3,9,14-trione
  • 379Y
  • Ai3-29707
  • Antibiotic 379Y
  • Muconomycin
  • Muconomycin A
  • Nsc 126728
  • See more synonyms
  • Nsc 200736
  • Spiro(16,18-methano-1H,3H,23H-(1,6,12)trioxacyclooctadecino(3,4-d)(1)benzopyran-17(18H),2'-oxirane)-3,9,14-trione, 4,5,6,7,16,16a,19a,22-octahydro-4-hydroxy-5,16a,21-trimethyl-, stereoisomer
  • Spiro[16,18-methano-1H,3H,23H-[1,6,12]trioxacyclooctadecino[3,4-d][1]benzopyran-17(18H),2′-oxirane], verrucarin A deriv.
  • Spiro[16,18-methano-1H,3H,23H-[1,6,12]trioxacyclooctadecino[3,4-d][1]benzopyran-17(18H),2′-oxirane]-3,9,14-trione, 4,5,6,7,16,16a,19a,22-octahydro-4-hydroxy-5,16a,21-trimethyl-, (4S,5R,10E,12Z,16R,16aS,17S,18R,19aR,23aR)-
  • Ver A
  • Verrucarin A (8CI)(9CI)
  • Verrucarine A
Description:

Verrucarin A is a natural compound found in the etoac extract of the medicinal plant, Verruca carinata. Verrucarin A has been shown to exhibit anti-cancer properties in vitro and in vivo by inhibiting mitochondrial membrane potential, enzymatic inactivation, or polymerase chain reaction (PCR). This compound also has potent antimicrobial activity against opportunistic fungal infections. In addition, Verrucarin A has been shown to have cytotoxic effects on HL-60 cells and MDA-MB-231 breast cancer cells.
Verrucarin A binds to DNA and inhibits the transcription of target genes that are important for cell growth and proliferation. It is thought that this inhibition may be due to its ability to bind with DNA and block transcription factors from binding with their cognate sequences on DNA.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
488.53 g/mol
Formula:
C26H32O9
Purity:
Min. 95%
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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