CAS 21586-90-3

(1β,2α,11β,12α,15β)-13,20-époxy-1,2,11,12,14,15-hexahydroxypicras-3-en-16-one

Formule : C₂₀H₂₈O₉

InChI : InChI=1S/C20H28O9/c1-7-4-9(21)13(23)17(2)8(7)5-10-19-6-28-18(3,14(24)11(22)12(17)19)20(19,27)15(25)16(26)29-10/h4,8-15,21-25,27H,5-6H2,1-3H3/t8-,9-,10+,11+,12+,13+,14-,15-,17-,18+,19+,20+/m0/s1

Code InChI : InChIKey=ZBXITHPYBBXZRG-QYUWQHSUSA-N

SMILES : O[C@]12[C@@]34[C@@]([C@]5(C)[C@@](C[C@]3(OC(=O)[C@@H]1O)[H])(C(C)=C[C@H](O)[C@H]5O)[H])([C@@H](O)[C@H](O)[C@@]2(C)OC4)[H]

Synonymes :

• 5H-3,11cβ-(Epoxymethano)phenanthro[10,1-bc]pyran-5-one, 1,2,3,3a,4,6aβ,7,7aα,10,11,11a,11bα-dodecahydro-1β,2α,3aβ,4β,10α,11β-hexahydroxy-3α,8,11aβ-trimethyl-, (+)-
• Picras-3-en-16-one, 13,20-epoxy-1,2,11,12,14,15-hexahydroxy-, (1β,2α,11β,12α,15β)-
• Bruceine E
• (1β,2α,11β,12α,15β)-13,20-Epoxy-1,2,11,12,14,15-hexahydroxypicras-3-en-16-one
• WST 63

Bruceine E

CAS : 21586-90-3

Formule : C₂₀H₂₈O₉

Degré de pureté : 95%

Couleur et forme : Solid

Masse moléculaire : 412.4309

Ref: IN-DA00BHMS

Bruceine E

CAS : 21586-90-3

Bruceine E

Formule : C₂₀H₂₈O₉

Degré de pureté : ≥98%

Masse moléculaire : 412.43

Ref: 54-BUP07283

Bruceine E

CAS : 21586-90-3

Formule : C₂₀H₂₈O₉

Masse moléculaire : 412.44

Ref: 7W-GY3764

Bruceine E

CAS : 21586-90-3

Bruceine E is isolated from B. javanica seeds with hypoglycemia effects. Bruceine E can be used for studies about acting as an insulin secretagogue.

Formule : C₂₀H₂₈O₉

Degré de pureté : 99.88%

Couleur et forme : Solid

Masse moléculaire : 412.43

Ref: TM-TN1128

Bruceine E

CAS : 21586-90-3

Formule : C₂₀H₂₈O₉

Degré de pureté : 95%~99%

Masse moléculaire : 412.435

Ref: BP-BP4225

Bruceine E

CAS : 21586-90-3

Bruceine E is a quassinoid compound, which is derived from the seeds of the Brucea javanica plant. This compound belongs to the class of naturally occurring compounds known as quassinoids, which are primarily sourced from Simaroubaceae family plants. Bruceine E exhibits a mode of action that involves the inhibition of specific molecular targets, leading to disruption in cellular processes essential for cancer cell survival and proliferation. Its mechanism is characterized by interference with DNA synthesis and induction of apoptosis in specific tumor cells.

Formule : C₂₀H₂₈O₉

Degré de pureté : Min. 95%

Masse moléculaire : 412.44 g/mol

Ref: 3D-WAA58690