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Bisandrographolide C

Bisandrographolide C

  • CAT Number: M131816
  • CAS Number: 160498-02-2
  • Molecular Formula: C40H56O8
  • Molecular Weight: 664.9
  • Purity: 98%
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<div style="orphans: 2; widows: 2;">
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">Bisandrographolide C (CAS&nbsp;160498-02-2)&nbsp;<span style="caret-color: rgb(0, 0, 0);">is a natural diterpenoid found in the herbs of Andrographis paniculata (Burm. f.) Nees.</span><span style="caret-color: rgb(0, 0, 0);">&nbsp;</span><span style="caret-color: rgb(0, 0, 0);">Andrographolide, a diterpenoid lactone, is one of the potent bioactive compounds isolated from&nbsp;</span><span style="caret-color: rgb(0, 0, 0);">Andrographis&nbsp;</span><span style="caret-color: rgb(0, 0, 0);">paniculata, shows </span><span style="caret-color: rgb(0, 0, 0);">bioactivities such as cytotoxicity, immunomodulation, hepatoprotectivity, apoptosis induction, and activates calcium‑permeable protein channel called transient receptor potential channels&nbsp;(TRPV4).</span></span></span></span></div>

Catalog Number M131816
CAS Number 160498-02-2
Molecular Formula

C40H56O8

Purity 98
Storage -20°C
IUPAC Name 4-[(E)-2-[(1R,4aS,5R,6R,8aR)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-[2-[(1R,4aS,5R,6R,8aR)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-(5-oxo-2H-furan-4-yl)ethyl]-2H-furan-5-one
InChI InChI=1S/C40H56O8/c1-23-7-11-31-37(3,16-13-33(43)39(31,5)21-41)28(23)10-9-25-19-30(48-35(25)45)27(26-15-18-47-36(26)46)20-29-24(2)8-12-32-38(29,4)17-14-34(44)40(32,6)22-42/h9-10,15,19,27-34,41-44H,1-2,7-8,11-14,16-18,20-22H2,3-6H3/b10-9+/t27?,28-,29-,30?,31+,32+,33-,34-,37+,38+,39+,40+/m1/s1
InChIKey WQHWOZANSOUSAY-LZBAHHAZSA-N
SMILES CC12CCC(C(C1CCC(=C)C2CC(C3C=C(C(=O)O3)C=CC4C(=C)CCC5C4(CCC(C5(C)CO)O)C)C6=CCOC6=O)(C)CO)O
Reference

<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Niranjan Reddy, V. L., et al. &quot;A new bis-andrographolide ether from Andrographis paniculata nees and evaluation of anti-HIV activity.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Natural Product Research</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;19.3 (2005): 223-230.<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Raghavan, Rahul, Sanith Cheriyamundath, and Joseph Madassery. &quot;Exploring the mechanisms of cytotoxic and anti-inflammatory property of andrographolide and its derivatives.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Pharmacognosy Reviews</i></span></span></span><span style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;"><span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">&nbsp;12.23 (2018).</span></span></span></span><br />
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