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Contents

   



(Top)
  


1 Structure  




2 Extraction  




3 Pharmacological activity  




4 See also  




5 References  













Caldoramide







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From Wikipedia, the free encyclopedia
  

Caldoramide
Identifiers

CAS Number

3D model (JSmol)

PubChem CID
UNII

  • InChI=1S/C37H59N5O6/c1-22(2)19-28(35(45)42-27(29(48-13)21-30(42)43)20-26-17-15-14-16-18-26)40(11)37(47)33(25(7)8)41(12)36(46)31(23(3)4)38-34(44)32(24(5)6)39(9)10/h14-18,21-25,27-28,31-33H,19-20H2,1-13H3,(H,38,44)/t27-,28-,31-,32-,33-/m0/s1

    Key: XMIMMOXGNBQXIJ-VLQZMBLPSA-N

  • CC(C)CC(C(=O)N1C(C(=CC1=O)OC)CC2=CC=CC=C2)N(C)C(=O)C(C(C)C)N(C)C(=O)C(C(C)C)NC(=O)C(C(C)C)N(C)C

Properties

Chemical formula

 C37H59N5O6
Molar mass 669.908 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Caldoramide is a pentapeptide[1] isolated from the cyanobacteria Caldora penicillata.[2] It has cytotoxic effects on cancer cells and has been the subject of extensive oncological research.[3] It is structurally analogous to belamide A and dolastatin 15. Its appearance is that of a powdery, white, substance.[3]

Structure[edit]

The N-terminus for Caldoramide is N,N-dimethylvaline which is attached to a valine which is attached to an N-Me-valine connected to an N-Me-isoleucine which is attached to the C-terminus. The molecule can also be written as N,N-diMe-Val-Val-N-Me-Val-N-Me-Ile-3-O-Me-4-benzylpyrrolinone.[3]

Extraction[edit]

Freeze-dried samples of Caldora penicillata had EtOAc−MeOH and H2O−EtOH applied to them in order to extract Caldoramide. The extracts were partitioned with n-BuOH and H2O and then fractions were taken based on solubility in either EtOAc or BuOH. Caldoramide was extracted from the BuOH soluble fraction.[3]

Pharmacological activity[edit]

Caldoramide has been found to be cytotoxic against HCT116 colorectal cancer cell lines.[3]

See also[edit]

References[edit]

  1. ^ Wunder A, Rothemund M, Schobert R (2018). "Synthesis and anticancer activity of the proposed structure of caldoramide, an N-peptidyltetramate from the cyanobacterium Caldora penicillata". Tetrahedron. 74 (38): 5138–5142. doi:10.1016/j.tet.2018.04.004. S2CID 103025376.
  • ^ Iwasaki A, Tadenuma T, Sumimoto S, Shiota I, Matsubara T, Saito-Nakano Y, et al. (November 2018). "Hoshinoamides A and B, Acyclic Lipopeptides from the Marine Cyanobacterium Caldora penicillata". Journal of Natural Products. 81 (11): 2545–2552. doi:10.1021/acs.jnatprod.8b00643. PMID 30387355. S2CID 53725718.
  • ^ a b c d e Gunasekera SP, Imperial L, Garst C, Ratnayake R, Dang LH, Paul VJ, Luesch H (July 2016). "Caldoramide, a Modified Pentapeptide from the Marine Cyanobacterium Caldora penicillata". Journal of Natural Products. 79 (7): 1867–71. doi:10.1021/acs.jnatprod.6b00203. PMC 5215049. PMID 27380142.
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