Muironolide A

Muironolide A
Names
	IUPAC name (1S,2E,4R,7R,11S,14E,16R,17R)-11-[(1S,2R)-2-chlorocyclopropyl]-2,4,17-trimethyl-7-(trichloromethyl)-8,12-dioxa-19-azatricyclo[14.7.0.017,21]tricosa-2,14,21-triene-9,13,20-trione
Identifiers
CAS Number	1160939-11-6;
3D model (JSmol)	Interactive image; Interactive image;
ChemSpider	27024092;
PubChem CID	165365497;
CompTox Dashboard (EPA)	DTXSID301043854;
	InChI InChI=1S/C27H33Cl4NO5/c1-14-4-8-22(27(29,30)31)37-24(34)12-21(17-11-20(17)28)36-23(33)9-7-18-16(15(2)10-14)5-6-19-25(35)32-13-26(18,19)3/h6-7,9-10,14,16-18,20-22H,4-5,8,11-13H2,1-3H3,(H,32,35)/b9-7+,15-10+/t14-,16-,17?,18-,20-,21+,22-,26-/m1/s1 Key: DVSMDAZIABCDQH-XRDZMDRSSA-N; InChI=1S/C27H33Cl4NO5/c1-14-4-8-22(27(29,30)31)37-24(34)12-21(17-11-20(17)28)36-23(33)9-7-18-16(15(2)10-14)5-6-19-25(35)32-13-26(18,19)3/h6-7,9-10,14,16-18,20-22H,4-5,8,11-13H2,1-3H3,(H,32,35)/b9-7+,15-10+/t14-,16-,17-,18-,20-,21+,22-,26-/m1/s1 Key: DVSMDAZIABCDQH-DULMNHEISA-N;
	SMILES C[C@@H]\1CC[C@@H](OC(=O)C[C@H](OC(=O)/C=C/[C@@H]2[C@H](CC=C3[C@@]2(CNC3=O)C)/C(=C1)/C)C4C[C@H]4Cl)C(Cl)(Cl)Cl; C[C@@H]\1CC[C@@H](OC(=O)C[C@H](OC(=O)/C=C/[C@@H]2[C@H](CC=C3[C@@]2(CNC3=O)C)/C(=C1)/C)[C@@H]4C[C@H]4Cl)C(Cl)(Cl)Cl;
Properties
Chemical formula	C27H33Cl4NO5
Molar mass	593.36 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

Muironolide A is a tetrachloro polyketide discovered in 200 that has two unusual structural details: a hexahydro-1H-isoindolone-triketide ring and a trichlorocarbinol ester. It is suspected that it is the product of a sponge–microorganism (cyanobacteria) association.^[1] It was isolated from the marine sponge Phorbas sp.

Biosynthesis and synthesis

Muironolide A possibly has its biosynthetic route coming from PKS 1 responsible for forming the lactonic ring, with an amino acid residue, which forms the isoindole ring present in the molecule and successive enzymatic transformations of reduction, oxidation, cyclication, denaturation and additions of halogens ( Chlorine - Cl) result in the final molecule.^[2]

There are proposals for synthetic routes that elucidate the synthesis process. In 2015, Xiao and collaborators carried out the synthesis and structural revision of muironolide A molecules.^[2]

Biological activities

Muironolide A has already been tested for antineoplastic activity in 56 different models using different cell lines and did not provide biological activity in any of them.^[1] Phorbas sp. also produces the macrolides phorboxazoles A and B and phorbaside A, which do have antifungal and cytostatic activity.^[1]

References

^ ^a ^b ^c Dalisay, Doralyn S.; Morinaka, Brandon I.; Skepper†, Colin K.; Molinski, Tadeusz F. (May 15, 2009). "A Tetrachloro Polyketide Hexahydro-1H-isoindolone, Muironolide A, from the Marine Sponge Phorbas sp. Natural Products at the Nanomole Scale". Journal of the American Chemical Society. 131 (22): 7552–7553. doi:10.1021/ja9024929. PMID 19453148.
^ ^a ^b Xiao, Qing; Young, Kyle; Zakarian, Armen (2015-05-04). "Total Synthesis and Structural Revision of (+)-Muironolide A". Journal of the American Chemical Society. 137 (18): 5907–5910. doi:10.1021/jacs.5b03531. ISSN 0002-7863. PMID 25928351.

[:0-1] Dalisay, Doralyn S.; Morinaka, Brandon I.; Skepper†, Colin K.; Molinski, Tadeusz F. (May 15, 2009). "A Tetrachloro Polyketide Hexahydro-1H-isoindolone, Muironolide A, from the Marine Sponge Phorbas sp. Natural Products at the Nanomole Scale". Journal of the American Chemical Society. 131 (22): 7552–7553. doi:10.1021/ja9024929. PMID 19453148.

[:1-2] Xiao, Qing; Young, Kyle; Zakarian, Armen (2015-05-04). "Total Synthesis and Structural Revision of (+)-Muironolide A". Journal of the American Chemical Society. 137 (18): 5907–5910. doi:10.1021/jacs.5b03531. ISSN 0002-7863. PMID 25928351.

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