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MAKISTERONE A 3-ACETATE

Year of first isolation: 2024
Formula:C30H48O8
Molecular weight:536
Occurence in plants:
Cyanotis arachnoidea [Commelinaceae] » Images of Cyanotis arachnoidea Wikipedia: Cyanotis arachnoidea [Commelinaceae]
Occurence in animals:
 
MAKISTERONE A 3-ACETATE

STRUCTURE DESCRIPTORS

Isomeric SMILES
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C[C@@]12[C@@](C(C=C3C2CC[C@@]4(C)[C@@]3(O)CC[C@]4([H])[C@](C)([C@H](O)C[C@@H](C)C(C)(O)C)O)=O)([H])C[C@@H](OC(C)=O)[C@@H](O)C1 » JSMol: View in 3D
IUPAC Name(2S,3R,5R,10R,13R,14S,17S)-2,14-dihydroxy-10,13-dimethyl-6-oxo-17-((2R,3R,5R)-2,3,6-trihydroxy-5,6-dimethylheptan-2-yl)-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate
CAS-RN 
PubChem CID 
InChiKey
[ ChemIDPlus: search ]
CVJYYQQNQIKRIR-YSBOLLMGSA-N
InChIInChI=1S/C30H48O8/c1-16(26(3,4)35)12-25(34)29(7,36)24-9-11-30(37)19-13-21(32)20-14-23(38-17(2)31)22(33)15-27(20,5)18(19)8-10-28(24,30)6/h13,16,18,20,22-25,33-37H,8-12,14-15H2,1-7H3/t16-,18?,20+,22+,23-,24+,25-,27-,28-,29-,30-/m1/s1

MASS SPECTRUM

HRESIMS (positive ion mode) m/z 537.343 [M+H]+

CARBON NMR

PROTON NMR

C5D5N
0139.2
0266.6
0371.8
0430.2
0552.5
06202.4
07122.3
08167.0
0934.9
1039.1
1121.6
1232.5
1348.6
1484.6
1532.3
1621.9
1750.5
1818.4
1924.8
2077.4
2122.1
2275.2
2335.1
2442.3
2572.6
2627.0
2728.7
2815.9
C=O171.1
CH3CO21.6
C5D5N
01-Ha1.83 (m)
01-Hb2.25 (m)
02-Ha4.32 (m)
03-He5.51 (m)
04-Ha1.81 (m)
04-Hb1.97 (m)
05-H2.69 (dd, 2.7, 9.0)
07-H6.28 (d, 1.8)
09-H3.60 (br, t)
11-Ha2.55 (m)
11-Hb1.85 ((m)
12-Ha2.57 (m)
12-Hb2.62 (m)
15-Ha2.21 (m)
15-Hb1.90 (m)
16-Ha2.14 (m)
16-Hb2.14 (m)
17-H2/99 (br, t)
18-Me1.26 (s)
19-Me1.10 (s)
21-Me1.61 (s)
22-H4.01 (d, 7.4)
23-Ha2.16 (m)
23-Hb1.59 (m)
26-Me1.35 (s)
27-Me1.33 (s)
28-Me1.09 (S)
CH3CO2.01 (S)

PHYSICAL PROPERTIES

M.P.— °C
[α]D20+ (c ; MeOH)
IR (KBr) ν max (cm-1)3416, 1727, 1654, 1067
UV (MeOH) λ max (log ε)nm (-)

CHROMATOGRAPHY

TLC
GLC
HPTLC
HPLC

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationSU, F-Y. et al. (2024) Zhongguo Zhong Yao Za Zhi 49, 6165-6172 Search more

see Important notice
© Université Pierre & Marie Curie, Paris 6, France
© Institute of Organic Chemistry and Biochemistry, Academy of Sciences, Prague, Czech Republic
© Institut National de la Recherche Agronomique, Versailles, France
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