deposited onadditionof MeOHwerefiltered off,and thefiltratewas passed  translation - deposited onadditionof MeOHwerefiltered off,and thefiltratewas passed  Indonesian how to say

deposited onadditionof MeOHwerefilt

deposited onadditionof MeOHwere
fi
ltered off,and the
fi
ltrate
was passed through a Sephadex LH-20 column (1.6×50 cm)
eluted with MeOH (200 ml; fraction of 10 ml) to afford twenty
fractions. The hydrolysates (fractions 10

13) were combined
on the basis of TLC behaviors, concentrated under vacuum and
the dried residue was chromatographed on silica gel column
(1.6×40 cm) with gradient CHCl
3
/MeOH (19:1 to 7:3; 1 l;
fraction of 10 ml) to afford the sapogenin
1a
(30 mg) and sugar
mixture (48 mg). The sapogenin
1a
(
Rf
=0.40) and the sugar
mixturewereobtainedfromthefractionsanalyzedbysilicagel-
TLC using the solvent systems (B) CHCl
3
/MeOH (95:5, v/v) and
(C)
n
-BuOH/Me
2
CO/H
2
O (4:5:1, v/v/v), respectively. A sample
of the sugar mixture (1 mg) was dissolved in pyridine (100
μ
l)
and analyzed by silica gel-TLC in the above described solvent
(C). After spraying with orcinol/H
2
SO
4
, glucose and galactose
gave blue spots at
Rf
values of 0.38 and 0.35, respectively.
(3
β
,5
α
,6
β
,25
R
)-Spirostan-3,6-diol (
1a
): Colorless needles
from benzene, mp 239

240 °C; [
α
]
D
25

72.5° (
c
0.5, CHCl
3
); IR
ν
max
(KBr): 3520, 3250 (OH), 2955, 2930, 2875, 2850 (CH),
1450, 1375, 1340, 1240, 1175, 1075, 1055, 1015, 1005, 980,
955, 915, 900, 860 cm

1
(intensity 915
b
900, 25
R
-spiroke-
tal); EIMS:
m
/
z
432 [M]
+
, 139 [C
9
H
15
O]
+
; The
1
H and
13
C
NMR (pyridine-
d
5
) data agreed well with those of literature
data
0/5000
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Results (Indonesian) 1: [Copy]
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deposit onadditionof MeOHwereFiltered, danFiltratedisahkan melalui kolom Sephadex LH-20 (1.6 × 50 cm)eluted dengan MeOH (200 ml; sebagian kecil dari 10 ml) mampu dua puluhpecahan. Hydrolysates (fraksi 10–13) digabungkanBerdasarkan perilaku TLC, terkonsentrasi di bawah vakum danresidu kering chromatographed pada kolom silika gel(1.6 × 40 cm) dengan gradien CHCl3/ MeOH (19:1 hingga 7:3; 1 l;sebagian kecil dari 10 ml) mampu sapogenin1a(30 mg) dan gulacampuran (48 mg). Sapogenin1a(RF= 0,40) dan gulamixturewereobtainedfromthefractionsanalyzedbysilicagel-TLC menggunakan sistem pelarut (B) CHCl3/ MeOH (95:5, v/v) dan(C)n-BuOH / saya2CO/H2O (4:5:1, v/v/v), masing-masing. Sampelgula campuran (1 mg) dibubarkan pada piridina (100Μl)dan dianalisis oleh silika gel-TLC dalam pelarut dijelaskan di atas(C). setelah penyemprotan dengan orcinol H2JADI4, glukosa dan galaktosamemberi bintik-bintik biru diRFnilai-nilai 0.38 dan 0,35, masing-masing.(3Β, 5Α, 6Β, 25R) - Spirostan - 3,6-diol ()1a): Berwarna jarumdari benzena, mp 239–240 ° C; [Α]D25–72.5°)c0,5, CHCl3); IRΝMax(KBr): 3520, 3250 (OH), 2955, 2930, 2875, 2850 (CH),1450, 1375, 1340, 1240, 1175, 1075, 1055, 1015, 1005, 980,955, 915, 900, 860 cm−1(intensitas 915b900, 25R-spiroke-Tal); EIMS:m/z432 [M]+, 139 [C9H15O]+; The1H dan13CNMR (piridina-d5) data setuju juga dengan orang-orang sastradata
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Results (Indonesian) 2:[Copy]
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disetorkan onadditionof MeOHwere
fi
disaring off, dan
fi
menyusup
disahkan melalui Sephadex LH-20 kolom (1,6 × 50 cm)
dielusi dengan MeOH (200 ml; fraksi 10 ml) untuk membeli dua puluh
fraksi. Hidrolisat (pecahan 10
-
13) digabungkan
atas dasar perilaku TLC, terkonsentrasi di bawah vakum dan
residu dikeringkan dikromatografi pada kolom silika gel
(1,6 × 40 cm) dengan gradien CHCl
3
/ MeOH (19: 1 sampai 7: 3 ; 1 l;
fraksi 10 ml) untuk membayar sapogenin
1a
(30 mg) dan gula
campuran (48 mg). The sapogenin
1a
(
Rf
= 0,40) dan gula
mixturewereobtainedfromthefractionsanalyzedbysilicagel-
TLC menggunakan sistem pelarut (B) CHCl
3
/ MeOH (95: 5, v / v) dan
(C)
n
-BuOH / Me
2
CO / H
2
O ( 4: 5: 1, v / v / v), masing-masing. Sebuah sampel
dari campuran gula (1 mg) dilarutkan dalam piridin (100
μ
l)
dan dianalisis dengan silika gel-TLC di atas dijelaskan pelarut
(C). Setelah penyemprotan dengan orsinol / H
2
SO
4
, glukosa dan galaktosa
memberi bintik-bintik biru di
Rf
nilai 0,38 dan 0,35, masing-masing.
(3
β
, 5
α
, 6
β
, 25
R
) -Spirostan-3,6-diol (
1a
) : jarum tak berwarna
dari benzena, mp 239
-
240 ° C; [
Α
]
D
25
-
72,5 ° (
c
0,5, CHCl
3
); IR
ν
max
(KBr): 3520, 3250 (OH), 2955, 2930, 2875, 2850 (CH),
1450, 1375, 1340, 1240, 1175, 1075, 1055, 1015, 1005, 980,
955, 915, 900 , 860 cm
-
1
(intensitas 915
b
900, 25
R
-spiroke-
tal); EIMS:
m
/
z
432 [M]
+
, 139 [C
9
H
15
O]
+
; The
1
H dan
13
C
NMR (pyridine-
d
5
) Data setuju dengan baik dengan orang-orang sastra
Data
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