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Plant Sources
Structural Classes
Microbial Sources
Flagship Varieties
Synthetic Compounds
All
CAS No.
NAME
Molecular Formula
Molecular Weight
Purity
Price
2D Structure
99217-75-1
Mulberrofuran G pentaacetate
CC1=CC2C3C(C1)C4=C(C=C(C=C4)OC(=O)C)OC3(OC5=C2C(=CC(=C5)C6=CC7=C(O6)C=C(C=C7)OC(=O)C)OC(=O)C)C8=C(C=C(C=C8)OC(=O)C)OC(=O)C
C
44
H
36
O
13
772.7
HPLC≥98%
Click to inquire
942480-13-9
CID 124222284
CC1=CC(=O)OC(C1)C=C(C)CCCC(C)C2=CC(=O)C(O2)(C)C
C
20
H
28
O
4
332.4
HPLC≥98%
Click to inquire
111518-95-7
Nyasicol
C1=CC(=C(C=C1C#CCC(C(C2=CC(=C(C=C2)O)O)O)O)O)O
C
17
H
16
O
6
316.30
HPLC≥98%
Click to inquire
119318-15-9
24-Hydroxy-beta-amyrin
CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C
C
30
H
50
O
2
442.7
HPLC≥98%
Click to inquire
190381-82-9
Orientanol A
CC(C)(C(CC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC)O)O
C
21
H
24
O
7
388.4
HPLC≥98%
Click to inquire
76122-57-1
Phaseollidin hydrate
CC(C)(CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)O
C
20
H
22
O
5
342.4
HPLC≥98%
Click to inquire
157659-20-6
Prenylpiperitol
CC(=CCOC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC)C
C
25
H
28
O
6
424.5
HPLC≥98%
Click to inquire
134476-74-7
CID 91895427
CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CCC3C4(CCC(O4)C(=C)C)C)C)C
C
30
H
48
O
3
456.7
HPLC≥98%
Click to inquire
54854-91-0
Sanshodiol
COC1=C(C=CC(=C1)C2C(C(CO2)CC3=CC4=C(C=C3)OCO4)CO)O
C
20
H
22
O
6
358.4
HPLC≥98%
Click to inquire
905929-95-5
Scutebarbatine B
CC1=CCCC2C1(C(C(C(C2(C)C=CC3=CC(=O)OC3)(C)O)OC(=O)C4=CC=CC=C4)OC(=O)C5=CN=CC=C5)C
C
33
H
35
NO
7
557.6
HPLC≥98%
Click to inquire
99217-75-1
Mulberrofuran G pentaacetate
Mulberrofuran G pentaacetate
C
44
H
36
O
13
772.7
942480-13-9
CID 124222284
Nemoralisin
C
20
H
28
O
4
332.4
111518-95-7
Nyasicol
Nyasicol
C
17
H
16
O
6
316.30
119318-15-9
24-Hydroxy-beta-amyrin
Olean-12-ene-3,24-diol
C
30
H
50
O
2
442.7
190381-82-9
Orientanol A
Orientanol A
C
21
H
24
O
7
388.4
76122-57-1
Phaseollidin hydrate
Phaseollidin hydrate
C
20
H
22
O
5
342.4
157659-20-6
Prenylpiperitol
Prenylpiperitol
C
25
H
28
O
6
424.5
134476-74-7
CID 91895427
Richenoic acid
C
30
H
48
O
3
456.7
54854-91-0
Sanshodiol
Sanshodiol
C
20
H
22
O
6
358.4
905929-95-5
Scutebarbatine B
Scutebarbatine B
C
33
H
35
NO
7
557.6
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