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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
144525-81-5
Murrayanol
CC1=CC2=C(C=C1OC)NC3=C2C=CC(=C3CC=C(C)CCC=C(C)C)O
C
24
H
29
NO
2
363.5
HPLC≥95%
Click to inquire
84575-13-3
Bakuchalcone
CC(C)(C1CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O
C
20
H
20
O
5
340.4
HPLC≥95%
Click to inquire
350221-50-0
Brosimacutin G
CC(C)(C1C(C2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)O
C
20
H
20
O
6
356.4
HPLC≥95%
Click to inquire
63807-86-3
Erythrinin A
CC1(C=CC2=CC3=C(C=C2O1)OC=C(C3=O)C4=CC=C(C=C4)O)C
C
20
H
16
O
4
320.3
HPLC≥95%
Click to inquire
252351-96-5
Lucidal
CC(CCC=C(C)C=O)C1CCC2(C1(CCC3=C2C(=O)CC4C3(CCC(C4(C)C)O)C)C)C
C
30
H
46
O
3
454.7
HPLC≥95%
Click to inquire
879324-75-1
Prionoid B
CC1=C2C(=O)C(OC3=C2C(=CC(=C3O)C(C)C)C=C1)C=C(C)C
C
20
H
22
O
3
310.4
HPLC≥95%
Click to inquire
58311-20-9
Kusunokinin
COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC
C
21
H
22
O
6
370.4
HPLC≥95%
Click to inquire
84304-92-7
Rabdosin B
CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)OC(=O)C)(C)C
C
24
H
32
O
8
448.5
HPLC≥95%
Click to inquire
63303-42-4
3beta-[[(E)-3-(4-Hydroxyphenyl)propenoyl]oxy]-2alpha-hydroxyurs-12-ene-28-oic acid
CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O
C
39
H
54
O
6
618.8
HPLC≥95%
Click to inquire
189272-68-2
Eucalyptolic acid
CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)C)C)C2C1)C)C(=O)O)C
C
40
H
56
O
7
648.9
HPLC≥95%
Click to inquire
144525-81-5
Murrayanol
Murrayanol
C
24
H
29
NO
2
363.5
84575-13-3
Bakuchalcone
Bakuchalcone
C
20
H
20
O
5
340.4
350221-50-0
Brosimacutin G
Brosimacutin G
C
20
H
20
O
6
356.4
63807-86-3
Erythrinin A
Erythrinin A
C
20
H
16
O
4
320.3
252351-96-5
Lucidal
Lucidal
C
30
H
46
O
3
454.7
879324-75-1
Prionoid B
Prionoid B
C
20
H
22
O
3
310.4
58311-20-9
Kusunokinin
Kusunokinin
C
21
H
22
O
6
370.4
84304-92-7
Rabdosin B
Rabdosin B
C
24
H
32
O
8
448.5
63303-42-4
3beta-[[(E)-3-(4-Hydroxyphenyl)propenoyl]oxy]-2alpha-hydroxyurs-12-ene-28-oic acid
Jacoumaric acid
C
39
H
54
O
6
618.8
189272-68-2
Eucalyptolic acid
Eucalyptolic acid
C
40
H
56
O
7
648.9
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