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XANTHOQUINODIN A1

Product Name
XANTHOQUINODIN A1
CAS No.
151063-27-3
Chemical Name
XANTHOQUINODIN A1
Synonyms
XANTHOQUINODIN A1;(4R,4aS,7aS,15R)-rel-2,3,4,7,8,13,15,17-octahydro-1,4,12,14,16-pentahydroxy-10-methyl-8,13,17-trioxo-4aH-7a,15-ethenonaphtho[2′,3′:4,5]cyclohepta[1,2-b]xanthene-4a-carboxylic acid, methyl ester;4aH-7a,15-Ethenonaphtho[2',3':4,5]cyclohepta[1,2-b]xanthene-4a-carboxylic acid, 2,3,4,7,8,13,15,17-octahydro-1,4,12,14,16-pentahydroxy-10-methyl-8,13,17-trioxo-, methyl ester, (4R,4aS,7aS,15R)-rel-
CBNumber
CB2708023
Molecular Formula
C31H24O11
Formula Weight
572.52
MOL File
151063-27-3.mol
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XANTHOQUINODIN A1 Property

Boiling point:
859.6±65.0 °C(Predicted)
Density 
1.74±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Dichloromethane: soluble,DMSO: soluble,Ethanol: soluble,Methanol: soluble
form 
A solid
pka
4.50±1.00(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
28792
Product name
Xanthoquinodin A1
Packaging
1mg
Price
$194
Updated
2024/03/01
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XANTHOQUINODIN A1 Chemical Properties,Usage,Production

Uses

Xanthoquinodin A1 is an anticoccidial antibiotic having a new xanthone-anthraquinone conjugate system[1].

Biological Activity

Xanthoquinodin A1 is a fungal metabolite that has been found in Humicola and has diverse biological activities.1,2 It inhibits E. tenella schizont formation in BHK-21 cells with a minimum effective concentration (MEC) value of 0.02 μg/ml.1 Xanthoquinodin A1 is active against B. subtilis, M. luteus, S. aureus, A. laidlawii, and B. fragilis in a disc assay when used at a concentration of 1 mg/ml. It is also active against B. cereus (MIC = 0.44 μM).2 Xanthoquinodin A1 is cytotoxic to KB, MCF-7, and NCI H187 cancer cells.

References

1.Tabata, N., Suzumura, Y., Tomoda, H., et al.Xanthoquinodins, new anticoccidial agents produced by Humicola sp. Production, isolation and physico-chemical and biological propertiesJ. Antibiot. (Tokyo)46(5)749-755(1993) 2.Tantapakul, C., Promgool, T., Kanokmedhakul, K., et al.Bioactive xanthoquinodins and epipolythiodioxopiperazines from Chaetomium globosum 7s-1, an endophytic fungus isolated from Rhapis cochinchinensis (Lour.) MartNat. Prod. Res.34(4)494-502(2020)

XANTHOQUINODIN A1 Preparation Products And Raw materials

Raw materials

Preparation Products

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XANTHOQUINODIN A1 Suppliers

Shanghai Haozhixiang Biotechnology Co., Ltd
Tel
526763801 13301653310
Fax
+86-21-51619052
Email
526763801@qq.com
Country
China
ProdList
9279
Advantage
55
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11218
Advantage
58
Chengdu Jiuding Chemical Technology Co., Ltd. - Song Bo
Tel
18584079237
Email
312074905@qq.com
Country
China
ProdList
2513
Advantage
58
Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
11973
Advantage
58
Guangzhou Yaoguang Technology Co., Ltd.
Tel
13020159086
Email
yangjue@ygfuture.com
Country
China
ProdList
424
Advantage
58
TargetMol Chemicals Inc.
Tel
15002134094
Email
marketing@targetmol.cn
Country
China
ProdList
29423
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58
Hubei Danding Pharmaceutical Technology Co., Ltd
Tel
17701422019
Email
1559451077@qq.com
Country
China
ProdList
8167
Advantage
58
Cayman Chemical Company
Tel
800-364-9897
Email
sales@caymanchem.com
Country
China
ProdList
6838
Advantage
58
Biosynth Biological Technology (Suzhou) Co Ltd
Tel
51288865780
Email
sales@biosynth.com
Country
China
ProdList
6051
Advantage
58
Guangzhou Qingyan Biotechnology Co., Ltd.
Tel
19802084049
Country
CHINA
ProdList
171
Advantage
58
Shenzhen Campbell Biotechnology Co., Ltd.
Tel
18028747627
Country
CHINA
ProdList
191
Advantage
58

151063-27-3, XANTHOQUINODIN A1Related Search:


  • XANTHOQUINODIN A1
  • 4aH-7a,15-Ethenonaphtho[2',3':4,5]cyclohepta[1,2-b]xanthene-4a-carboxylic acid, 2,3,4,7,8,13,15,17-octahydro-1,4,12,14,16-pentahydroxy-10-methyl-8,13,17-trioxo-, methyl ester, (4R,4aS,7aS,15R)-rel-
  • (4R,4aS,7aS,15R)-rel-2,3,4,7,8,13,15,17-octahydro-1,4,12,14,16-pentahydroxy-10-methyl-8,13,17-trioxo-4aH-7a,15-ethenonaphtho[2′,3′:4,5]cyclohepta[1,2-b]xanthene-4a-carboxylic acid, methyl ester
  • 151063-27-3