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Kibdelone C

Product Name
Kibdelone C
CAS No.
934464-79-6
Chemical Name
Kibdelone C
Synonyms
Kibdelone C;2H-[1]Benzopyrano[2',3':6,7]naphth[2,1-g]isoquinoline-1,14-dione, 4-chloro-6,7,10,11,12,13-hexahydro-5,10,12,13,15,16-hexahydroxy-8-methoxy-2-methyl-3-propyl-, (10S,12S,13R)-
CBNumber
CB02703741
Molecular Formula
C29H28ClNO10
Formula Weight
585.99
MOL File
934464-79-6.mol
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Kibdelone C Property

Melting point:
265-267 °C(Solv: benzene (71-43-2))
Boiling point:
968.8±65.0 °C(Predicted)
Density 
1.71±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble
form 
A solid
pka
6.44±0.70(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
21525
Product name
Kibdelone C
Purity
≥95%
Packaging
1mg
Price
$285
Updated
2024/03/01
TRC
Product number
K570518
Product name
KibdeloneC
Packaging
2.5mg
Price
$475
Updated
2021/12/16
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Kibdelone C Chemical Properties,Usage,Production

Description

Kibdelone C is a member of a family of natural heterocyclic polyketides first isolated from a soil actinomycete, Kibdelosporangium. Kibdelones have been described as having potent and selective cytotoxicity against a panel of human tumor cell lines, and kibdelone C has low nanomolar effectiveness in these assays. Kibdelone C disrupts the actin cytoskeleton without directly binding actin or affecting its polymerization in vitro.

Uses

Kibdelone C is the major analogue of a potent antitumour complex isolated from Kibdelosporangium sp.. Structurally, kibdelone C is related to lysolipin and albofungin, however no comparative investigation of this class has been reported. The mode of action and pharmacology of the kibdelones has received little attention.

Uses

Kibdelone C is the major analogue of a potent antitumor complex isolated from Kibdelosporangium sp.. Structurally, kibdelone C is related to lysolipin and albofungin, however no comparative investigation of this class has been reported. The mode of action and pharmacology of the kibdelones has received little attention.

Uses

Kibdelone C is the major analogue of a potent antitumor complex.

References

[1] RANJALA RATNAYAKE. Kibdelones: Novel Anticancer Polyketides from a Rare Australian Actinomycete[J]. Chemistry - A European Journal, 2007, 13 5: 1610-1619. DOI: 10.1002/chem.200601236
[2] JANJIRA RUJIRAWANICH. Synthesis and Biological Evaluation of Kibdelone C and Its Simplified Derivatives[J]. Journal of the American Chemical Society, 2016, 138 33: 10561-10570. DOI: 10.1021/jacs.6b05484

Kibdelone C Preparation Products And Raw materials

Raw materials

Preparation Products

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Kibdelone C Suppliers

Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Country
China
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4587
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Novachemistry
Tel
44-20819178-90 02081917890
Fax
(0)2080432064
Email
info@novachemistry.com
Country
United Kingdom
ProdList
4381
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58
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6777
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58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
57422
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58
BOC Sciences
Tel
16314854226; +16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19654
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58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32435
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58
Meng Cheng Technology (Shanghai) Co., LTD
Tel
400-820-6829
Email
sales@mitachieve.com
Country
China
ProdList
8860
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58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24961
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58
Shanghai Saikerui Biotechnology Co. , Ltd.
Tel
021-58000709 15900491054
Email
info@scrbio.com
Country
China
ProdList
9881
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Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
11973
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58

934464-79-6, Kibdelone CRelated Search:


  • Kibdelone C
  • 2H-[1]Benzopyrano[2',3':6,7]naphth[2,1-g]isoquinoline-1,14-dione, 4-chloro-6,7,10,11,12,13-hexahydro-5,10,12,13,15,16-hexahydroxy-8-methoxy-2-methyl-3-propyl-, (10S,12S,13R)-
  • 934464-79-6