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Petromurin C

Product Name
Petromurin C
CAS No.
194608-29-2
Chemical Name
Petromurin C
Synonyms
Petromurin C;3-[4-(1H-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-1H-indol-5-ol;1H-Indol-5-ol, 3-[4-(1H-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-
CBNumber
CB84666787
Molecular Formula
C26H24N2O5
Formula Weight
444.48
MOL File
194608-29-2.mol
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Petromurin C Property

Boiling point:
610.7±55.0 °C(Predicted)
Density 
1.309±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
form 
A solid
pka
9.60±0.40(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
25089
Product name
Petromurin C
Purity
≥95%
Packaging
500μg
Price
$121
Updated
2024/03/01
Cayman Chemical
Product number
25089
Product name
Petromurin C
Purity
≥95%
Packaging
2.5mg
Price
$543
Updated
2024/03/01
AK Scientific
Product number
1545EA
Product name
CID85743767
Packaging
2.5mg
Price
$702
Updated
2021/12/16
aablocks
Product number
AA01EQ4L
Product name
3-[4-(1H-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-1H-indol-5-ol
Purity
≥95%
Packaging
2.5mg
Price
$608
Updated
2021/12/16
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Petromurin C Chemical Properties,Usage,Production

Description

Petromurin C is a bis-indolyl benzenoid fungal metabolite originally isolated from the ascostromata of P. muricatus. It is cytotoxic to NS-1 mouse myeloma cells (IC50 = 33 μg/ml) and has activity against T. foetus in vitro (IC50 = 100 μg/ml).

Uses

Petromurin C is a bisindolylbenzenoid compound isolated from the ascostromata of Petromycesmuricatus. Petromurin C induces protective autophagy and apoptosis in FLT3-ITD-positive AML[1][2].

References

[1] Mikiko Ooike, et al. Bisindolylbenzenoids from ascostromata of Petromycesmuricatus.
[2] Ha YN, et al. Petromurin C Induces Protective Autophagy and Apoptosis in FLT3-ITD-Positive AML: Synergy with Gilteritinib. Mar Drugs. 2020;18(1):57. DOI:10.3390/md18010057

Petromurin C Preparation Products And Raw materials

Raw materials

Preparation Products

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Petromurin C Suppliers

China 8 United States 3 Global 11
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6777
Advantage
58
BOC Sciences
Tel
16314854226; +16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19654
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32435
Advantage
58
Meng Cheng Technology (Shanghai) Co., LTD
Tel
400-820-6829
Email
sales@mitachieve.com
Country
China
ProdList
8860
Advantage
58
Shanghai Saikerui Biotechnology Co. , Ltd.
Tel
021-58000709 15900491054
Email
info@scrbio.com
Country
China
ProdList
9881
Advantage
58
Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
11973
Advantage
58
TargetMol Chemicals Inc.
Tel
15002134094
Email
marketing@targetmol.cn
Country
China
ProdList
29257
Advantage
58
Shanghai Weiyite Biotechnology Co., Ltd
Tel
15317051735
Email
zhaojing@wytsci.com
Country
China
ProdList
9980
Advantage
58
Cayman Chemical Company
Tel
800-364-9897
Email
sales@caymanchem.com
Country
China
ProdList
6838
Advantage
58

194608-29-2, Petromurin CRelated Search:


  • Petromurin C
  • 3-[4-(1H-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-1H-indol-5-ol
  • 1H-Indol-5-ol, 3-[4-(1H-indol-3-yl)-2,3,5,6-tetramethoxyphenyl]-
  • 194608-29-2