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Caerulomycin A, with the chemical formula 21802-37-9, is a chemically novel and potent immunosuppressive agent derived from the rare and unusual antibiotic Caerulomycin. It was discovered in 1959 from a strain of Streptomyces caeruleus isolated in Canada. CAERULOMYCIN A contains a core 2,2'-bispyridyl with an oxime substituent and exhibits a broad spectrum of bioactivity. Caerulomycin A is known for its ability to suppress T cell activation and IFNγ secretion both in vitro and in vivo. It also induces the expansion of regulatory T cells by interfering with IFNγ-induced STAT1 signaling.

21802-37-9

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21802-37-9 Usage

Uses

Used in Pharmaceutical Industry:
Caerulomycin A is used as an immunosuppressive agent for its ability to suppress T cell activation and IFNγ secretion. This property makes it a valuable compound in the development of treatments for autoimmune diseases and conditions requiring immune modulation.
Used in Antifungal Applications:
Caerulomycin A is used as an antifungal agent due to its activity against fungi. This application can be beneficial in the development of treatments for various fungal infections.
Used in Antiprotozoan Applications:
Caerulomycin A is also used as an antiprotozoan agent, as it demonstrates activity against some protozoans. This can be useful in the treatment of protozoan infections, such as those caused by parasites.
Used in Antibacterial Applications:
Although its activity against bacteria is weak, Caerulomycin A can still be used as a weak antibacterial agent. This may be beneficial in certain situations where a broad-spectrum approach to treatment is necessary.
Used in Research and Development:
Caerulomycin A's unique chemical structure and broad spectrum of bioactivity make it an interesting compound for research and development in the pharmaceutical and biotechnology industries. It can be used as a starting point for the development of new drugs and therapies targeting various diseases and conditions.

References

1) Singla?et al. (2014),?Caerulomycin A suppresses immunity by inhibiting T cell activity; PLoS One,?9(10)?e107051 2) Gurram?et al. (2014),?Caerulomycin A enhances transforming growth factor-beta (TGF-β)-Smad3 protein signaling by suppressing interferon-gamma (IFN-γ)-signaling to expand regulatory T cells (Tregs); J. Biol. Chem.?289?17515

Check Digit Verification of cas no

The CAS Registry Mumber 21802-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,0 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21802-37:
(7*2)+(6*1)+(5*8)+(4*0)+(3*2)+(2*3)+(1*7)=79
79 % 10 = 9
So 21802-37-9 is a valid CAS Registry Number.

21802-37-9 Well-known Company Product Price

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  • Sigma

  • (C6374)  Caerulomycin A  from Streptomyces caeruleus, ≥98% (HPLC)

  • 21802-37-9

  • C6374-1MG

  • 4,668.30CNY

  • Detail

21802-37-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name caerulomycin A

1.2 Other means of identification

Product number -
Other names CERULOMYCIN

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21802-37-9 SDS

21802-37-9Downstream Products

21802-37-9Relevant articles and documents

Facile one-pot direct arylation and alkylation of nitropyridine N -oxides with grignard reagents

Zhang, Fang,Duan, Xin-Fang

, p. 6102 - 6105 (2012/01/06)

Facile arylation and alkylation of nitropyridine N-oxides were developed through the reactions of Grignard reagents with nitropyridine N-oxides. For the same 4-nitropyridine N-oxide, arylation occurred at the 2- (or 6-) position, whereas alkylation occurred at the 3-position in an adjustably site-selective manner. The cooperative action of the two groups was discovered in the reactions of 3-nitropyridine N-oxides. This protocol can find wide applications in building various pyridine compounds as illustrated in total syntheses of Emoxipin and Caerulomycin A and E.

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