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BOC Sciences
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Products Intro: |
Product Name:Nocardamine CAS:26605-16-3 Purity:>=95% Remarks:Nocardamine, derived from Nocardia sp., has anti-mycobacterium activity.
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NOCARDAMINE manufacturers
- Nocardamine
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- $273.00 / 1mg
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2024-10-24
- CAS:26605-16-3
- Min. Order:
- Purity:
- Supply Ability: 10g
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| NOCARDAMINE Basic information |
Product Name: | NOCARDAMINE | Synonyms: | NOCARDAMINE;PROFERRIOXAMIN E;deferrioxamine E;1,12,23-Trihydroxy-1,6,12,17,23,28-hexaazacyclotritriacontane-2,5,13,16,24,27-hexone;6,17,28-Trihydroxy-1,6,12,17,23,28-hexaazacyclotritriacontane-2,5,13,16,24,27-hexaone;Desferri-ferrioxamine E;Desferrioxamine E;Nocardamin | CAS: | 26605-16-3 | MF: | C27H48N6O9 | MW: | 600.7 | EINECS: | | Product Categories: | | Mol File: | 26605-16-3.mol | |
| NOCARDAMINE Chemical Properties |
Melting point | 192-195° | density | 1.162±0.06 g/cm3(Predicted) | storage temp. | -20°C | solubility | Soluble in DMSO (5 mg/ml) | form | solid | pka | 8?+-.0.20(Predicted) | color | Off-white | Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months. |
| NOCARDAMINE Usage And Synthesis |
Description | Nocardamine is a ferrioxamine siderophore that has been found in Streptomyces and has diverse biological activities. It chelates iron in a chrome azurol S assay (IC50 = 9.9 μM). Nocardamine inhibits M. smegmatis and M. bovis biofilm formation (MIC = 10 μM for both), an effect that can be reversed by iron. It is cytotoxic to T47D, SK-MEL-5, SK-MEL-28, and RPMI-7951 cancer cells (IC50s = 6, 18, 12, and 14 μM, respectively). Nocardamine also induces morphological changes in BM-N4 insect cells. | Uses | Nocardamine is a cyclic siderophore. | Definition | ChEBI: A cyclic hydroxamic acid siderophore that is produced by several bacterial species and exhibits antitumour activity. | storage | +4°C | References | Normant et al. (2020), Nocardamine-Dependent Iron Uptake in Pseudomonas aeruginosa: Exclusive Involvement of the FoxA Outer Membrane Transporter; ACS Chem. Biol. 15 2741
Ueki et al. (2009), Nocardamin Production by Streptomyces avermitilis; Actinomycetologica 23 34
Yan et al. (2021), Ferroptosis: mechanisms and links with diseases; Signal Transduct. Target Ther. 6 49
Kalinovskaya et al. (2011), Marine isolate Citricoccus sp. KMM 3890 as a source of a cyclic siderophore nocardamine with antitumor activity; Res. 166 654
Mahmud et al. (2022), Bioactivities and Mode of Actions of Dibutyl Phthalates and Nocardamine from Streptomyces sp. H11809; Molecules 27 2292 |
| NOCARDAMINE Preparation Products And Raw materials |
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