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Cat. No.: HY-N8502

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Urdamycin A

Urdamycin A is an Angucycline-class Antibiotic. Urdamycin A can be derived from Streptomyces fradiae, S. fradiae Tu2717, and S. ardesiacus. Urdamycin A inhibits Gram-positive bacteria and Gram-negative bacteria. Urdamycin A lacks antifungal activity. Urdamycin A has anticancer activity against leukemia.

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CAS No.: 98474-21-6
Formule: C₄₃H₅₆O₁₇
Masse moléculaire:844.89

Stockage:

Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month

Urdamycin A Chemical Structure

CAS No.: 98474-21-6

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- IC₅₀ & Target
- Cellular Effect
- In Vitro
Chemical Information
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
Bioz

Activité biologique

Description

IC₅₀ & Target

^[1]

Microbial Metabolite

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Cellular Effect

Cell Line	Type	Value	Description	References
L1210	IC50	2.4 μg/mL	Antiproliferative activity against murine L1210 leukemia cells assessed as IC50 in proliferation assay. Antiproliferative activity against murine L1210 leukemia cells assessed as IC50 in proliferation assay.	3818439
L1210	IC50	0.55 μg/mL	Antiproliferative activity against murine L1210 leukemia stem cells assessed as IC50 in stem cell assay. Antiproliferative activity against murine L1210 leukemia stem cells assessed as IC50 in stem cell assay.	3818439

In Vitro

Anti-cancerBacterial InfectionFungal Infection

Anti-cancer

Urdamycin A inhibits proliferation of murine L1210 leukemia cells with an IC₅₀ of 2.4 μg/mL^[1].
Urdamycin A inhibits L1210 leukemia cells in a stem cell assay with an IC₅₀ of 0.55 μg/mL^[1].
Urdamycin A and derhodinosylurdamycin A exhibit IC₅₀ values of 0.55 μg/mL and 0.75 μg/mL, respectively, against murine L1210 leukemia stem cells^[2].

Bacterial Infection

Fungal Infection

Urdamycin A (1 mg/mL) shows antibacterial activity against Gram-positive and Gram-negative bacteria but no antifungal activity, with the largest inhibition (24 mm) against Bacillus subtilis⁺⁺ and Streptomyces viridochromogenes (Tü 57)^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Related Protocols :

Gram Staining of Tissue Sections

Chemical Information

CAS No. 98474-21-6
Appearance Solid
Masse moléculaire 844.89
Formule C₄₃H₅₆O₁₇
Color Light brown to brown
SMILES

O=C(C1=C(O)C([C@H]2C[C@H]([C@@H]([C@H](O2)C)O)O[C@@H]3O[C@H]([C@H](CC3)O[C@H]4C[C@H]([C@@H]([C@H](O4)C)O)O)C)=CC=C1C5=O)C(C=C[C@@]6(C[C@@](O)(CC7=O)C)O)=C5[C@]67O[C@@H]8O[C@H]([C@H](CC8)O)C
Structure Classification
- Antibiotics
Initial Source
- Microorganism
Streptomyces fradiae
Livraison

Room temperature in continental US; may vary elsewhere.

Stockage

Powder	-20°C	3 years
In solvent	-80°C	6 months
	-20°C	1 month

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (273 KB)
SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instruction de manipulation (2659 KB)

Références

[1]. DRAUTZ H, et al. Metabolic products of microorganisms. 234 Urdamycins, new angucycline antibiotics from Streptomyces fradiae I. Isolation, characterization and biological properties. The Journal of Antibiotics. 1986;39(12):1657-69. [Content Brief]

[2]. Acharya P P. Synthesis and Antitumor Activities of Aquayamycin and Analogues of Derhodinosylurdamycin A and Synthesis of S-Linked Trisaccharide Glycal of Derhodinosylurdamycin A[D]. University of Toledo, 2019.

[3]. Anh CV, et al. New angucycline glycosides from a marine-derived bacterium Streptomyces ardesiacus. International Journal of Molecular Sciences. 2022 Nov 9;23(22):13779.

[4]. Trefzer A, et al. Elucidation of the function of two glycosyltransferase genes (lanGT1 and lanGT4) involved in landomycin biosynthesis and generation of new oligosaccharide antibiotics. Chemistry & biology. 2001 Dec;8(12):1239-52.

[5]. Kirschning A, et al. Syntheses and biological evaluation of new glyco-modified angucyclin-antibiotics. Bioorganic & medicinal chemistry. 2000 Sep;8(9):2347-54.

Calculators

Calculateur de molarité

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

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Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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Keywords

MOQ

Minimum order quantity

100 mg

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Activité biologique
- Description
- IC₅₀ & Target
- In Vitro
Chemical Information
Pureté et documentation
Références

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Urdamycin A

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