Beauvericin, 98%

Name: Beauvericin, 98% | 26048-05-5
Brand: J&K Chemical
SKU: JK924708_10_MG
Price: 580.0 USD
Availability: InStock

Cat. No JK924708_10_MG

Vendor: J&K Chemical

Product Information

Product Name

Beauvericin, 98%

Brand Name

J&K

Product Number

924708

CAS

26048-05-5

Molecular Formula

C45H57N3O9

Molecular Weight

783.95

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

cyclo(D-α-Hydroxyisovaleryl-L-N-methyl-Phe)3

PubChem CID

3007984

IUPAC Name

(3S,6R,9S,12R,15S,18R)-3,9,15-tribenzyl-4,10,16-trimethyl-6,12,18-tri(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

InChI Key

GYSCAQFHASJXRS-FFCOJMSVSA-N

SMILES

CC(C)C@@H1C(=O)N(C@H(C(=O)OC@@H(C(=O)N(C@H(C(=O)OC@@H(C(=O)N(C@H(C(=O)O1)CC2=CC=CC=C2)C)C(C)C)CC3=CC=CC=C3)C)C(C)C)CC4=CC=CC=C4)C

Properties

Melting Point

150

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

Beauvericin disrupts G2/M transition and induces meiotic arrest during mouse oocyte maturation

Publication Name: Reproductive toxicology (Elmsford, N.Y.)

Publication Date: 2025-10

DOI: 10.1016/j.reprotox.2025.109032

A putative ABC transporter gene, CcT1 , is involved in beauvericin synthesis, conidiation, and oxidative stress resistance in Cordyceps chanhua

Publication Name: Microbiology Spectrum

Publication Date: 2025-07

DOI: 10.1128/spectrum.03425-24

Fumonisin production and symptom development in onion (Allium cepa) inoculated with Fusarium proliferatum

Publication Name: Mycotoxin Research

Publication Date: 2025-06-14

DOI: 10.1007/s12550-025-00595-0

Evaluation of Beauvericin’s activity and mode of action against all life stages of L. tropica for cutaneous Leishmaniasis therapy

Publication Name: Frontiers in Cellular and Infection Microbiology

Publication Date: 2025-06-10

DOI: 10.3389/fcimb.2025.1599766

The mycotoxin Beauvericin is an uncompetitive inhibitor of Cathepsin B

Publication Name: Protein science : a publication of the Protein Society

Publication Date: 2025-05-24

DOI: 10.1002/pro.70173

Beauvericin, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Beauvericin disrupts G2/M transition and induces meiotic arrest during mouse oocyte maturation

A putative ABC transporter gene, CcT1 , is involved in beauvericin synthesis, conidiation, and oxidative stress resistance in Cordyceps chanhua

Fumonisin production and symptom development in onion (Allium cepa) inoculated with Fusarium proliferatum

Evaluation of Beauvericin’s activity and mode of action against all life stages of L. tropica for cutaneous Leishmaniasis therapy

The mycotoxin Beauvericin is an uncompetitive inhibitor of Cathepsin B

Beauvericin, 98%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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Beauvericin, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Beauvericin disrupts G2/M transition and induces meiotic arrest during mouse oocyte maturation

A putative ABC transporter gene, CcT1 , is involved in beauvericin synthesis, conidiation, and oxidative stress resistance in Cordyceps chanhua

Fumonisin production and symptom development in onion (Allium cepa) inoculated with Fusarium proliferatum

Evaluation of Beauvericin’s activity and mode of action against all life stages of L. tropica for cutaneous Leishmaniasis therapy

The mycotoxin Beauvericin is an uncompetitive inhibitor of Cathepsin B

Beauvericin, 98%

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2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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