Antimycin A3 - Moligand™, ≥98% , CAS No.522-70-3

CAS: 522-70-3 Cat. No.: A329432 Peso molecular: 520.57 Número EC: 208-335-6

COA

Saltar al final de la galería de imágenes

Antimycin A3 - Moligand™, ≥98% CAS No(522-70-3) by Aladdin Scientific

Saltar al comienzo de la galería de imágenes

Disponible para pedir

GRADE & PURITY Moligand™ ? ≥98%

Synonyms

(2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxybenzene)amido]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl 3-methylbutanoate | Purothionin AII | Blastmycin | 3-Methyl-butyric acid (2R,3S,6S,7R,8R)-8-butyl-3-(3-formylamino-2-hydroxy-benzoylamino)-2,6-dimeth

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general Specifications Propiedades del producto Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Calculadoras de soluciones Reseñas

🧪

Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Antimycin A3 is a homologue of the antimycin complex. Antimycin A3 is a more polar analogue of A1 and A2 and is a potent inhibitor of respiration by inhibiting the oxidation of ubiquinol to ubiquinone. Antimycin A3 exhibits broad biological activity as an antifungal, anthelmintic, insecticidal, antiviral and antitumor active.

Specifications

Sinónimos

(2R, 3S, 6S, 7R, 8R)-8-butyl-3-[(3-formamido-2-hydroxybenzene)amido]-2, 6-dimethyl-4, 9-dioxo-1, 5-dioxonan-7-yl 3-methylbutanoate | Purothionin AII | Blastmycin | 3-Methyl-butyric acid (2R, 3S, 6S, 7R, 8R)-8-butyl-3-(3-formylamino-2-hydroxy-benzoylamino)-2, 6-dimeth

Especificaciones y pureza

Moligand™, ≥98%

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

Moligand™

Pureza

≥98%

Propiedades del producto

pKa	pKₐ: 7.28 (Predicted), pKₐ: 1.29 (Predicted)
Datos Ki	Apoptosis regulator Bcl-2: Ki= 124 μM (human); Apoptosis regulator Bcl-W: Ki= 127 μM (human); Displacement of Flu-Bak peptide from recombinant antiapoptopic Bcl-XL protein: Ki= 127 μM (human)

Nombres e identificadores

Sonrisas canónicas	CCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C
IUPAC Name	[(2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxybenzoyl)amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] 3-methylbutanoate
InChIKey	PVEVXUMVNWSNIG-PDPGNHKXSA-N
INCHI	1S/C26H36N2O9/c1-6-7-9-18-23(37-20(30)12-14(2)3)16(5)36-26(34)21(15(4)35-25(18)33)28-24(32)17-10-8-11-19(22(17)31)27-13-29/h8,10-11,13-16,18,21,23,31H,6-7,9,12H2,1-5H3,(H,27,29)(H,28,32)/t15-,16+,18-,21+,23+/m1/s1
Isómeros SMILES	CCCC[C@@H]1[C@H]([C@@H](OC(=O)[C@H]([C@H](OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C
RTECS	NY1502900
Peso molecular	520.57
Reaxy-Rn	1277644
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1277644&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Clase Benzene and substituted derivatives
    - Subclass Benzoic acids and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Clase	Benzene and substituted derivatives
Subclass	Benzoic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Acylaminobenzoic acid and derivatives
Alternative Parents	Alpha amino acid esters N-acyl-alpha amino acids and derivatives Salicylamides Tricarboxylic acids and derivatives Anilides Benzamides N-arylamides Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids Fatty acid esters Vinylogous acids Secondary carboxylic acid amides Lactones Carboxylic acid esters Oxacyclic compounds Organic oxides Carbonyl compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Alpha-amino acid ester - Acylaminobenzoic acid or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Salicylamide - Salicylic acid or derivatives - Benzamide - Anilide - Tricarboxylic acid or derivatives - Benzoyl - N-arylamide - 1-hydroxy-4-unsubstituted benzenoid - Fatty acid ester - Phenol - Fatty acyl - Vinylogous acid - Carboxamide group - Carboxylic acid ester - Lactone - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Aromatic heteromonocyclic compound
Descripción	This compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Estructura 3D

Objetivos asociados (humanos)

BCL2 Tclin Apoptosis regulator Bcl-2 (1 Activities)

Discover Target: BCL2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

A498 (42825 Activities)

Lot Number	Certificate Type	Fecha	Articulo
I2512199	Certificate of Analysis	Sep 05, 2025	A329432
L2210131	Certificate of Analysis	Oct 28, 2022	A329432

Solubilidad	Soluble in ethanol, methanol, DMF, DMSO, and water (poorly).
Índice de refracción	n20D1.55 (Predicted)
Punto de ebullición (°C)	~745.5° C at 760 mmHg (Predicted)
Punto de fusión (°C)	170° C
Peso molecular	520.600 g/mol
XLogP3	4.200
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	9
Rotatable Bond Count	10
Exact Mass	520.242 Da
Monoisotopic Mass	520.242 Da
Topological Polar Surface Area	157.000 Å²
Heavy Atom Count	37
Formal Charge	0
Complexity	818.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Antimycin A3 - Moligand™, ≥98% , CAS No.522-70-3

Why this grade

Storage & shipping

Quality documents

Literature proof

Descripción general

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Reseñas de cliente

Need help choosing the grade?

View related series