VLX600 - ≥98% , CAS No.327031-55-0

CAS: 327031-55-0 Cat. No.: V414284 Peso molecular: 317.35 Número EC: 816-332-1 PubChem CID: 6410104
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
AKOS000354357 | EN300-395210 | MFCD01305422 | Z2694498001 | AS-79800 | 6-methyl-3-{(2E)-2-[1-(pyridin-2-yl)ethylidene]hydrazinyl}-5H-[1,2,4]triazino[5,6-b]indole | SCHEMBL20518451 | Ethanone, 1-(2-pyridinyl)-, 2-(6-methyl-5H-1,2,4-triazino(5,6-b)indol-3-y
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
Size
Estado
Price
Qty
5mg
V414284-5mg
3
89,90US$
10mg
V414284-10mg
3
148,90US$
25mg
V414284-25mg
3
296,90US$
50mg
V414284-50mg
2
587,90US$
100mg
V414284-100mg
2
963,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

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

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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

Information

VLX600 VLX600 is a novel iron-chelating inhibitor of oxidative phosphorylation (OXPHOS) , potentiates the effect of radiation in tumor spheroids in a synergistic manner. VLX600 shows enhanced cytotoxic activity under conditions of nutrient starvation. VLX600 induces autophagy and mitochondrial inhibition with antitumor activity.


Targets

OXPHOS


In vitro

VLX600 shows enhanced cytotoxic activity under conditions of nutrient starvation. Mitochondrial inhibition with VLX600 has a direct antitumor effect in vitro while appearing to promote glycolysis through increased AKT signaling and glucose transporter expression. When combined with imatinib, VLX600 prevents imatinib-induced cell cycle escape and reduces p27 expression, leading to increased apoptosis when compared to imatinib alone.


In vivo

VLX600 induces the formation of autolysosomes in vivo. VLX600 displays tumour growth inhibition in vivo. When combined with imatinib, VLX600 reduces p27 expression and prevents imatinib-induced cell cycle escape, likely potentiating the antitumoral effects of Kit inhibition.


Cell Research(from reference)

Cell lines:human GIST-T1 cell line, human HG129 cell line, human GIST-882 cell line, 

Concentrations:2 μM, 6 μM, 12 μM 

Incubation Time:48–72h 

Specifications

Sinónimos
AKOS000354357 | EN300-395210 | MFCD01305422 | Z2694498001 | AS-79800 | 6-methyl-3-{(2E)-2-[1-(pyridin-2-yl)ethylidene]hydrazinyl}-5H-[1, 2, 4]triazino[5, 6-b]indole | SCHEMBL20518451 | Ethanone, 1-(2-pyridinyl)-, 2-(6-methyl-5H-1, 2, 4-triazino(5, 6-b)indol-3-y
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
VLX600 is a novel iron-chelating inhibitor of oxidative phosphorylation (OXPHOS), potentiates the effect of radiation in tumor spheroids in a synergistic manner. VLX600 shows enhanced cytotoxic activity under conditions of nutrient starvation. VLX600 indu
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Propiedades del producto
ALogP3.589
Recuento HBD2
Enlace rotable3
Nombres e identificadores
Pubchem Sid504764113
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764113
Sonrisas canónicasCC1=C2C(=CC=C1)C3=C(N2)N=C(N=N3)NN=C(C)C4=CC=CC=N4
IUPAC Name6-methyl-N-[(E)-1-pyridin-2-ylethylideneamino]-5H-[1,2,4]triazino[5,6-b]indol-3-amine
InChIKeyUQOSBPRTQFFUOA-SRZZPIQSSA-N
INCHI1S/C17H15N7/c1-10-6-5-7-12-14(10)19-16-15(12)22-24-17(20-16)23-21-11(2)13-8-3-4-9-18-13/h3-9H,1-2H3,(H2,19,20,23,24)/b21-11+
Isómeros SMILES CC1=C2C(=CC=C1)C3=C(N2)N=C(N=N3)N/N=C(\C)/C4=CC=CC=N4
PubChem CID 6410104
Peso molecular 317.35

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

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseIndoles and derivatives
SubclassIndoles
Intermediate Tree Nodes Not available
Direct ParentIndoles
Alternative Parents Pyridines and derivatives  Benzenoids  1,2,4-triazines  Pyrroles  Heteroaromatic compounds  Hydrazones  Azacyclic compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indole - 1,2,4-triazine - Benzenoid - Triazine - Pyridine - Heteroaromatic compound - Pyrrole - Azacycle - Hydrazone - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeFechaArticulo
C2512114Certificate of AnalysisAug 12, 2022 V414284
K2215482Certificate of AnalysisAug 12, 2022 V414284
K2215483Certificate of AnalysisAug 12, 2022 V414284
K2215484Certificate of AnalysisAug 12, 2022 V414284
K2215485Certificate of AnalysisAug 12, 2022 V414284
K2215487Certificate of AnalysisAug 12, 2022 V414284
Propiedades químicas y físicas
SolubilidadSolubility (25°C) In vitro DMSO: 13 mg/mL (40.96 mM); Water: ˂1 mg/mL Ethanol: ˂1 mg/mL
DMSO (mg/ml) Solubilidad máxima13
DMSO (mM) Solubilidad máxima40.9642350716874
Agua (mg/ml) Solubilidad máxima˂1
Punto de fusión (°C)>264°C (dec.)
Peso molecular317.300 g/mol
XLogP32.900
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass317.139 Da
Monoisotopic Mass317.139 Da
Topological Polar Surface Area91.700 Ų
Heavy Atom Count24
Formal Charge0
Complexity468.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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