VLX600 - ≥98% , CAS No.327031-55-0

CAS: 327031-55-0 Cat. No.: V414284 Summenformel: C17H15N7 Molekulargewicht: 317.35 EG-Nummer: 816-332-1 PubChem CID: 6410104
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QUALITÄT & REINHEIT ≥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
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Preis
Menge
5mg
V414284-5mg
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3 Auf Lager
78,01€
10mg
V414284-10mg
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3 Auf Lager
129,21€
25mg
V414284-25mg
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3 Auf Lager
257,63€
50mg
V414284-50mg
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2 Auf Lager
510,14€
100mg
V414284-100mg
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2 Auf Lager
836,41€
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Warum diese Qualität

≥98% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at -20°C,Argon charged Versand Ice chest + Ice pads. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 0 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

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 

Spezifikationen

Synonyme
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
Spezifikationen & Reinheit
≥98%
Biochemische und physiologische Mechanismen
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
Storage
Store at -20°C,Argon charged
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥98%
Produkteigenschaften
ALogP
3.589
HBD-Zahl
2
Rotationsfähige Bindung
3
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504764113
Kanonisches Lächeln
CC1=C2C(=CC=C1)C3=C(N2)N=C(N=N3)NN=C(C)C4=CC=CC=N4
IUPAC Name
6-methyl-N-[(E)-1-pyridin-2-ylethylideneamino]-5H-[1,2,4]triazino[5,6-b]indol-3-amine
InChIKey
UQOSBPRTQFFUOA-SRZZPIQSSA-N
INCHI
1S/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+
Isomere SMILES
CC1=C2C(=CC=C1)C3=C(N2)N=C(N=N3)N/N=C(\C)/C4=CC=CC=N4
PubChem CID
6410104
Molekulargewicht
317.35

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

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✅ Analysezertifikat (COA)

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🔬 Spezifikationsblatt

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
KlasseIndoles 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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (nicht menschlich)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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 TypeDatumArtikel
C2512114C2512114Certificate of AnalysisAug 12, 2022 V414284
K2215482K2215482Certificate of AnalysisAug 12, 2022 V414284
K2215483K2215483Certificate of AnalysisAug 12, 2022 V414284
K2215484K2215484Certificate of AnalysisAug 12, 2022 V414284
K2215485K2215485Certificate of AnalysisAug 12, 2022 V414284
K2215487K2215487Certificate of AnalysisAug 12, 2022 V414284
Chemische und physikalische Eigenschaften
LöslichkeitSolubility (25°C) In vitro DMSO: 13 mg/mL (40.96 mM); Water: ˂1 mg/mL Ethanol: ˂1 mg/mL
DMSO (mg/ml) Maximale Löslichkeit13
DMSO (mM) Maximale Löslichkeit40.9642350716874
Wasser (mg/ml) Maximale Löslichkeit˂1
Schmelzpunkt (°C)>264°C (dec.)
Molekulargewicht317.300 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
Lösungsrechner
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Häufig gestellte Fragen

What is the purity of this product?
This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at ?20 °C under argon. It is supplied under an argon blanket; reseal under inert gas after each use.
How is this product shipped?
This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 327031-55-0, the molecular formula is C17H15N7, and the molecular weight is 317.35 g/mol. InChIKey UQOSBPRTQFFUOA-SRZZPIQSSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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