ChemicalBook--->CAS DataBase List--->117570-53-3

117570-53-3

117570-53-3 Structure

117570-53-3 Structure
IdentificationBack Directory
[Name]

5,6-Dimethylxantheonone-4-acetic acid
[CAS]

117570-53-3
[Synonyms]

DMXAA
DMAXX
CS-1975
ASA-404
vadimezan
NSC-640488
NSC-649488
DMXAA, >=99%
DMXAA(ASA404)
DMXAA Vadimezan
DMXAA(AS1404,ASA404)
DMXAA (ASA404,Vadimezan)
VadiMezan(DMXAA,NSC 640488)
5,6-dimethylxanthenoneacetic acid
5,6-Dimethylxanthenone-4-acetic acid
5,6-Dimethylxantheonone-4-acetic acid
(5,6-DIMETHYL-9-OXO-XANTHEN)-4-ACETIC ACID
5,6-Dimethyl-9-oxo-9H-xanthene-4-acetic acid
9H-Xanthene-4-aceticacid, 5,6-dimethyl-9-oxo-
2-(5,6-Dimethyl-9-oxoxanthen-4-yl)acetic Acid
5,6-Dimethylxantheonone-4-acetic acid USP/EP/BP
5,6-Dimethylxantheonone-4-acetic acid(DMXAA) ,98%
5,6-DiMethyl-9-oxo-9H-xanthene-4-acetic acid DMXAA, ASA404
DMXAA,5,6-Dimethylxanthenone-4-acetic Acid, ASA404, Vadimezan
[EINECS(EC#)]

700-141-4
[Molecular Formula]

C17H14O4
[MDL Number]

MFCD00870555
[MOL File]

117570-53-3.mol
[Molecular Weight]

282.29
Chemical PropertiesBack Directory
[Melting point ]

259-261 °C
[Boiling point ]

520.9±50.0 °C(Predicted)
[density ]

1.321±0.06 g/cm3(Predicted)
[vapor pressure ]

0Pa at 20℃
[storage temp. ]

2-8°C
[solubility ]

DMSO: 17 mg/mL, soluble
[form ]

solid
[pka]

4.21±0.10(Predicted)
[color ]

light brown
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in DMSO or DMF may be stored at -20°C for up to 3 months.
[InChI]

InChI=1S/C17H14O4/c1-9-6-7-13-15(20)12-5-3-4-11(8-14(18)19)17(12)21-16(13)10(9)2/h3-7H,8H2,1-2H3,(H,18,19)
[InChIKey]

XGOYIMQSIKSOBS-UHFFFAOYSA-N
[SMILES]

C1(=O)C2=C(C(C)=C(C)C=C2)OC2=C1C=CC=C2CC(O)=O
Safety DataBack Directory
[Hazard Codes ]

Xn,N
[Risk Statements ]

22-50/53
[Safety Statements ]

60-61
[RIDADR ]

UN 3077 9/PG 3
[WGK Germany ]

3
[RTECS ]

ZD5536200
[HS Code ]

2932.99.7000
[REACH Registrations]

Inactive
[HazardClass ]

9
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Aquatic Acute 1
Raw materials And Preparation ProductsBack Directory
Hazard InformationBack Directory
[Description]

DMXAA (117570-53-3) is a STING (Stimulator of Interferon Genes) agonist selective for mouse STING.1,2 Intratumoral administration of DMXAA resulted in tumor regression and complete rejection in mouse xenografts.3 Tumor regression induced by DMXAA results from a cascade of cellular events which include disruption of tumor vasculature followed by the release of chemokines which trigger the recruitment of immune cells.4 DMXAA induced expression of IFN-β resulting in a striking expansion of leukemia-specific T cells extending survival in two acute myeloid leukemia models.5
[Uses]

Vadimezan is a drug that displayed vascular-disrupting activity and induced haemorrhagic necrosis and tumour regression in pre-clinical animal models.
[Definition]

ChEBI: A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens is replaced by a 5,6-dimethyl-9-oxoxanthen-4-yl group.
[General Description]

5,6-dimethylxanthenone-4-acetic acid (DMXAA) is a flavone acetic acid derivative. It acts as a vascular disrupting agent (VDA), which damages tumor vasculature and stimulates an anti-tumor immune response. It stimulates hemorrhagic necrosis.
[Biochem/physiol Actions]

DMXAA is an apoptosis inducer; anti-vascular.
[storage]

Store at +4°C
[References]

1) Prantner et al. (2012), 5,6-Dimethylzanthenone-4-acetic acid (DMXAA) activates stimulator of interferon gene (STING)-dependent innate immune pathways and is regulated by mitochondrial membrane potential; J. Biol. Chem., 287 39776 2) Conlon et al. (2013), Mouse, but not human STING, binds and signals in response to the vascular disrupting agent 5,6-dimethylxanthenone-4-acetic acid; J. Immunol., 190 5216 3) Corrales et al. (2015), Direct Activation of STING in the Tumor Microenvironment Leads to Potent and Systemic Tumor Regression and immunity; Cell Rep., 11 1018 4) Weiss et al. (2017), The STING agonist DMXAA triggers a cooperation between T lymphocytes and myeloid cells that leads to tumor regression; Oncoimmunology, 6 e1346765 5) Curran et al. (2016), STING Pathway Activation Stimulates Potent Immunity Against Acute Myeloid Leukemia; Cell Rep., 15 2357
Spectrum DetailBack Directory
[Spectrum Detail]

Vadimezan(117570-53-3)MS
Vadimezan(117570-53-3)1HNMR
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