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Austdiol - ≥95% (LC/MS-ELSD), high purity , CAS No.53043-28-0

    Grade & Purity:
  • ≥95%(LC/MS-ELSD)
In stock
Item Number
A463846
Grouped product items
SKU Size
Availability
Price Qty
A463846-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$889.90

Basic Description

Synonyms BRN 1383761 | DTXSID70201087 | NCI60_001176 | AKOS040734783 | (7R,8S)-7,8-Dihydro-7,8-dihydroxy-3,7-dimethyl-6-oxo-6H-2-benzopyran-5-carbaldehyde | CHEBI:174211 | 6H-2-Benzopyran-5-carboxaldehyde,8-dihydro-7,8-dihydroxy-3,7-dimethyl-6-oxo-, (7R-trans)- |
Specifications & Purity ≥95%(LC/MS-ELSD)
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Description

Natural product derived from fungal source.}

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Azaphilones
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Azaphilones
Alternative Parents Cyclohexenones  Pyrans  Acyloins  Tertiary alcohols  Secondary alcohols  1,2-diols  Oxacyclic compounds  Organic oxides  Hydrocarbon derivatives  Aldehydes  
Molecular Framework Aliphatic heteropolycyclic compounds
Substituents Azaphilone - Cyclohexenone - Acyloin - Pyran - Tertiary alcohol - 1,2-diol - Ketone - Cyclic ketone - Secondary alcohol - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Aldehyde - Alcohol - Organic oxide - Organic oxygen compound - Aliphatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as azaphilones. These are a structurally variable family of fungal polyketide metabolites possessing a highly oxygenated pyranoquinone bicyclic core, usually known as isochromene, and a quaternary carbon center.
External Descriptors Not available

Associated Targets(Human)

A498 (42825 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DLD-1 (17511 Activities)
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DMS-273 (14108 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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SNB-78 (14240 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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XF498 (12972 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HOP-18 (11577 Activities)
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HOP-92 (41141 Activities)
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NCI-H460 (60772 Activities)
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SF-268 (49410 Activities)
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IGROV-1 (47897 Activities)
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KM-20L2 (14967 Activities)
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LOX IMVI (44321 Activities)
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HOP-62 (47048 Activities)
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M19-MEL (15326 Activities)
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MDA-MB-435 (38290 Activities)
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Malme-3M (44254 Activities)
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SNB-75 (44215 Activities)
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Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)
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Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
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Acinetobacter baumannii (41033 Activities)
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Escherichia coli (133304 Activities)
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Cryptococcus neoformans (21258 Activities)
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Candida albicans (78123 Activities)
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Leishmania donovani (89745 Activities)
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Leishmania major (2877 Activities)
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P388 (20296 Activities)
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P388/ADR (1216 Activities)
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Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (7R,8S)-7,8-dihydroxy-3,7-dimethyl-6-oxo-8H-isochromene-5-carbaldehyde
INCHI InChI=1S/C12H12O5/c1-6-3-7-8(4-13)10(14)12(2,16)11(15)9(7)5-17-6/h3-5,11,15-16H,1-2H3/t11-,12-/m0/s1
InChIKey QVMUHZHZYCDMAI-RYUDHWBXSA-N
Smiles CC1=CC2=C(C(=O)C(C(C2=CO1)O)(C)O)C=O
Isomeric SMILES CC1=CC2=C(C(=O)[C@]([C@H](C2=CO1)O)(C)O)C=O
UN Number 2811
Molecular Weight 236.22
Reaxy-Rn 20406774
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20406774&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Flash Point(°F) Not applicable
Flash Point(°C) Not applicable
Molecular Weight 236.220 g/mol
XLogP3 -1.200
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 1
Exact Mass 236.068 Da
Monoisotopic Mass 236.068 Da
Topological Polar Surface Area 83.800 Ų
Heavy Atom Count 17
Formal Charge 0
Complexity 497.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 2
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

Solution Calculators

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