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Anthrarufin - ≥85.0%, high purity , CAS No.117-12-4

    Grade & Purity:
  • ≥85%
In stock
Item Number
A124340
Grouped product items
SKU Size
Availability
Price Qty
A124340-5g
5g
2
$9.90
A124340-10g
10g
3
$12.90
A124340-25g
25g
3
$23.90
A124340-100g
100g
3
$85.90
A124340-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$384.90

Basic Description

Synonyms NCI60_041483 | Anthrarufin | 1,5-Dihydroxy-9,10-anthraquinone | Epitope ID:116190 | InChI=1/C14H8O4/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6,15-16 | 9, 1,5-dihydroxy- | CCRIS 3150 | 1,5-Dihydroxyanthra-9,10-quinone # | 9,10-dihydroxy-1,5-a
Specifications & Purity ≥85%
Storage Temp Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Anthracenes
Subclass Anthraquinones
Intermediate Tree Nodes Not available
Direct Parent Anthraquinones
Alternative Parents Aryl ketones  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Vinylogous acids  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homopolycyclic compounds
Substituents Anthraquinone - 9,10-anthraquinone - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Vinylogous acid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.
External Descriptors dihydroxyanthraquinone

Associated Targets(Human)

MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A498 (42825 Activities)
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ACHN (49357 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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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 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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Raji (5516 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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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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SNB-78 (14240 Activities)
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TK-10 (45540 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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786-0 (47912 Activities)
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A549 (127892 Activities)
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EKVX (44102 Activities)
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A-431 (6446 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-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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LOX IMVI (44321 Activities)
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HOP-62 (47048 Activities)
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LXFL 529 (14112 Activities)
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M19-MEL (15326 Activities)
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SNB-75 (44215 Activities)
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NCI-H226 (44470 Activities)
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NCI-H23 (49055 Activities)
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Associated Targets(non-human)

Ttr Transthyretin (14 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
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Trichoplusia ni (986 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

Pubchem Sid 504751647
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504751647
IUPAC Name 1,5-dihydroxyanthracene-9,10-dione
INCHI InChI=1S/C14H8O4/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6,15-16H
InChIKey JPICKYUTICNNNJ-UHFFFAOYSA-N
Smiles C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)O
Isomeric SMILES C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)O
RTECS CB6630000
Molecular Weight 240.21
Beilstein 1881718
Reaxy-Rn 1881718
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1881718&ln=

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

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.

11 results found

Lot Number Certificate Type Date Item
G2121131 Certificate of Analysis May 07, 2025 A124340
G2121132 Certificate of Analysis May 07, 2025 A124340
H2304073 Certificate of Analysis Jun 07, 2023 A124340
H2304072 Certificate of Analysis Jun 07, 2023 A124340
H2304070 Certificate of Analysis Jun 07, 2023 A124340
H2304077 Certificate of Analysis Jun 07, 2023 A124340
H2304085 Certificate of Analysis Jun 07, 2023 A124340
H2304078 Certificate of Analysis Jun 07, 2023 A124340
H2304076 Certificate of Analysis Jun 07, 2023 A124340
H2304086 Certificate of Analysis Jun 07, 2023 A124340
H2304079 Certificate of Analysis Jun 07, 2023 A124340

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Chemical and Physical Properties

Solubility Solubility in water: Practically insoluble; Soluble in Alcohol,Ether,Benzene
Melt Point(°C) 279 °C
Molecular Weight 240.210 g/mol
XLogP3 3.700
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 0
Exact Mass 240.042 Da
Monoisotopic Mass 240.042 Da
Topological Polar Surface Area 74.600 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 342.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
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

Citations of This Product

1. Dong Lu, Ke Lu, Hong-Tao Wen, Zhan Wei, Alberto Bianco, Gui-Gen Wang, Hua-Yu Zhang.  (2023)  Synthesis of Visible Light Excitable Carbon Dot Phosphor-Al2O3 Hybrids for Anti-Counterfeiting and Information Encryption.  Small,  19  (31): (2207046). 
2. Yuanyuan Song, Ziqi Wang, Yijing Long, Yang Mao, Feng Jiang, Yuanyuan Lu.  (2022)  2-Alkyl-anthraquinones inhibit Candida albicans biofilm via inhibiting the formation of matrix and hyphae.  RESEARCH IN MICROBIOLOGY,  173  (103955). 

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