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9,10-Anthracenedicarboxylic acid (H2L) is an anthracene based dicarboxylic compound, which has a larger conjugating π-system that enables the development of fluorescent materials. It has interesting magnetic and luminescent properties. It can be used as a bridging carboxylic acid ligand with a steric bulk due to the presence of its anthracene ring. Group: Carboxylic acid mof ligand-dicarboxylic acid mof ligand. Alternative Names: H2ADC. CAS No. 73016-08-7. Product ID: anthracene-9,10-dicarboxylic acid. Molecular formula: 266.25. Mole weight: C16H10O4. C1=CC=C2C (=C1)C (=C3C=CC=CC3=C2C (=O)O)C (=O)O. 1S/C16H10O4/c17-15 (18)13-9-5-1-2-6-10 (9)14 (16 (19)20)12-8-4-3-7-11 (12)13/h1-8H, (H, 17, 18) (H, 19, 20). FDFGHPKPHFUHBP-UHFFFAOYSA-N. 96%.
9-Anthracenecarboxylic Acid
9-Anthracenecarboxylic Acid. Group: Small molecule semiconductor building blocks. CAS No. 723-62-6. Product ID: anthracene-9-carboxylic acid. Molecular formula: 222.24g/mol. Mole weight: C15H10O2. C1=CC=C2C(=C1)C=C3C=CC=CC3=C2C(=O)O. InChI=1S/C15H10O2/c16-15 (17)14-12-7-3-1-5-10 (12)9-11-6-2-4-8-13 (11)14/h1-9H, (H, 16, 17). XGWFJBFNAQHLEF-UHFFFAOYSA-N.
9-Anthracenecarboxylic acid ethyl ester
9-Anthracenecarboxylic acid ethyl ester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 9-Anthracenecarboxylic acid ethyl ester, 1754-54-7, ethyl anthracene-9-carboxylate, CTK0E3911, SBB068577, ZINC39258768, AKOS015838808, AG-L-22312, 9-Anthracenecarboxylic acid, ethyl ester, FT-0655281, A812088, I14-7485. Product Category: Heterocyclic Organic Compound. CAS No. 1754-54-7. Molecular formula: C17H14O2. Mole weight: 250.291860 [g/mol]. Purity: 0.96. IUPACName: ethyl anthracene-9-carboxylate. Canonical SMILES: CCOC(=O)C1=C2C=CC=CC2=CC3=CC=CC=C31. Density: 1.18g/cm³. Product ID: ACM1754547. Alfa Chemistry ISO 9001:2015 Certified.
9-Anthracenecarboxylic acid methyl ester
9-Anthracenecarboxylic acid methyl ester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 9-Methoxycarbonylanthracene, 1504-39-8, 9-Anthracenecarboxylic acid methyl ester, Methyl 9-anthracenecarboxylate, 9-Anthracenecarboxylic acid, methyl ester, 9-Anthroic acid, methyl ester, Methyl 9-anthroate, AC1Q5ZJA, AC1L40IA, methyl anthracene-9-carboxylate, SCHEMBL10559440, CTK4C6642, MolPort-001-860-136, AR-1H5852, NSC176183, SBB068576, ZINC00400397, AKOS015852095, MCULE-1474817814, NSC-176183. Product Category: Heterocyclic Organic Compound. CAS No. 1504-39-8. Molecular formula: C16H12O2. Mole weight: 236.265280 [g/mol]. Purity: 0.96. IUPACName: methyl anthracene-9-carboxylate. Canonical SMILES: COC(=O)C1=C2C=CC=CC2=CC3=CC=CC=C31. Density: 1.208g/cm³. Product ID: ACM1504398. Alfa Chemistry ISO 9001:2015 Certified.
9-Anthracenecarboxylic Acid (purified by sublimation)
9-Anthracenecarboxylic Acid (purified by sublimation). Group: other material building blocks. CAS No. 723-62-6. Product ID: anthracene-9-carboxylic acid. Molecular formula: 222.24g/mol. Mole weight: C15H10O2. C1=CC=C2C(=C1)C=C3C=CC=CC3=C2C(=O)O. InChI=1S/C15H10O2/c16-15 (17)14-12-7-3-1-5-10 (12)9-11-6-2-4-8-13 (11)14/h1-9H, (H, 16, 17). XGWFJBFNAQHLEF-UHFFFAOYSA-N.
Anthracene-2-carboxylic acid
Anthracene-2-carboxylic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 613-08-1. Pack Sizes:5g, 1g, 2g. US Biological Life Sciences.
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Anthracene-9-carboxylic acid
Anthracene-9-carboxylic acid (9-Anthracenecarboxylic acid) is an anthracene derivative traditionally used to block and identify Ca 2+ -activated Cl - currents (CaCCs) in various cell types, like diverse smooth muscle cells, epithelial cells and salivary gland cells [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 9-Anthracenecarboxylic acid. CAS No. 723-62-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-101329.
Anthracene-9-carboxylic acid-d9
Anthracene-9-carboxylic acid-d 9 is the deuterium labeled Anthracene-9-carboxylic acid[1]. Anthracene-9-carboxylic acid (9-Anthracenecarboxylic acid) is an anthracene derivative traditionally used to block and identify Ca2+-activated Cl- currents (CaCCs) in various cell types, like diverse smooth muscle cells, epithelial cells and salivary gland cells[2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: 9-Anthracenecarboxylic acid-d9. CAS No. 1219803-78-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-101329S.
3-Chloroanthraquinone-2-carboxylic acid
3-Chloroanthraquinone-2-carboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-CHLOROANTHRAQUINONE-3-CARBOXYLIC ACID;3-CHLOROANTHRAQUINONE-2-CARBOXYLIC ACID;3-CHLORO-9 10-DIHYDRO-9 10-DIOXO-2-ANTHROIC ACID;3-chloro-9,10-dihydro-9,10-dioxoanthracene-2-carboxylic acid;3-Chloro-9,10-dihydro-9,10-dioxo-2-anthracenecarboxylic acid;3-c. Product Category: Heterocyclic Organic Compound. CAS No. 84-32-2. Molecular formula: C15H7ClO4. Mole weight: 286.67. Purity: 0.96. IUPACName: 3-chloro-9,10-dioxoanthracene-2-carboxylic acid. Canonical SMILES: C1=CC=C2C(=C1)C(=O)C3=CC(=C(C=C3C2=O)Cl)C(=O)O. Density: 1.561g/cm³. ECNumber: 201-526-5. Product ID: ACM84322. Alfa Chemistry ISO 9001:2015 Certified.
4-Acetyl Rhein
4-Acetyl Rhein. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4-Acetoxy-5-hydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic Acid, 4-Acetyl Rhein, Monoacetyl Rhein Isomer B,2-Anthracenecarboxylic acid, 4-(acetyloxy)-9,10-dihydro-5-hydroxy-9,10-dioxo-. CAS No. 875535-36-7. IUPAC Name: 4-acetyloxy-5-hydroxy-9,10-dioxoanthracene-2-carboxylic acid. Molecular Formula: C17H10O7. Mole Weight: 326.26. Catalog: APS875535367. SMILES: CC (=O)Oc1cc (cc2C (=O)c3cccc (O)c3C (=O)c12)C (=O)O. Format: Neat.
A diacetyl derivative of Rhein. Demonstrates anti-arthritic activity without inhibiting prostaglandin synthesis. Antiarthritic. Group: Biochemicals. Alternative Names: 4,5-Bis(acetyloxy)-9,10-dihydro-9,10-dioxo-2-anthracenecarboxylic Acid; 4,5-Diacetoxyanthraquinone-2-carboxylic Acid; 4,5-Diacetylrhein; Artrodar; DAR; Diacerhein; Diacetylrhein; Fisiodar; SF 277. Grades: Highly Purified. CAS No. 13739-02-1. Pack Sizes: 100mg. US Biological Life Sciences.
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Diacerein-13C6
A diacetyl derivative of Rhein. Demonstrates anti-arthritic activity without inhibiting prostaglandin synthesis. Antiarthritic. Group: Biochemicals. Alternative Names: 4,5-Bis(acetyloxy)-9,10-dihydro-9,10-dioxo-2-anthracenecarboxylic Acid-13C6; 4,5-Diacetoxyanthraquinone-2-carboxylic Acid-13C6; 4,5-Diacetylrhein-d5; Artrodar-13C6; DAR-13C6; Diacerhein-13C6; Diacetylrhein-13C6; Fisiodar-13C6. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Gallocyanine
Gallocyanine belongs to the oxazine class of dyes and is often used to stain animal cells, mostly the nucleic acids. Gallocyanine is known to inhibit Dickkopf-1 (Dkk1), an antagonist of the Wnt pathway. Synonyms: IIIC3; Alizarine Navy Blue; Anthracene Blue SWGG; Brilliant Chrome Blue P; C.I. 51030; Fast Violet; Mordant Blue 10; 7-Dimethylamino-4-hydroxy-3-oxo-phenoxazine-1-carboxylic acid. Grades: ≥95%. CAS No. 1562-85-2. Molecular formula: C15H13N2O5·Cl. Mole weight: 336.7.
Found in the free state and as glucoside in Rheum spp, Polygonaceae (rhubarb) and in Senna leaves. A potential antioxidant resource: endophytic fungi from medicinal plants. Group: Biochemicals. Alternative Names: 9,10-Dihydro-4,5-dihydroxy-9,10-dioxo-2-anthracenecarboxylic Acid; 4, 5-Di hydroxy-2-anthraquinonecarboxyl ic Acid; Chrysazin-3-carboxylic Acid; Monorhein; NSC 38629; Rheic Acid; Rhubarb Yellow. Grades: Highly Purified. CAS No. 478-43-3. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
Rhein-13C6
Found in the free state and as glucoside in Rheum spp, Polygonaceae (rhubarb) and in Senna leaves. A potential antioxidant resource: endophytic fungi from medicinal plants. Group: Biochemicals. Alternative Names: 9,10-Dihydro-4,5-dihydroxy-9,10-dioxo-2-anthracenecarboxylic Acid-13C6 ; 4, 5-Di hydroxy-2-anthraquinonecarboxyl ic Acid-13C6 ; Chrysazin-3-carboxylic Acid-13C6 ; Monorhein-13C6 ; NSC 38629-13C6; Rheic Acid-13C6 ; Rhubarb Yellow-13C6. Grades: Highly Purified. CAS No. 1330166-42-1. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Sennidin A
Sennidin A, isolated from the leaves of Cassia angustifolia, inhibits HCV NS3 helicase, with an IC50 of 0.8 μM. Sennidin A induces phosphorylation of Akt and glucose transporter 4 (GLUT4) translocation. Sennidin A stimulates the glucose incorporation. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (9R, 9'R) - Rel- (+) -9, 9', 10, 10'- Tetrahydro- 4, 4', 5, 5'- tetrahydroxy- 10, 10'- dioxo- [9, 9'- Bianthracene] - 2, 2'- dicarboxylic acid. Product Category: Inhibitors. Appearance: Solid. CAS No. 641-12-3. Molecular formula: C30H18O10. Mole weight: 538.46. Purity: 0.98. IUPACName: 9-(2-carboxy-4,5-dihydroxy-10-oxo-9H-anthracen-9-yl)-4,5-dihydroxy-10-oxo-9H-anthracene-2-carboxylic acid. Canonical SMILES: C1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)C(=O)O)C=C(C=C3O)C(=O)O. Product ID: ACM641123-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Senni (disambiguation).
Sennidin B
Sennidin B, a stereoisomer isolated from the leaves of Cassia angustifolia, has lower activity than Sennidin A. Sennidin A inhibits HCV NS3 helicase, with an IC50 of 0.8 μM. Sennidin A induces phosphorylation of Akt and glucose transporter 4 (GLUT4) translocation. Sennidin A stimulates the glucose incorporation. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 9-(2-Carboxy-4,5-dihydroxy-10-oxo-9H-anthracen-9-yl)-4,5-dihydroxy-10-oxo-9H-anthracene-2-carboxylic acid. Product Category: Inhibitors. Appearance: Powder. CAS No. 517-44-2. Molecular formula: C30H18O10. Mole weight: 538.46. Purity: 0.98. IUPACName: (9S)-9-[(9R)-2-carboxy-4,5-dihydroxy-10-oxo-9H-anthracen-9-yl]-4,5-dihydroxy-10-oxo-9H-anthracene-2-carboxylic acid. Canonical SMILES: C1=CC2=C(C(=C1)O)C(=O)C3=C([C@@H]2[C@H]4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)C(=O)O)C=C(C=C3O)C(=O)O. Density: 1.695±0.06 g/ml. Product ID: ACM517442. Alfa Chemistry ISO 9001:2015 Certified.
Sennoside A
Sennoside A is an anthraquinone glycoside, found in Senna (Cassia angustifolia). Sennoside A is a HIV-1 inhibitor effective on HIV-1 replication. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4,4',10,10'-Tetrahydroxy-5,5'-bis(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-[9,9'-bianthracene]-2,2'-dicarboxylic acid. Product Category: Inhibitors. Appearance: Yellow solid. CAS No. 81-27-6. Molecular formula: C42H38O20. Mole weight: 862.75. Purity: 0.98. IUPACName: (9R)-9-[(9R)-2-carboxy-4-hydroxy-10-oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9H-anthracen-9-yl]-4-hydroxy-10-oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9H-anthracene-2-carboxylic acid. Canonical SMILES: C1=CC2=C(C(=C1)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C(=O)C4=C([C@@H]2[C@@H]5C6=C(C(=CC=C6)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)C(=O)O. Density: 1.743±0.06 g/ml. Product ID: ACM81276-1. Alfa Chemistry ISO 9001:2015 Certified.
Dioxamycin
It is produced by the strain of Streptomyces xantholiticus. It has anti-gram-positive bacterial activity. It can inhibit Staphylococcus aureus 209P with MIC of 3.12 μg/mL. It inhibits the growth of L1210, P388, IMC, LX-1 and SC-6 cells with IC50 (μg/mL) of 2.7, 1.4, 6.0, 2.0 and 2.5, respectively. Synonyms: 1,3-Dioxolane-2-carboxylic acid, 2,4-dimethyl-5-(7-oxo-7-((tetrahydro-2-methyl-6-(1,2,3,4,4a,7,12,12b-octahydro-2,3,4a,8,12b-pentahydroxy-3-methyl-1,7,12-trioxobenz(a)anthracen-9-yl)-2H-pyran-3-yl)oxy)-1,3,5-heptatrienyl)-, (2-alpha,3-alpha,4a-alpha, 9(2R*, 3S*(1E(2S*, 4S*, 5S*), 3E, 5E)6R*), 12b-alpha)-(+)-. Grades: >95%. CAS No. 134861-62-4. Molecular formula: C38H40O15. Mole weight: 736.72.
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