877-22-5 | 2-Hydroxy-3-methoxybenzoic acid

Packsize	Purity	Availability	Price	Discounted Price
10g	97%	in stock	$10.00	$7.00
100g	97%	in stock	$90.00	$63.00
500g	97%	in stock	$251.00	$176.00

Description

• Catalog Number: AB65260
• Chemical Name: 2-Hydroxy-3-methoxybenzoic acid
• CAS Number: 877-22-5
• Molecular Formula: C8H8O4
• Molecular Weight: 168.1467
• MDL Number: MFCD00002445
• SMILES: COc1cccc(c1O)C(=O)O

Computed Properties

• Complexity: 168
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• XLogP3: 1.9

Literature

• Photoinduced reactivity of doxorubicin: catalysis and degradation.

  The journal of physical chemistry. A 20120503

• Copper(II) complexes of salicylic acid combining superoxide dismutase mimetic properties with DNA binding and cleaving capabilities display promising chemotherapeutic potential with fast acting in vitro cytotoxicity against cisplatin sensitive and resistant cancer cell lines.

  Journal of medicinal chemistry 20120308

• 2-Hydr-oxy-3-methoxy-benzoic acid monohydrate.

  Acta crystallographica. Section E, Structure reports online 20080401

• Doxorubicin inhibits oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) by a lactoperoxidase/H(2)O(2) system by reacting with ABTS-derived radical.

  Archives of biochemistry and biophysics 20071015

• Inactivation of anthracyclines by serum heme proteins.

  Chemical research in toxicology 20070601

• Inactivation of anthracyclines by cellular peroxidase.

  Cancer research 20050715

• The enhancement of riboflavin-mediated photo-oxidation of doxorubicin by histidine and urocanic acid.

  Cancer chemotherapy and pharmacology 20010401