Icariin

cas: 489-32-7 — see every product listed under this CAS number, including other names

Icariin (CAS 489-32-7) is a chemical reagent available from Chemat. Available pack sizes: on request, 100mg, 10mM (in 1ml dmso), 50mg, 2g, 1g, 5g, 25g. Offered by: Chemat Brand, GLPBio, Biosynth, Sigma-Aldrich.

brandChemat Brand
catalog numberULI080001
cas489-32-7
sizeon request
availability Do potwierdzenia przez Chemat|To be confirmed by Chemat
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Available pack sizes

brand size price
Chemat Brand on request price on request
GLPBio 100mg 625.12 Pln
GLPBio 10mM (in 1ml dmso) 536.19 Pln
GLPBio 50mg 540.87 Pln
Biosynth 2g price on request
Biosynth 1g price on request
Biosynth 5g price on request
Biosynth 25g price on request
Biosynth 10g price on request
Sigma-Aldrich 25MG 1351.00 Pln
HPC Standards 1x25mg price on request

properties

purityNo data
categoryChemicals
delivery timeTo be confirmed by Chemat
Structural formula: {0} (CAS {1})

Icariin is a member of the class of flavonols that is kaempferol which is substituted at position 8 by a 3-methylbut-2-en-1-yl group and in which the hydroxy groups at positions 3, 4', and 7 have been converted to the corresponding 6-deoxy-alpha-L-mannopyranoside, methyl ether, and beta-D-glucopyranoside, respectively. A phoshphodiesterase-5 inhibitor, it is obtained from several species of plants in the genus Epimedium and is thought to be the main active ingredient of the Chinese herbal medicine Herba Epimedii (yinyanghuo). It has a role as an antioxidant, a bone density conservation agent, an EC 3.1.4.35 (3',5'-cyclic-GMP phosphodiesterase) inhibitor and a phytoestrogen. It is a member of flavonols and a glycosyloxyflavone.

Source: ChEBI

Identity
Molecular formulaC33H40O15
Molecular weight676.7 g/mol
IUPAC name5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
InChIKeyTZJALUIVHRYQQB-XLRXWWTNSA-N
SMILESC[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O

Computed by PubChem (NCBI)

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