282200

Galangin

autophagy inducing flavonoid

Manufacturer: Sigma Aldrich

CAS Number: 548-83-4

Synonym(S): 3,5,7-Trihydroxyflavone, Norizalpinin

Select a Size

Pack Size SKU Availability Price
25 MG 282200-25-MG In Stock ₹ 9,341.98
100 MG 282200-100-MG In Stock ₹ 22,375.28

282200 - 25 MG

₹ 9,341.98

In Stock

Quantity

1

Base Price: ₹ 9,341.98

GST (18%): ₹ 1,681.556

Total Price: ₹ 11,023.536

Quality Level

100

Assay

≥95% (HPLC)

form

powder

color

yellow

mp

214-215 °C (lit.)

SMILES string

Oc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3ccccc3

InChI

1S/C15H10O5/c16-9-6-10(17)12-11(7-9)20-15(14(19)13(12)18)8-4-2-1-3-5-8/h1-7,16-17,19H

InChI key

VCCRNZQBSJXYJD-UHFFFAOYSA-N

Gene Information

human ... ADORA2A(135) , ADORA3(140) , CYP1A2(1544) rat ... Adora1(29290) , Adora2a(25369)

Other Options

Image Product Name Manufacturer Price Range
11-100-1998
Galangin, ≥97% (HPLC), MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 25,668.00
50-218-3991
eMolecules​ Galangin | 548-83-4 | MFCD00006833 | 1g
eMolecules​ ₹ 35,264.41
92342
Galangin
Supelco ₹ 26,283.10
PHL89505
Galangin
Sigma Aldrich ₹ 34,066.28
282200
Galangin
Sigma Aldrich ₹ 9,341.98 - ₹ 22,375.28

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Description

  • General description: Galangin is a flavonoid isolated from members of the Zingiberaceae family, which are mainly used for herbal medicines.[1]
  • Application: Galangin has been used: as a test drug to test its ameliorative effect in a rodent model of cisplatin-induced nephrotoxicity[1]to test its effect on the differentiation of 3T3-L1 preadipocyte cells into adipocytes[2]as an internal standard in nuclear magnetic resonance spectroscopy and mass spectroscopy[3]
  • Biochem/physiol Actions: Galangin exhibits antioxidant, anti-apoptotic, anti-inflammatory[1] and anti-obesity properties.[4] In addition, it also possesses anti-genotoxic activity against environmental and dietary carcinogens. Galangin inhibits cancer growth by hindering cancer cell proliferation, induction of apoptosis and autophagy and inhibition of metastasis.[5] Galangin also has an ability to inhibit CYP1A1 (Cytochrome P450, family 1, member A1) activity.[6]

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Show Difference

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Sigma Aldrich

282200

autophagy inducing flavonoid...


Quality Level:
100

Assay:
≥95% (HPLC)

form:
powder

color:
yellow

mp:
214-215 °C (lit.)

SMILES string:
Oc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3ccccc3

InChI:
1S/C15H10O5/c16-9-6-10(17)12-11(7-9)20-15(14(19)13(12)18)8-4-2-1-3-5-8/h1-7,16-17,19H

InChI key:
VCCRNZQBSJXYJD-UHFFFAOYSA-N

Gene Information:
human ... ADORA2A(135) , ADORA3(140) , CYP1A2(1544) rat ... Adora1(29290) , Adora2a(25369)

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form:
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white to off-white

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SMILES string:
[Na+].Cc1onc(-c2ccccc2)c1C(=O)N[C@H]3C4SC(C)(C)[C@@H](N4C3=O)C([O-])=O

InChI:
1S/C19H19N3O5S.Na/c1-9-11(12(21-27-9)10-7-5-4-6-8-10)15(23)20-13-16(24)22-14(18(25)26)19(2,3)28-17(13)22;/h4-8,13-14,17H,1-3H3,(H,20,23)(H,25,26);/q;+1/p-1/t13-,14+,17?;/m1./s1

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SMILES string:
[Na+].Cc1onc(-c2ccccc2)c1C(=O)N[C@H]3C4SC(C)(C)[C@@H](N4C3=O)C([O-])=O

InChI:
1S/C19H19N3O5S.Na/c1-9-11(12(21-27-9)10-7-5-4-6-8-10)15(23)20-13-16(24)22-14(18(25)26)19(2,3)28-17(13)22;/h4-8,13-14,17H,1-3H3,(H,20,23)(H,25,26);/q;+1/p-1/t13-,14+,17?;/m1./s1

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Gene Information:
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Supelco

28221-U

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__

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form:
__

color:
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__

InChI:
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InChI key:
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