Tiliroside

CAT: 0931-T5S1172-01Size: 2 mgDry Ice: NoHazardous: No

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CAT#:0931-T5S1172-01Size:2 mg

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CAS Number

20316-62-5

Target

Antioxidant

Related Pathways

Oxidation-Reduction

Purity

0.9981

Bioactivity

1. Tiliroside (Tribuloside) shows anticarcinogenic activity. 2. Tiliroside shows hepatoprotective activity. 3. Tiliroside shows antioxidant and anti-inflammatory activity, can inhibit neuroinflammation in neurodegenerative disorders. 4. Tiliroside has anti-diabetic effect, are at least partially mediated through inhibitory effects on carbohydrate digestion and glucose uptake in the gastrointestinal tract. 5. Tiliroside and gnaphaliin are antioxidants against in vitro Cu (2+) -induced LDL oxidation in the same order of magnitude compared to that of the reference drug, probucol. 6. Tiliroside enhances fatty acid oxidation via the enhancement adiponectin signaling associated with the activation of both AMP-activated protein kinase and peroxisome proliferator-activated receptor α and ameliorates obesity-induced metabolic disorders.

Smiles

OC1C(COC(=O)C=Cc2ccc(O)cc2)OC(Oc2c(oc3cc(O)cc(O)c3c2=O)-c2ccc(O)cc2)C(O)C1O

Molecular Formula

C30H26O13

Molecular Weight

594.52

Shipping Conditions

Ice Packs

Storage Temperature

-20°C

Chemical Information

Tiliroside

Tribuloside is a glycosyloxyflavone that is kaempferol attached to a 6-O-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has a role as a plant metabolite. It is a trihydroxyflavone, a cinnamate ester, a glycosyloxyflavone and a monosaccharide derivative. It is functionally related to a kaempferol and a trans-4-coumaric acid.

CAS Number	20316-62-5
PubChem CID	5320686
IUPAC Name	[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate
Molecular Formula	C30H26O13
Molecular Weight	594.5
XLogP	2.5
Topological Polar Surface Area	213
Hydrogen Bond Donor Count	7
Hydrogen Bond Acceptor Count	13
Rotatable Bond Count	8
Heavy Atom Count	43
Formal Charge	0
Complexity	1040

SMILES

C1=CC(=CC=C1/C=C/C(=O)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O

InChI

InChI=1S/C30H26O13/c31-16-6-1-14(2-7-16)3-10-22(35)40-13-21-24(36)26(38)27(39)30(42-21)43-29-25(37)23-19(34)11-18(33)12-20(23)41-28(29)15-4-8-17(32)9-5-15/h1-12,21,24,26-27,30-34,36,38-39H,13H2/b10-3+/t21-,24-,26+,27-,30+/m1/s1

InChIKey

DVGGLGXQSFURLP-VWMSDXGPSA-N

Chemical Structure

2D Structure

CAS: 20316-62-5

CID: 5320686

Formula: C30H26O13

MW: 594.5

Interactive 3D Structure

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View on PubChem Raw 3D data

Computed Properties

Property	Value
Molecular Weight	594.5
XLogP3	2.5
Hydrogen Bond Donor Count	7
Hydrogen Bond Acceptor Count	13
Rotatable Bond Count	8
Exact Mass	594.13734088
Monoisotopic Mass	594.13734088
Topological Polar Surface Area	213 Å²
Heavy Atom Count	43
Formal Charge	0
Complexity	1040
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
Covalently-Bonded Unit Count	1
Compound Is Canonicalized	Yes

Alternative Products

Catalog	Name
N2081-20	Tiliroside
A12131-100	Tiliroside 100mg
HY-126422-01	Cis-Tiliroside
A12131-10	Tiliroside 10mg
A12131-5	Tiliroside 5mg

Tiliroside

Chemical Information

Alternative Products

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