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Tracheloside - 98%, high purity , CAS No.33464-71-0

COA

Grade & Purity:

≥98%

Cas Number: 33464-71-0
Molecular Weight: 550.55
PubChem CID: 169511

In stock

Item Number

T412885

Grouped product items
SKU	Size	Availability	Price
T412885-1mg	1mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$54.90
T412885-5mg	5mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$116.90
T412885-25mg	25mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$526.90
T412885-100mg	100mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,895.90

phosphatase Inhibitors

View related series

Estrogen Receptor/ERR (213) Vitamin D Related/Nuclear Receptor (907)

Basic Description

Synonyms	MFCD00870631 \| s3284 \| DTXSID30955094 \| Tracheloside \| 2(3H)-FURANONE, 4-((3,4-DIMETHOXYPHENYL)METHYL)-3-((4-(.BETA.-D-GLUCOPYRANOSYLOXY)-3-METHOXYPHENYL)METHYL)DIHYDRO-3-HYDROXY-, (3S,4S)- \| CS-0017050 \| (3S,4S)-4-((3,4-DIMETHOXYPHENYL)METHYL)-3-((4-(.BE
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Tracheloside is a lignan glycoside isolated from seeds of Carthamus tinctorius with anti-estrogenic effects. Tracheloside significantly decreases the activity of alkaline phosphatase (AP) (an estrogen-inducible marker enzyme) with IC50 of 0.31 μg/ml. Trac
Storage Temp	Protected from light,Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Information Tracheloside Tracheloside is a lignan glycoside isolated from seeds of Carthamus tinctorius with anti-estrogenic effects. Tracheloside significantly decreases the activity of alkaline phosphatase (AP) (an estrogen-inducible marker enzyme) with IC50 of 0.31 μg/ml. Tracheloside promotes keratinocyte proliferation through ERK1/2 stimulation. Targets AP ; ERK

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lignans, neolignans and related compounds
  - Class Lignan glycosides

Kingdom	Organic compounds
Superclass	Lignans, neolignans and related compounds
Class	Lignan glycosides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Lignan glycosides
Alternative Parents	Dibenzylbutyrolactone lignans Lignan lactones Fatty acyl glycosides of mono- and disaccharides Phenolic glycosides Alkyl glycosides O-glycosyl compounds Dimethoxybenzenes Anisoles Phenoxy compounds Alkyl aryl ethers Oxanes Monosaccharides Gamma butyrolactones Tetrahydrofurans Tertiary alcohols Carboxylic acid esters Secondary alcohols Acetals Monocarboxylic acids and derivatives Oxacyclic compounds Polyols Carbonyl compounds Hydrocarbon derivatives Primary alcohols Organic oxides
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Lignan glycoside - Dibenzylbutyrolactone - Lignan lactone - Tetrahydrofuran lignan - 9,9p-epoxylignan - Furanoid lignan - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - O-dimethoxybenzene - Dimethoxybenzene - Phenoxy compound - Phenol ether - Methoxybenzene - Anisole - Alkyl aryl ether - Fatty acyl - Oxane - Monocyclic benzene moiety - Monosaccharide - Gamma butyrolactone - Benzenoid - Tetrahydrofuran - Tertiary alcohol - Secondary alcohol - Lactone - Carboxylic acid ester - Acetal - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Ether - Polyol - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxygen compound - Organic oxide - Primary alcohol - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.
External Descriptors	glycoside - lignan
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Product Properties

ALogP	0.949
HBD Count	4
Rotatable Bond	10

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	(3S,4S)-4-[(3,4-dimethoxyphenyl)methyl]-3-hydroxy-3-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one
INCHI	InChI=1S/C27H34O12/c1-34-17-6-4-14(9-19(17)35-2)8-16-13-37-26(32)27(16,33)11-15-5-7-18(20(10-15)36-3)38-25-24(31)23(30)22(29)21(12-28)39-25/h4-7,9-10,16,21-25,28-31,33H,8,11-13H2,1-3H3/t16-,21+,22+,23-,24+,25+,27-/m0/s1
InChIKey	LWYAMIUSVGPFKS-CGLYQLBNSA-N
Smiles	COC1=C(C=C(C=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC
Isomeric SMILES	COC1=C(C=C(C=C1)C[C@H]2COC(=O)[C@@]2(CC3=CC(=C(C=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)OC)O)OC
PubChem CID	169511
Molecular Weight	550.55

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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Analytical Chart:

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4 results found

Lot Number	Certificate Type	Date	Item
G2208392	Certificate of Analysis	Apr 07, 2025	T412885
G2208426	Certificate of Analysis	Apr 07, 2025	T412885
G2208434	Certificate of Analysis	Apr 07, 2025	T412885
G2208393	Certificate of Analysis	Apr 07, 2025	T412885

Chemical and Physical Properties

Solubility	Solubility (25°C) In vitro DMSO: 100 mg/mL (181.63 mM);
Sensitivity	Hygroscopic;Light sensitive
DMSO(mg / mL) Max Solubility	100
DMSO(mM) Max Solubility	181.636545272909
Water(mg / mL) Max Solubility	-1
Molecular Weight	550.600 g/mol
XLogP3	1.000
Hydrogen Bond Donor Count	5
Hydrogen Bond Acceptor Count	12
Rotatable Bond Count	10
Exact Mass	550.205 Da
Monoisotopic Mass	550.205 Da
Topological Polar Surface Area	174.000 Å²
Heavy Atom Count	39
Formal Charge	0
Complexity	799.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	7
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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