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Lobetyolin - 99%, high purity , CAS No.129277-38-9

COA

Grade & Purity:

≥98%

Cas Number: 136085-37-5
Molecular Weight: 396.43
PubChem CID: 53486204

In stock

Item Number

L648060

Grouped product items
SKU	Size	Availability	Price
L648060-1mg	1mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$47.90
L648060-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$150.90
L648060-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$166.90
L648060-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$249.90
L648060-50mg	50mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$399.90

View related series

Metabolic Enzyme/Protease (4860) Xanthine Oxidase (24)

Basic Description

Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Lobetyolin, a bioactive compound, is derived from Codonopsis pilosula . Lobetyolin has anti-inflammatory, anti-oxidative and xanthine oxidase inhibiting activities. Lobetyolin also induces the apoptosis via the inhibition of ASCT2 -mediated glutamine meta
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	Lobetyolin, a bioactive compound, is derived from Codonopsis pilosula. Lobetyolin has anti-inflammatory, anti-oxidative and xanthine oxidase inhibiting activities. Lobetyolin also induces the apoptosis via the inhibition of ASCT2-mediated glutamine metabolism. Lobetyolin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Fatty Acyls
    - Subclass Fatty acyl glycosides

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Fatty Acyls
Subclass	Fatty acyl glycosides
Intermediate Tree Nodes	Not available
Direct Parent	Fatty acyl glycosides of mono- and disaccharides
Alternative Parents	Long-chain fatty alcohols Hexoses Alkyl glycosides O-glycosyl compounds Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Fatty acyl glycoside of mono- or disaccharide - Long chain fatty alcohol - Alkyl glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Fatty alcohol - Oxane - Monosaccharide - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
External Descriptors	Not available
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

Names and Identifiers

IUPAC Name	(2R,3R,4S,5S,6R)-2-[(4E,12E)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
INCHI	InChI=1S/C20H28O8/c1-2-3-4-5-7-10-14(23)15(11-8-6-9-12-21)27-20-19(26)18(25)17(24)16(13-22)28-20/h2-3,8,11,14-26H,6,9,12-13H2,1H3/b3-2+,11-8+/t14?,15?,16-,17-,18+,19-,20-/m1/s1
InChIKey	MMMUDYVKKPDZHS-UPPVCQNNSA-N
Smiles	CC=CC#CC#CC(C(C=CCCCO)OC1C(C(C(C(O1)CO)O)O)O)O
Isomeric SMILES	C/C=C/C#CC#CC(C(/C=C/CCCO)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)O
Alternate CAS	129277-38-9
Molecular Weight	396.43
Reaxy-Rn	38014195
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=38014195&ln=

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

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot Number	Certificate Type	Date	Item
L2416561	Certificate of Analysis	Dec 23, 2024	L648060
L2416562	Certificate of Analysis	Dec 23, 2024	L648060
L2416563	Certificate of Analysis	Dec 23, 2024	L648060
L2416564	Certificate of Analysis	Dec 23, 2024	L648060
L2416565	Certificate of Analysis	Dec 23, 2024	L648060
L2416602	Certificate of Analysis	Dec 23, 2024	L648060
L2416603	Certificate of Analysis	Dec 23, 2024	L648060
L2416787	Certificate of Analysis	Dec 23, 2024	L648060
L2416788	Certificate of Analysis	Dec 23, 2024	L648060
L2416793	Certificate of Analysis	Dec 23, 2024	L648060

Chemical and Physical Properties

Solubility	DMSO : 50 mg/mL (126.13 mM; Need ultrasonic) H2O : 50 mg/mL (126.13 mM; Need ultrasonic)
Sensitivity	Light and moisture sensitive
Molecular Weight	396.400 g/mol
XLogP3	-0.600
Hydrogen Bond Donor Count	6
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	9
Exact Mass	396.178 Da
Monoisotopic Mass	396.178 Da
Topological Polar Surface Area	140.000 Å²
Heavy Atom Count	28
Formal Charge	0
Complexity	646.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	2
Defined Bond Stereocenter Count	2
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	2
Covalently-Bonded Unit Count	1

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