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Lysolipin I - ≥98%, high purity , CAS No.59113-57-4

    Grade & Purity:
  • ≥98%
In stock
Item Number
L274829
Grouped product items
SKU Size
Availability
Price Qty
L274829-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$228.90
L274829-500μg
500μg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$148.90

Broad spectrum antibiotic agent

View related series
Antibiotic (1629) Bacterial (3013)

Basic Description

Synonyms (7R,8R,12S,13R)-22-chloro-3,8,28-trihydroxy-7,12,21-trimethoxy-6-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.02,11.04,9.013,29.018,27.020,25]nonacosa-1(29),2,4(9),10,17,20(25),21,23,27-nonaene-5,26-dione | Lysolipin I | 9H-Xantheno(4',3',2':4,5)(1,3)be
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Broad spectrum antibiotic agent. Shows antibacterial effects against both Gram-negative and Gram-positive bacteria. Induces bacterial cell wall lysis. Interferes with biosynthesis of the bacterial cell wall.
Storage Temp Protected from light,Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Store at -20°C. It is important to note that this product is reported to be light sensitive. Store In the Dark. Store under desiccating conditions.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Benzopyrans
Subclass 1-benzopyrans
Intermediate Tree Nodes Dibenzopyrans - Xanthenes
Direct Parent Xanthones
Alternative Parents Naphthopyranones  Phenanthrenes and derivatives  Chromones  Isoquinolones and derivatives  Naphthols and derivatives  Tetrahydroisoquinolines  Anisoles  1-hydroxy-4-unsubstituted benzenoids  Pyranones and derivatives  Alkyl aryl ethers  Aryl chlorides  Tertiary carboxylic acid amides  Vinylogous acids  Heteroaromatic compounds  Secondary alcohols  Lactams  Polyols  Oxacyclic compounds  Azacyclic compounds  Dialkyl ethers  Acetals  Organopnictogen compounds  Organic oxides  Organonitrogen compounds  Organochlorides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Xanthone - Naphthopyranone - Phenanthrene - Naphthopyran - 1-naphthol - Isoquinolone - Chromone - Naphthalene - Tetrahydroisoquinoline - Anisole - 1-hydroxy-4-unsubstituted benzenoid - Pyranone - Alkyl aryl ether - Benzenoid - Pyran - Aryl chloride - Aryl halide - Heteroaromatic compound - Vinylogous acid - Tertiary carboxylic acid amide - Carboxamide group - Secondary alcohol - Lactam - Acetal - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Ether - Azacycle - Polyol - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.
External Descriptors Not available

Names and Identifiers

IUPAC Name (7R,8R,12S,13R)-22-chloro-3,8,28-trihydroxy-7,12,21-trimethoxy-6-methyl-14,16,19-trioxa-6-azaheptacyclo[15.11.1.02,11.04,9.013,29.018,27.020,25]nonacosa-1(29),2,4(9),10,17,20(25),21,23,27-nonaene-5,26-dione
INCHI InChI=1S/C29H24ClNO11/c1-31-28(36)14-10(19(33)29(31)39-4)7-11-13(20(14)34)15-16-25(22(11)37-2)40-8-41-26(16)27-17(21(15)35)18(32)9-5-6-12(30)24(38-3)23(9)42-27/h5-7,19,22,25,29,33-35H,8H2,1-4H3/t19-,22+,25-,29-/m1/s1
InChIKey NEOMIZJYHXSRLV-MVHMQXOSSA-N
Smiles CN1C(C(C2=C(C1=O)C(=C3C(=C2)C(C4C5=C3C(=C6C(=C5OCO4)OC7=C(C6=O)C=CC(=C7OC)Cl)O)OC)O)O)OC
Isomeric SMILES CN1[C@@H]([C@@H](C2=C(C1=O)C(=C3C(=C2)[C@@H]([C@H]4C5=C3C(=C6C(=C5OCO4)OC7=C(C6=O)C=CC(=C7OC)Cl)O)OC)O)O)OC
Molecular Weight 597.95
Reaxy-Rn 53183142
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=53183142&ln=

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

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

Chemical and Physical Properties

Solubility Soluble in DMSO
Sensitivity light sensitive
Molecular Weight 598.000 g/mol
XLogP3 3.000
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 11
Rotatable Bond Count 3
Exact Mass 597.104 Da
Monoisotopic Mass 597.104 Da
Topological Polar Surface Area 153.000 Ų
Heavy Atom Count 42
Formal Charge 0
Complexity 1080.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 4
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

Solution Calculators

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