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Lactonamycin

CAT: 0013-GTR19254537-02Size: 50 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19254537-02Size:50 mg
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Description
Lactonamycin exhibits significant activity against Gram-positive bacteria, including Staphylococcus, Streptococcus, Enterococcus, MRSA (MIC of 0.39-0.78 μg/mL), and VRE (MIC of 0.39-0.78 μg/mL) . It also demonstrates inhibitory effects on various tumor cell lines such as L-1210, P388, S180, FS-3, Ehrlich, and B16-BL5 (IC50 of 0.06-3.3 μg/mL) .
CAS Number
182234-02-2
Field of Research
Infectious Disease & Virology
Smiles
O ([C@]12[C@]3 ([C@@] (OC) (OC1) CC (=O) O3) C (=O) C=4C (C2=O) =CC=5C (C4O) =C6C (=C (O) C5) C (=O) N (C) C6) [C@@H]7O[C@@H] (C) [C@@H] (O) CC7
Molecular Formula
C28H27NO12
Molecular Weight
569.513
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

(3aS,5aS,14aR)-3,3a,11,12-Tetrahydro-9,13-dihydroxy-3a-methoxy-11-methyl-5a-(((2S,5S,6S)-tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)oxy)-2H,5H-furo(2'',3'':4',5')furo(3',4':6,7)naphth(2,3-e)isoindole-2,6,10,14(5aH)-tetrone

Lactonamycin is an organic heterohexacyclic compound isolated from the culture broth of Streptomyces rishiriensis. It is an antibiotic with antibacterial activity. It has a role as a metabolite, an antimicrobial agent and an antibacterial agent. It is a member of phenols, a gamma-lactone, an organic heterohexacyclic compound and a trideoxyhexose derivative. It is functionally related to a L-rhodinose.

CAS Number182234-02-2
PubChem CID10370774
IUPAC Name(15S,18S,22R)-2,9-dihydroxy-15-[(2S,5S,6S)-5-hydroxy-6-methyloxan-2-yl]oxy-18-methoxy-6-methyl-17,21-dioxa-6-azahexacyclo[11.10.0.03,11.04,8.015,22.018,22]tricosa-1(13),2,4(8),9,11-pentaene-7,14,20,23-tetrone
Molecular FormulaC28H27NO12
Molecular Weight569.5
XLogP0.9
Topological Polar Surface Area178
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count12
Rotatable Bond Count3
Heavy Atom Count41
Formal Charge0
Complexity1190
SMILES
C[C@H]1[C@H](CC[C@@H](O1)O[C@@]23CO[C@@]4([C@@]2(C(=O)C5=C(C3=O)C=C6C=C(C7=C(C6=C5O)CN(C7=O)C)O)OC(=O)C4)OC)O
InChI
InChI=1S/C28H27NO12/c1-11-15(30)4-5-18(39-11)41-26-10-38-27(37-3)8-17(32)40-28(26,27)24(35)21-13(23(26)34)6-12-7-16(31)20-14(19(12)22(21)33)9-29(2)25(20)36/h6-7,11,15,18,30-31,33H,4-5,8-10H2,1-3H3/t11-,15-,18-,26+,27-,28-/m0/s1
InChIKey
XFQJOLWXLJXJSV-VUAGTGNDSA-N
Chemical Structure
2D Structure
2D structure of (3aS,5aS,14aR)-3,3a,11,12-Tetrahydro-9,13-dihydroxy-3a-methoxy-11-methyl-5a-(((2S,5S,6S)-tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)oxy)-2H,5H-furo(2'',3'':4',5')furo(3',4':6,7)naphth(2,3-e)isoindole-2,6,10,14(5aH)-tetrone
CAS: 182234-02-2
CID: 10370774
Formula: C28H27NO12
MW: 569.5
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight569.5
XLogP30.9
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count12
Rotatable Bond Count3
Exact Mass569.15332530
Monoisotopic Mass569.15332530
Topological Polar Surface Area178 Ų
Heavy Atom Count41
Formal Charge0
Complexity1190
Isotope Atom Count0
Defined Atom Stereocenter Count6
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

Alternative Products

CatalogName
HY-N14722Lactonamycin
TN10215-01Lactonamycin Z

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