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Surfactin(mixture of isomers) - 95%(mixture of isomers), high purity , CAS No.24730-31-2

COA

Grade & Purity:

Moligand™

≥95%
mixture of isomers

Cas Number: 252023-70-4
Molecular Weight: 1025.04(Average)
EC Number: 607-428-2
PubChem CID: 443592
PubChem SID: 504758805

In stock

Item Number

S329585

Grouped product items
SKU	Size	Availability	Price
S329585-10mg	10mg	3	$38.90
S329585-50mg	50mg	3	$139.90
S329585-250mg	250mg	2	$489.90
S329585-1g	1g	2	$1,489.90

a lipopeptide antibiotic and biosurfactant

View related series

Cytoskeleton (498) Integrin (90) Surfactant (31)

Basic Description

Synonyms	surfactin C \| 3-[(3S,6R,9S,12S,15R,18S,21S,25R)-9-(carboxymethyl)-3,6,15,18-tetrakis(2-methylpropyl)-25-(10-methylundecyl)-2,5,8,11,14,17,20,23-octaoxo-12-propan-2-yl-1-oxa-4,7,10,13,16,19,22-heptazacyclopentacos-21-yl]propanoic acid
Specifications & Purity	Moligand™, ≥95%, mixture of isomers
Biochemical and Physiological Mechanisms	Surfactin is a potent cyclic lipopeptide biosurfactants consists of multiple isomers , which mediates flux of mono-and divalent cations, such as calcium, across lipid bilayer membranes. Surfactin can act as an antimicrobial adjuvant with anti-bacterial, a
Source	Bacillus subtilis
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Grade	Moligand™
Product Description	Surfactin is lipopeptide antibiotic. Powerful biosurfactant resulting in the lysis of erythrocytes and bacteria. Also a clotting inhibitor.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Peptidomimetics
    - Subclass Depsipeptides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Peptidomimetics
Subclass	Depsipeptides
Intermediate Tree Nodes	Not available
Direct Parent	Cyclic depsipeptides
Alternative Parents	Macrolide lactams Alpha amino acid esters Macrolactams Tricarboxylic acids and derivatives Secondary carboxylic acid amides Carboxylic acid esters Lactams Lactones Oxacyclic compounds Azacyclic compounds Carboxylic acids Carbonyl compounds Organopnictogen compounds Hydrocarbon derivatives Organonitrogen compounds Organic oxides
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Cyclic depsipeptide - Macrolide lactam - Alpha-amino acid ester - Macrolactam - Alpha-amino acid or derivatives - Tricarboxylic acid or derivatives - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Secondary carboxylic acid amide - Carboxylic acid - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Azacycle - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Organopnictogen compound - Organic nitrogen compound - Organooxygen compound - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.
External Descriptors	cyclodepsipeptide - lipopeptide antibiotic - macrocyclic lactone
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

Associated Targets(Human)

SIRT1 Tchem NAD-dependent deacetylase sirtuin 1 (3505 Activities)

Discover Target: SIRT1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HST2 NAD-dependent deacetylase HST2 (97 Activities)

Discover Target: HST2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Stachybotrys chartarum (30 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

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

Names and Identifiers

Pubchem Sid	504758805
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504758805
IUPAC Name	3-[(3S,6R,9S,12S,15R,18S,21S,25R)-9-(carboxymethyl)-3,6,15,18-tetrakis(2-methylpropyl)-25-(10-methylundecyl)-2,5,8,11,14,17,20,23-octaoxo-12-propan-2-yl-1-oxa-4,7,10,13,16,19,22-heptazacyclopentacos-21-yl]propanoic acid
INCHI	InChI=1S/C53H93N7O13/c1-30(2)20-18-16-14-13-15-17-19-21-36-28-43(61)54-37(22-23-44(62)63)47(66)55-38(24-31(3)4)48(67)57-40(26-33(7)8)51(70)60-46(35(11)12)52(71)58-41(29-45(64)65)50(69)56-39(25-32(5)6)49(68)59-42(27-34(9)10)53(72)73-36/h30-42,46H,13-29H2,1-12H3,(H,54,61)(H,55,66)(H,56,69)(H,57,67)(H,58,71)(H,59,68)(H,60,70)(H,62,63)(H,64,65)/t36-,37+,38+,39-,40-,41+,42+,46+/m1/s1
InChIKey	NJGWOFRZMQRKHT-WGVNQGGSSA-N
Smiles	CC(C)CCCCCCCCCC1CC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)O1)CC(C)C)CC(C)C)CC(=O)O)C(C)C)CC(C)C)CC(C)C)CCC(=O)O
Isomeric SMILES	CC(C)CCCCCCCCC[C@@H]1CC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)O1)CC(C)C)CC(C)C)CC(=O)O)C(C)C)CC(C)C)CC(C)C)CCC(=O)O
Alternate CAS	24730-31-2
MeSH Entry Terms	surfactin C;surfactin peptide
Molecular Weight	1025.04(Average)

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.

24 results found

Lot Number	Certificate Type	Date	Item
G2504575	Certificate of Analysis	Jun 07, 2025	S329585
G2504576	Certificate of Analysis	Jun 07, 2025	S329585
G2504577	Certificate of Analysis	Jun 07, 2025	S329585
G2504578	Certificate of Analysis	Jun 07, 2025	S329585
B2527542	Certificate of Analysis	Oct 31, 2024	S329585
B2527543	Certificate of Analysis	Oct 31, 2024	S329585
B2527544	Certificate of Analysis	Oct 31, 2024	S329585
I2414316	Certificate of Analysis	Sep 02, 2024	S329585
I2414314	Certificate of Analysis	Sep 02, 2024	S329585
I2414313	Certificate of Analysis	Sep 02, 2024	S329585
I2414315	Certificate of Analysis	Sep 02, 2024	S329585
G2331137	Certificate of Analysis	Jun 29, 2023	S329585
G2331133	Certificate of Analysis	Jun 29, 2023	S329585
G2331127	Certificate of Analysis	Jun 29, 2023	S329585
G2331125	Certificate of Analysis	Jun 29, 2023	S329585
C2401056	Certificate of Analysis	Jun 29, 2023	S329585
G2331121	Certificate of Analysis	Jun 29, 2023	S329585
G2331128	Certificate of Analysis	Jun 29, 2023	S329585
G2331134	Certificate of Analysis	Jun 29, 2023	S329585
F2406042	Certificate of Analysis	Jun 29, 2023	S329585
J2222573	Certificate of Analysis	Jul 11, 2022	S329585
J2222541	Certificate of Analysis	Jul 11, 2022	S329585
J2222542	Certificate of Analysis	Jul 11, 2022	S329585
J2222531	Certificate of Analysis	Jul 11, 2022	S329585

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Chemical and Physical Properties

Solubility	Soluble in ethanol (9.80 - 10.20 mg/ml).
Molecular Weight	1036.300 g/mol
XLogP3	8.800
Hydrogen Bond Donor Count	9
Hydrogen Bond Acceptor Count	13
Rotatable Bond Count	24
Exact Mass	1035.68 Da
Monoisotopic Mass	1035.68 Da
Topological Polar Surface Area	305.000 Å²
Heavy Atom Count	73
Formal Charge	0
Complexity	1800.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	8
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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