GLPBio

Lagosin

Catalog No.: GC11791Purity:>96.00%Synonyms: Antibiotic A 246,14-hydroxy Filipin,NSC 105388,NSC 276732
Lagosin is a polyene macrolide antibiotic.

Products are for research use only. Not for human use. We do not sell to patients.


Lagosin
Cas No.: 6834-98-6
10mM (in 1mL DMSO)In Stock
$517.00
1
1mgIn Stock
$140.00
1
5mgIn Stock
$350.00
1
10mgIn Stock
$560.00
1
25mgIn Stock
$1,008.00
1
50mgIn Stock
$1,512.00
1
100mgIn Stock
$2,170.00
1

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Description

Lagosin is a polyene macrolide antibiotic. Lagosin exerts its antifungal effects by interacting with membrane sterols and possesses broad-spectrum antifungal and antitumor activities. Lagosin can be used in research related to antifungal infections and antitumor studies[1-4].

In vitro, Lagosin (1-2μg/ml) was used to treat Chinese hamster V79 cells for 2 hours, followed by stimulation with [14C]bleomycin A2. Lagosin significantly enhanced the cellular uptake of [14C]bleomycin A2[5]. Lagosin (50μg/ml) was used to treat L-form cells of Escherichia coli W1655F+ for 6 hours. Lagosin inhibited the growth of the L-form cells[6].

In vivo, Lagosin (20mg/kg; single injection) was administered via intraperitoneal injection to Balb/C mice bearing EMT6 solid tumors. Lagosin alone did not exhibit significant cytotoxicity against the tumor cells[6].

References:
[1] Dembitsky VM, Terent'ev AO, Baranin SV, et al. Boron's Double Edge-Antibiotics, Toxins, and the Fine Line Between Them. Molecules. 2026 Mar 18;31(6):1021.
[2] Peng C, An D, Ding WX, et al. Fungichromin production by Streptomyces sp. WP-1, an endophyte from Pinus dabeshanensis, and its antifungal activity against Fusarium oxysporum. Appl Microbiol Biotechnol. 2020 Dec;104(24):10437-10449.
[3] Pandey RC, Guenther EC, Aszalos AA, et al. Physicochemical and biological comparison of polyene macrolide antibiotics fungichromin, lagosin and cogomycin. J Antibiot (Tokyo). 1982 Aug;35(8):988-96.
[4] Arora HR. Effects of polyene antibiotics on the heart. A study with nystatin and lagosin. Med Pharmacol Exp Int J Exp Med. 1965;13(3):155-60.
[5] Akiyama SI, Hidaka K, Komiyama S, et al. Control of permeation of bleomycin A2 by polyene antibiotics in cultured Chinese hamster cells. Cancer Res. 1979 Dec;39(12):5150-4.
[6] Twentyman PR. The effect of bleomycin and pentamycin in combination on the survival of EMT6 mouse tumour cells in vitro and in vivo. Br J Cancer. 1976 Apr;33(4):459-64.

Protocol

Cell experiment [1]:

Cell lines

Chinese hamster V79 cells

Preparation Method

Chinese hamster V79 cells were maintained in minimal essential medium supplemented with 10% fetal bovine serum. Cells were treated with Lagosin and bleomycin A2 for specified durations.

Reaction Conditions

4-12μg/ml; 2h pretreatment

Applications

Lagosin significantly enhanced the cellular uptake of [14C]bleomycin A2 by 2- to 4-fold. Lagosin synergistically inhibited DNA synthesis and colony-forming activity when combined with bleomycin A2.

Animal experiment [2]:

Animal models

Balb/C mice bearing EMT6 solid tumours

Preparation Method

Lagosin was suspended in 0.5% carboxymethyl cellulose in Hanks' solution and injected intraperitoneally (i.p.). Tumours were treated when they reached a size of around 150mm³ (Day 9-10 post-inoculation).

Dosage form

20mg/kg; i.p.; single injection

Applications

Lagosin alone was not very cytotoxic to the tumour cells in vivo.

References:
[1] Akiyama SI, Hidaka K, Komiyama S, et al. Control of permeation of bleomycin A2 by polyene antibiotics in cultured Chinese hamster cells. Cancer Res. 1979 Dec;39(12):5150-4.
[2] Twentyman PR. The effect of bleomycin and pentamycin in combination on the survival of EMT6 mouse tumour cells in vitro and in vivo. Br J Cancer. 1976 Apr;33(4):459-64.

Product Documents

Purity:>96.00%Appearance:A solid

Chemical Properties

CAS No.
6834-98-6
Synonyms
Antibiotic A 246,14-hydroxy Filipin,NSC 105388,NSC 276732
Chemical Name
(3R,4S,6S,8S,10R,12R,14R,15R,16R,17E,19E,21E,23E,25E,27S,28R)-4,6,8,10,12,14,15,16,27-nonahydroxy-3-[(1R)-1-hydroxyhexyl]-17,28-dimethyl-oxacyclooctacosa-17,19,21,23,25-pentaen-2-one
SMILES
C/C1=C\C=C\C=C\C=C\C=C\[C@H](O)[C@@H](C)OC([C@@]([C@H](O)CCCCC)([H])[C@@H](O)C[C@@H](O)C[C@@H](O)C[C@@H](O)C[C@@H](O)C[C@@H](O)[C@@H](O)[C@@H]1O)=O
Molecular Formula
C35H58O12
Molecular Weight
670.8
Solubility
DMF: Soluble,DMSO: Soluble,Ethanol: Soluble,Methanol: Soluble
Storage
4°C, protect from light
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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