N1271

Narasin from Streptomyces auriofaciens

≥98% (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 55134-13-9

Synonym(S): 4-methylsalinomycin, Monteban, narasin A

Select a Size

Pack Size SKU Availability Price
5 MG N1271-5-MG In Stock ₹ 14,289.00
25 MG N1271-25-MG In Stock ₹ 66,855.20
50 MG N1271-50-MG In Stock ₹ 1,25,851.45

N1271 - 5 MG

₹ 14,289.00

In Stock

Quantity

1

Base Price: ₹ 14,289.00

GST (18%): ₹ 2,572.02

Total Price: ₹ 16,861.02

Quality Level

200

Assay

≥98% (HPLC)

form

powder

solubility

methanol: soluble 20 mg/mL

antibiotic activity spectrum

Gram-positive bacteriafungiviruses

Mode of action

cell membrane | interferes

storage temp.

−20°C

SMILES string

CCC(C1OC(C(C)CC1C)C(C)C(O)C(C)C(=O)C(CC)C2OC3(OC4(CCC(C)(O4)C5CCC(O)(CC)C(C)O5)C(O)C=C3)C(C)CC2C)C(O)=O

InChI

1S/C43H72O11/c1-12-30(35(46)27(8)34(45)28(9)36-23(4)21-24(5)37(51-36)31(13-2)39(47)48)38-25(6)22-26(7)42(52-38)18-15-32(44)43(54-42)20-19-40(11,53-43)33-16-17-41(49,14-3)29(10)50-33/h15,18,23-34,36-38,44-45,49H,12-14,16-17,19-22H2,1-11H3,(H,47,48)

InChI key

VHKXXVVRRDYCIK-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
1457458
Narasin
Sigma Aldrich ₹ 54,211.60

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Description

  • Application: Narasin is a growth-promoting ionophoric antibacterial agent for Enterococci, specifically Enterococcus faecium and Enterococcus faecalis[1][2]. It inhibits coccidial infection in poultry and mammals and is used in studies involving sodium calcium ion exchange.
  • Biochem/physiol Actions: Narasin administration in swine results in improved nitrogen digestibility, which decreases fecal nitrogen and increases the relative concentrations of propionic acid in the large intestine. Polyether ionophores, such as Narasin, have a hydrophilic interior and a hydrophobic exterior. The lipophilic ionophore attaches to the lipid rich cell membranes of Gram-positive bacteria. Ionophores bind Na+, K+, and H+ and facilitate their transfer across the bacterial cell membrane, resulting in an increase in H+ concentration on the inside of the Gram-positive cell. Therefore, the H+ ATPase pump is activated to transport out excess H+. The cell is depleted of its energy resources and reduces fermentative functions and cell division [3].

SAFETY INFORMATION

Pictograms

GHS06

Signal Word

Danger

Hazard Statements

H300

Precautionary Statements

P264 - P270 - P301 + P310 - P405 - P501

Hazard Classifications

Acute Tox. 2 Oral

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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N1271

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Quality Level:
200

Assay:
≥98% (HPLC)

form:
powder

solubility:
methanol: soluble 20 mg/mL

antibiotic activity spectrum:
Gram-positive bacteriafungiviruses

Mode of action:
cell membrane | interferes

storage temp.:
−20°C

SMILES string:
CCC(C1OC(C(C)CC1C)C(C)C(O)C(C)C(=O)C(CC)C2OC3(OC4(CCC(C)(O4)C5CCC(O)(CC)C(C)O5)C(O)C=C3)C(C)CC2C)C(O)=O

InChI:
1S/C43H72O11/c1-12-30(35(46)27(8)34(45)28(9)36-23(4)21-24(5)37(51-36)31(13-2)39(47)48)38-25(6)22-26(7)42(52-38)18-15-32(44)43(54-42)20-19-40(11,53-43)33-16-17-41(49,14-3)29(10)50-33/h15,18,23-34,36-38,44-45,49H,12-14,16-17,19-22H2,1-11H3,(H,47,48)

InChI key:
VHKXXVVRRDYCIK-UHFFFAOYSA-N

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SMILES string:
OCc1ccccc1[N+]([O-])=O

InChI:
1S/C7H7NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,9H,5H2

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BWRBVBFLFQKBPT-UHFFFAOYSA-N

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OCc1ccc(cc1)[N+]([O-])=O

InChI:
1S/C7H7NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,9H,5H2

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JKTYGPATCNUWKN-UHFFFAOYSA-N

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SMILES string:
COc1ccc2C(OC(=O)c2c1OC)C3N(C)CCc4cc5OCOc5c(OC)c34

InChI:
1S/C22H23NO7/c1-23-8-7-11-9-14-20(29-10-28-14)21(27-4)15(11)17(23)18-12-5-6-13(25-2)19(26-3)16(12)22(24)30-18/h5-6,9,17-18H,7-8,10H2,1-4H3/t17-,18+/m1/s1

InChI key:
AKNNEGZIBPJZJG-MSOLQXFVSA-N