Mode of action
ChemicalBook > CAS DataBase List > Fusidine

Fusidine

Mode of action
Product Name
Fusidine
CAS No.
6990-06-3
Chemical Name
Fusidine
Synonyms
FUSIDIC ACID;Fusidinic acid;(Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethyldodecahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)-ylidene)-6-methylhept-5-enoic acid;Fusidic acid CRS;29-NordaMMara-17(20),24-dien-21-oicacid, 16-(acetyloxy)-3,11-dihydroxy-, (3a,4a,8a,9b,11a,13a,14b,16b,17Z)-;(3ALPHA,4ALPHA,8ALPHA,9BETA,11ALPHA,13ALPHA,14BETA,16BETA,17Z)-16-(ACETYLOXY)-3,11-DIHYDROXY-29-NORDAMMARA-17(20),24-DIEN-21-OIC ACID;sq16603;ramycin;Fuzidin;Flucidin
CBNumber
CB8431174
Molecular Formula
C31H48O6
Formula Weight
516.72
MOL File
6990-06-3.mol
More
Less

Fusidine Property

Melting point:
190-192°C
Boiling point:
521.49°C (rough estimate)
alpha 
D20 -9° (chloroform)
Density 
1.0389 (rough estimate)
vapor pressure 
0-0Pa at 25℃
refractive index 
1.4890 (estimate)
storage temp. 
Sealed in dry,2-8°C
solubility 
Practically insoluble in water, freely soluble in ethanol (96 per cent)
pka
pK: 5.35 in water
form 
Solid
color 
White to Off-White
optical activity
-920 (c 1, CHCl3)
Water Solubility 
2.376-525000μg/L at 25℃
λmax
204nm(H2O)(lit.)
Merck 
14,4317
Stability:
Hygroscopic
LogP
2.68-6.75 at 20℃
CAS DataBase Reference
6990-06-3(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36
WGK Germany 
3
RTECS 
RC1350000
HS Code 
29419000
Toxicity
LD50 in mice (g/kg): 1.2 s.c.; 1.5 orally (Godtfredsen)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
Y0001411
Product name
Fusidic acid
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
y0001411
Price
$220
Updated
2024/03/01
Sigma-Aldrich
Product number
Y0001394
Product name
Fusidic acid for peak identification
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
y0001394
Price
$153
Updated
2024/03/01
Sigma-Aldrich
Product number
PHR2810
Product name
Fusidic acid
Purity
certified reference material, pharmaceutical secondary standard
Packaging
50MG
Price
$344
Updated
2024/03/01
TCI Chemical
Product number
F1007
Product name
Fusidic Acid
Purity
>97.0%(HPLC)(T)
Packaging
1g
Price
$230
Updated
2024/03/01
TCI Chemical
Product number
F1007
Product name
Fusidic Acid
Purity
>97.0%(HPLC)(T)
Packaging
5g
Price
$809
Updated
2024/03/01
More
Less

Fusidine Chemical Properties,Usage,Production

Mode of action

Fusidic acid forms a stable complex with an elongation factor (EF-G) involved in translocation and with guanosine triphosphate (GTP), which provides energy for the translocation process. One round of translocation occurs, with hydrolysis of GTP, but the fusidic acid–EF-G–GDP complex cannot dissociate from the ribosome, thereby blocking further chain elongation and leaving peptidyl-tRNA in the P site.
Although protein synthesis in Gram-negative bacilli–and, indeed, mammalian cells–is susceptible to fusidic acid, the antibiotic penetrates poorly into these cells and the spectrum of action is virtually restricted to Gram-positive bacteria, notably staphylococci.

Description

Fusidic acid was found in the culture broth of a fungus imperfectus, Fusidium coccineum, by Leo in 1962. It has a steroid struc ture but shows no hormonal activity.

Chemical Properties

White Solid

Uses

antibacterial

Uses

Fusidic acid is a bacteriostatic antibiotic. Fusidic Acid suppresses nitric oxide lysis of pancreatic islet cells. Inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA. Dyes and metabolites.

Definition

ChEBI: A steroid antibiotic that is isolated from the fermentation broth of Fusidium coccineum.

brand name

Fucidine (Bristol-Myers Squibb).

Hazard

Moderately toxic inhibitor of translocation during protein synthesis.

Biological Activity

Fusidic acid shows very strong activity against Staphy lococcus aureus and weak activity against other gram-positive bacteria and gram-negative cocci and Mycobacterium.

Biochem/physiol Actions

Fusidic acid is a tetracyclic triterpenoid with antibiotic activity against Gram-positive bacteria. It is derived from Fusidium coccineum. It shows its activity against anaerobes, corynebacterial, Nocardia, and Neisseria species. Fusidic acid exhibits therapeutic effects against Staphylococcal infections, skin infections.

Fusidine Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Fusidine Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Target molecule Corp.
Tel
857-239-0968
Fax
857-239-8801
Email
service1@targetmol.com
Country
United States
ProdList
2559
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
BOC Sciences
Tel
16314854226; +16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19741
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
Cato Research Chemicals Inc.
Tel
020-81215950 4000-868-328
Email
customer@uwalab.com
Country
United States
ProdList
10404
Advantage
58
TargetMol Chemicals Inc.
Tel
Email
support@targetmol.com
Country
United States
ProdList
38632
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Wonda Science
Tel
--
Fax
--
Email
wonda@wondascience.com
Country
United States
ProdList
2192
Advantage
50
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
More
Less

View Lastest Price from Fusidine manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Fusidine 6990-06-3
Price
US $0.00/KG
Min. Order
1KG
Purity
97.5%-101%; EP
Supply Ability
100KGS
Release date
2021-06-17
Sinoway Industrial co., ltd.
Product
Fusidic Acid 6990-06-3
Price
US $0.00/Kg/Bag
Min. Order
2Kg/Bag
Purity
97.5% up / EP
Supply Ability
20 tons
Release date
2021-07-23
HangZhou RunYan Pharma Technology Co.,LTD.
Product
Fusidine,Fusidic acid 6990-06-3
Price
US $0.00-0.00/g
Min. Order
10000g
Purity
99.0%min. HPLC
Supply Ability
1000kg
Release date
2024-09-12

6990-06-3, FusidineRelated Search:


  • 4-alpha,8-alpha,9-beta,11-alpha,13-alpha,14-beta,16-beta,17z)-ph
  • ramycin
  • sq16603
  • (3ALPHA,4ALPHA,8ALPHA,9BETA,11ALPHA,13ALPHA,14BETA,16BETA,17Z)-16-(ACETYLOXY)-3,11-DIHYDROXY-29-NORDAMMARA-17(20),24-DIEN-21-OIC ACID
  • FUSIDIC ACID
  • 29-NordaMMara-17(20),24-dien-21-oicacid, 16-(acetyloxy)-3,11-dihydroxy-, (3a,4a,8a,9b,11a,13a,14b,16b,17Z)-
  • Fusidic acid for peak identification
  • Fusidic acid, 98.5%
  • (Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethyldodecahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)-ylidene)-6-methylhept-5-enoic acid
  • -16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethyldodecahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)
  • -2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)
  • -6-methylhept-5-enoic acid
  • 29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-
  • (3a,4a,8a,9b,11a,13a,14b,16b,17Z)-16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic Acid
  • Flucidin
  • Fucithalmic
  • Fusidinic acid
  • NSC 56192
  • 29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, (3.alpha.,4.alpha.,8.alpha.,9.beta.,11.alpha.,13.alpha.,14.beta.,16.beta.,17Z)-
  • 16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic acid
  • Fusidine
  • 24-dien-21-oicacid,16-(acetyloxy)-3,11-dihydroxy-29-nordammara-17(20(3-al
  • FUSIDIC ACID IP
  • (4S,8α,9β,13α,14β,17Z)-16β-Acetoxy-3α,11α-dihydroxy-29-nor-5α-dammara-17(20),24-dien-21-oic acid
  • (8α,9β,13α,14β,Z)-16β-Acetyloxy-3α,11α-dihydroxy-29-nordammara-17(20),24-dien-21-oic acid
  • Fuzidin
  • Fusidate Acid
  • Pyzidieb acid
  • (3a,4a,8a,9,11a,13a,147,167,17Z)-16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic Acid
  • (3α,4α,8α,9β,11α,13α,147β,167β,17Z)-16-(Acetyloxy)-3,11-dihydroxy-29-nordaMMara-17(20),24-dien-21-oic Acid
  • Fusidic acid for peak identification CRS
  • FusidicAcid&gt
  • Fusidic acid CRS
  • Fusidine USP/EP/BP
  • Fusidine,Fusidic acid
  • Fusidic acid-D6Q: What is Fusidic acid-D6 Q: What is the CAS Number of Fusidic acid-D6 Q: What is the storage condition of Fusidic acid-D6
  • Fusidic AcidQ: What is Fusidic Acid Q: What is the CAS Number of Fusidic Acid Q: What is the storage condition of Fusidic Acid Q: What are the applications of Fusidic Acid
  • fusidicaci
  • Fusidie acid
  • Amlexanox Impurity 7
  • 6990-06-3
  • 3990-06-3
  • 6990-6-3
  • C31H48O6
  • Antibiotics A to Z
  • Antibiotics A-F
  • Antibiotics
  • BioChemical
  • Inhibitors
  • Intermediates & Fine Chemicals
  • API
  • FUCIDINE
  • antibiotic
  • Pharmaceuticals
  • Steroids
  • E-FCell Signaling and Neuroscience
  • Gene Regulation and Expression
  • RNA-Protein Translation Inhibitors