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Ramoplanin

CAS No.
76168-82-6
Chemical Name:
Ramoplanin
Synonyms
A 16686;A 16686A;Ramoplanin;Ramoplaninr;Ray mora ning;Antibiotic A 16686;RaMoplanin coMplex;RaMoplanin(A 16686,A 16686A)
CBNumber:
CB61074884
Molecular Formula:
C106H170ClN21O30
Molecular Weight:
2254.0597
MDL Number:
MFCD01775776
MOL File:
76168-82-6.mol
Last updated:2024-10-23 13:36:13

Ramoplanin Properties

Melting point 210-230°
alpha D20 +78.3° (c = 1.04 in H2O)
storage temp. -20°C
solubility H2O: soluble10mg/mL
form powder
color White to Off-White
InChIKey FSBZBQUUCNYWOK-KFTDLNJOSA-N
EWG's Food Scores 1
FDA UNII 0WX9996O2G

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H318
Precautionary statements  P280-P305+P351+P338
Hazard Codes  Xi
Risk Statements  41
Safety Statements  26-39
WGK Germany  nwg
RTECS  VE5050000
Toxicity LD50 in mice (mg/kg): 328 i.p., 122 i.v.; orally in rats: 2000 mg/kg (Pallanza)
NFPA 704
0
3 0

Ramoplanin price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich R1781 Ramoplanin ≥75% (as ramoplanin A2) 76168-82-6 250mg $385 2024-03-01 Buy
Cayman Chemical 28189 Ramoplanin Complex 76168-82-6 10mg $44 2024-03-01 Buy
Cayman Chemical 28189 Ramoplanin Complex 76168-82-6 250mg $321 2024-03-01 Buy
Cayman Chemical 28189 Ramoplanin Complex 76168-82-6 50mg $130 2024-03-01 Buy
Cayman Chemical 28189 Ramoplanin Complex 76168-82-6 100mg $172 2024-03-01 Buy
Product number Packaging Price Buy
R1781 250mg $385 Buy
28189 10mg $44 Buy
28189 250mg $321 Buy
28189 50mg $130 Buy
28189 100mg $172 Buy

Ramoplanin Chemical Properties,Uses,Production

Mode of action

The lipid carrier involved in transporting the cell wall building block across the membrane is a C55 isoprenyl phosphate. The lipid acquires an additional phosphate group in the transport process and must be dephosphorylated in order to regenerate the native compound for another round of transfer. Ramoplanin as cyclic peptide antibiotics binds to the C55 lipid carrier. Ramoplanin prevents it from participating in transglycosylation thus disrupting the lipid carrier cycle.

Description

Ramoplanin (A 16686, A16686A, MDL 62198) is a novel oral nonabsorbable 17-amino-acid cyclic lipoglycodepsipeptide antibiotic from Biosearch Italy. Ramoplanin is an antibiotic complex, first identified in 1984, that was isolated from the fermentation broth of Actinoplanes sp. ATCC 33076. It is a mixture of three closely related compounds, ramoplanin A1–A3, which differ only in the acyl group attached to the Asn-1 N-terminus; ramoplanin A2 is the most abundant.

Uses

Ramoplanin is a potent cyclic lipoglycodepsipeptide antibiotic that exhibits wide spectrum of antibiotic properties against gram-positive and gram-negative bacteria.

Uses

Ramoplanin is a complex of three high molecular weight glycolipodepsipeptides, varying in the chain length and shape of the dieneone lipid side-chain. Ramoplanin was isolated in the early 1980s as the major metabolite of a strain of Actinoplanes with antiviral and antibiotic activity against drug resistant Gram positive isolates. Ramoplanin acts by inhibiting cell wall biosynthesis via a different mechanism from the vancomycin-related glycopeptides.

Antimicrobial activity

Ramoplanin displays activity against aerobic and anaerobic Grampositive bacteria by preventing cell wall peptidoglycan formation through binding to a key intermediate moiety, lipid II, and thereby disrupting bacterial cell wall synthesis. The primary use of ramoplanin is in the treatment of Clostridium difficile infections.

Mechanism of action

The mechanism of action of ramoplanin involves sequestration of peptidoglycan biosynthesis lipid intermediates, thus physically occluding these substrates from proper utilization by the latestage peptidoglycan biosynthesis enzymes MurG and the transglycosylases (TGases). Ramoplanin is structurally related to two cell wall-active lipodepsipeptide antibiotics, janiemycin and enduracidin, and is functionally related to members of the lantibiotic class of antimicrobial peptides (mersacidin, actagardine, nisin, and epidermin) and glycopeptide antibiotics. As a consequence of its unique mechanism of action, cross-resistance with existing glycopeptides and beta-lactam antibiotics has not been observed.

Pharmacokinetics

Ramoplanin is not absorbed from the intestinal tract. When ramoplanin (200 and 400 mg) was administered orally to two groups of healthy volunteers over a period of 10 days, no ramoplanin could be detected in plasma and urine. With the 200-mg dose, concentrations in stools varied between 467 and 1043 mg/g, and with the 400-mg dose, concentrations were between 765 and 2032 mg/g. Results from an in vitro gut model and hamster model revealed that ramoplanin may be more effective than vancomycin at killing spores and preventing spore recrudescence.

Toxicology

When administered orally in a double-blind randomized placebocontrolled study, no adverse reactions were observed in patients receiving two daily doses of ramoplanin (100 or 400 mg) in comparison with the placebo. Single and repeated topical application in ten healthy human volunteers revealed very low irritation rates and no sensitization after 21 days.

Ramoplanin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 92)Suppliers
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AFINE CHEMICALS LIMITED
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Hebei Miaoyin Technology Co.,Ltd
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Aladdin Scientific
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Hangzhou J&H Chemical Co., Ltd. 0571-+86-571-87396432 sales@jhechem.com China 11578 59

View Lastest Price from Ramoplanin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ramoplanin pictures 2024-10-24 Ramoplanin
76168-82-6
US $45.00 / mg 10g TargetMol Chemicals Inc.
  • Ramoplanin pictures
  • Ramoplanin
    76168-82-6
  • US $45.00 / mg
  • TargetMol Chemicals Inc.
A 16686 A 16686A Antibiotic A 16686 RaMoplanin(A 16686,A 16686A) RaMoplanin coMplex Ramoplanin Ramoplaninr Ray mora ning 76168-82-6 6168-82-6 C106H170ClN21O30