R3501

Rifampicin

≥95% (HPLC), powder or crystals

• 동의어(들): 3-(4-Methylpiperazinyliminomethyl)rifamycin SV, Rifampin, Rifamycin AMP
• 실험식(Hill 표기법): C₄₃H₅₈N₄O₁₂
• CAS Number: 13292-46-1
• Molecular Weight: 822.94
• Beilstein: 5723476
• EC Number: 236-312-0
• MDL number: MFCD00151389
• UNSPSC 코드: 51283601
• PubChem Substance ID: 57654590
• NACRES: NA.76

속성

• Quality Level: 200
• 분석: ≥95% (HPLC)
• 양식: powder or crystals
• 색상: Reddish-brown
• pKa: 1.7 (4-hydroxyl group); 7.9 (4-piperazine nitrogen)
• pI: 4.84
• 항생제 활성 스펙트럼: Gram-negative bacteria; Gram-positive bacteria; mycobacteria; viruses
• 동작 모드: protein synthesis | interferes
• 저장 온도: −20°C
• SMILES string: CO[C@H]1\C=C\O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(NC(=O)C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)c(\C=N\N5CCN(C)CC5)c(O)c4c3C2=O

설명

일반 설명

Chemical structure: macrolide

애플리케이션

Rifampicin is used to treat Tuberculosis and Tuberculosis-related mycobacterial infections[1]. It is widely used as an antipruritic agent in the autoimmune cholestatic liver disease, primary biliary cirrhosis (PBC). It has been shown to cause hepatitis[2].

생화학적/생리학적 작용

Inhibits the assembly of DNA and protein into mature virus particles.

Mode of Action: Inhibits initiation of RNA synthesis by binding to β-subunit of RNA polymerase.

Rifampicin inhibits the assembly of DNA and protein into mature virus particles. It inhibits initiation of RNA synthesis by binding to β-subunit of RNA polymerase, which results in cell death[1].

기타 정보

Keep container tightly closed in a dry and well-ventilated place.Product is sensitive to light and moisture.Store under inert gas. Keep in a dry place

안전성 정보

• 픽토그램: GHS07
• 신호어: Warning
• 유해 및 위험 성명서: H302
• 예방조치 성명서: P264 - P270 - P301 + P312 - P501
• Hazard Classifications: Acute Tox. 4 Oral
• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 1
• Flash Point (°F): Not applicable
• Flash Point (°C): Not applicable
• 개인 보호 장비: dust mask type N95 (US), Eyeshields, Gloves