Rifamycin S
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Rifamycin S
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CAS No:
13553-79-2
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Formula:
C37H45NO12
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Chemical Name:
Rifamycin S
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Synonyms:
Rifamycin,1,4-dideoxy-1,4-dihydro-1,4-dioxo-;2,7-(Epoxypentadeca[1,11,13]trienimino)naphtho[2,1-b]furan-1,6,9,11(2H)-tetrone,5,17,19,21-tetrahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-,21-acetate;Rifomycin S;2,7-(Epoxypentadeca[1,11,13]trienimino)naphtho[2,1-b]furan,rifamycin deriv.;1,4-Dideoxy-1,4-dihydro-1,4-dioxorifamycin;Rifamycin S;NSC 144130;27184-20-9;959320-39-9;1217878-21-1
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CAS No:
Description
Rifamycin S is a quinone and an antibiotic agnet against Gram-positive bacteria (including MRSA). Rifamycin S is the oxidized forms of a reversible oxidation-reduction system involving two electrons. Rifamycin S generates reactive oxygen species (ROS) and inhibits microsomal lipid peroxidation. Rifamycin S can be used for tuberculosis and leprosy[1][2][3].
Semi-synthetic antibiotic.
Characteristics
194.99000
2.87
Yellow orange crystalline powder
1.3±0.1 g/cm3
180-182 °C
917.4±65.0 °C at 760 mmHg
508.6±34.3 °C
1.605
0mmHg at 25°C
D20 +476° (c = 0.1 in methanol)
Safety Information
KD1925000
|Warning|H302 (25%): Harmful if swallowed [Warning Acute toxicity, oral]|P260, P264, P270, P273, P301+P312, P309+P311, P330, P391, P405, and P501|Aggregated GHS information provided by 4 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Computed Properties
Molecular Weight:695.8
XLogP3:4.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:3
Exact Mass:695.29417587
Monoisotopic Mass:695.29417587
Topological Polar Surface Area:195
Heavy Atom Count:50
Complexity:1480
Defined Atom Stereocenter Count:9
Undefined Bond Stereocenter Count:3
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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