利福霉素
- 中文名称:
- 利福霉素
- 中文别名:
- 利福霉素;
Phenylseleninic acid;
Benzeneseleninic acid;
3-Amino-4-pyrazolecarboxylic acid ethyl ester;
Konjac Glucomannan Powder;
3-Amino-4-carbethoxypyrazole;
4-(2,5-dichlorophenyl)azo-3-hydroxy-N-(2-oxo-1,3-dihydrobenzimidazol-5-yl)naphthalene-2-carboxamide;
Pigment Brown 25;
4-[(2,5-dichlorophenyl)azo]-N-(2,3-dihydro-2-oxo-1H-benzimidazol-5-yl)-3-hydroxynaphthalene-2-carboxamide;
Ormetoprimum;
Ormetoprimum [INN-Latin];
Ormetorprim;
Ro 5-9754;
UNII-M3EFS94984
- 英文名称:
- Rifamycin (9CI)
- 英文别名:
- rifamycin SV;
RIFAMYCIN SV;
Acetic acid,((1,2-dihydro-5,6,17,19,21-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-2,7-(epoxypentadeca(1,11,13)trienimino)naphtho(2,1-b)furan-9-yl)oxy)-,21-acetate,1,2,2-tripropylhydrazide;
rifamycin-S;
(12S,3E,5S,13E,15Z)-7t-acetoxy-15,6,9,9c,11t-pentahydroxy-5r-methoxy-12,4,6t,8c,10c,12t,16-heptamethyl-2-oxa-18-aza-1(2,7)-naphtho[2,1-b]furana-cyclooctadecaphane-3,13,15-triene-11,17-dione;
O4-(tripropylhydrazinocarbonyl-methyl)-rifamycin;
Rifamycin,4-O-(2-oxo-2-(tripropylhydrazino)ethyl);
rifamycin-B tripropylhydrazide;
Rifamycin-B-tripropyl-hydrazid
- CAS No.:
- 6998-60-3
- 分 子 式:
-
C37H47NO12
- 分 子 量:
- 697.76900
- 精确分子量:
- 697.31000
- PSA:
- 201.31000
- EINECS:
- 230-273-3
- InChI:
- InChI=1/C37H47NO12/c1-16-11-10-12-17(2)36(46)38-23-15-24(40)26-27(32(23)44)31(43)21(6)34-28(26)35(45)37(8,50-34)48-14-13-25(47-9)18(3)33(49-22(7)39)20(5)30(42)19(4)29(16)41/h10-16,18-20,25,29-30,33,40-44H,1-9H3,(H,38,46)/b11-10+,14-13+,17-12-/t16-,18+,19+3
- 分子结构式:
-
- SDS:
- 查看
利福霉素 毒理性
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- KD1922000
- CHEMICAL NAME :
- 2,7-(Epoxypentadeca(1,11,13)trienimino)naphtho(2,1-b)
furan-1,11(2H)-dione,
5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,18,20
,22-heptamethyl-, 21-acetate
- CAS REGISTRY NUMBER :
- 6998-60-3
- LAST UPDATED :
- 199509
- DATA ITEMS CITED :
- 11
- MOLECULAR FORMULA :
- C37-H47-N-O12
- MOLECULAR WEIGHT :
- 697.85
- WISWESSER LINE NOTATION :
- T C6 B65-24- A D E 2BC G& AV LO NO F&VM OU B&U D&U
MH&&&TJ DQ GQ IQ J1 M1 QO1 R1 SOV1 T1 UQ V
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 2120 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 625 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 450 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intracerebral
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 5800 ug/kg
- TOXIC EFFECTS :
- Behavioral - convulsions or effect on seizure threshold
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- DOSE :
- 700 mg/kg
- SEX/DURATION :
- female 7-13 day(s) after conception
- TOXIC EFFECTS :
- Reproductive - Specific Developmental Abnormalities - musculoskeletal system
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- DOSE :
- 500 mg/kg
- SEX/DURATION :
- female 2 day(s) after conception
- TOXIC EFFECTS :
- Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death,
e.g., stunted fetus)
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- DOSE :
- 900 mg/kg
- SEX/DURATION :
- female 8-16 day(s) after conception
- TOXIC EFFECTS :
- Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death,
e.g., stunted fetus)
Reproductive - Specific Developmental Abnormalities - musculoskeletal system
Reproductive - Effects on Newborn - growth statistics (e.g.%, reduced weight
gain)
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- DOSE :
- 1800 mg/kg
- SEX/DURATION :
- female 8-16 day(s) after conception
- TOXIC EFFECTS :
- Reproductive - Fertility - post-implantation mortality (e.g. dead and/or
resorbed implants per total number of implants)
MUTATION DATA
- TYPE OF TEST :
- Cytogenetic analysis
- TEST SYSTEM :
- Rodent - mouse Mammary gland
- DOSE/DURATION :
- 6300 nmol/L/24H (Continuous)
- REFERENCE :
- JTSCDR Journal of Toxicological Sciences. (Japanese Soc. of Toxicological
Sciences, 4th Floor, Gakkai Center Bldg., 4-16, Yayoi 2-chome, Bunkyo-ku,
Tokyo 113, Japan) V.1- 1976- Volume(issue)/page/year: 5,141,1980
*** REVIEWS ***
TOXICOLOGY REVIEW
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag,
Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951-
Volume(issue)/page/year: 15,951,1965
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