Halomicin A
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Category | Antibiotics |
Catalog number | BBF-01309 |
CAS | 56411-51-9 |
Molecular Weight | 810.93 |
Molecular Formula | C43H58N2O13 |
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Description
It is produced by the strain of Micromonospora halophytica var. nigra. It's an ansamycin antibiotic. Halomicin complex has activity against gram-positive and gram-negative bacteria (individual).
Specification
Synonyms | SP-30-A; 4-Deoxy-4-[3-hydroxy-2-(1-hydroxyethyl)-1-pyrrolidinyl]rifamycin; Rifamycin, 4-deoxy-4-(3-hydroxy-2-(1-hydroxyethyl)-1-pyrrolidinyl)- |
IUPAC Name | [(7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,15,17,29-tetrahydroxy-27-[3-hydroxy-2-(1-hydroxyethyl)pyrrolidin-1-yl]-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23-dioxo-8,30-dioxa-24-azatetracyclo[23.3.1.14,7.05,28]triaconta-1(29),2,4,9,19,21,25,27-octaen-13-yl] acetate |
Canonical SMILES | CC1C=CC=C(C(=O)NC2=CC(=C3C(=C2O)C(=C(C4=C3C(=O)C(O4)(OC=CC(C(C(C(C(C(C1O)C)O)C)OC(=O)C)C)OC)C)C)O)N5CCC(C5C(C)O)O)C |
InChI | InChI=1S/C43H58N2O13/c1-19-12-11-13-20(2)42(54)44-27-18-28(45-16-14-29(48)34(45)25(7)46)31-32(38(27)52)37(51)24(6)40-33(31)41(53)43(9,58-40)56-17-15-30(55-10)21(3)39(57-26(8)47)23(5)36(50)22(4)35(19)49/h11-13,15,17-19,21-23,25,29-30,34-36,39,46,48-52H,14,16H2,1-10H3,(H,44,54)/b12-11-,17-15-,20-13-/t19-,21+,22+,23+,25?,29?,30-,34?,35-,36+,39+,43-/m0/s1 |
InChI Key | QKZDEAZSGKLVSB-JHZNXVQTSA-N |
Properties
Appearance | Yellow Crystal |
Antibiotic Activity Spectrum | Gram-positive bacteria; Gram-negative bacteria |
Boiling Point | 953.7 °C at 760 mmHg |
Melting Point | 192-194 °C |
Density | 1.35 g/cm3 |
Solubility | Soluble in Benzene, Dioxane |
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳