Thiomuracin G
AlkaPlorer ID: AK067378
Synonym: None
IUPAC Name: 2-[[1-hydroxy-2-[[hydroxy-[2-[(18S,25S,32S,35S)-16,23,30,33-tetrahydroxy-18-(2-hydroxy-2-iminoethyl)-35-[(2R)-4-hydroxy-3-oxobutan-2-yl]-25-[(R)-hydroxy(phenyl)methyl]-32-[(4-hydroxyphenyl)methyl]-21-methyl-3,13,20,27,37-pentathia-7,17,24,31,34,39,40,41,42,43-decazaheptacyclo[34.2.1.12,5.112,15.119,22.126,29.06,11]tritetraconta-1(38),2(43),4,6(11),7,9,12(42),14,16,19(41),21,23,26(40),28,30,33,36(39)-heptadecaen-8-yl]-1,3-thiazol-4-yl]methylidene]amino]prop-2-enylidene]amino]prop-2-enoic acid
Structure
SMILES: C=C(N=C(O)C(=C)N=C(O)C1=CSC(C2=CC=C3C4=NC(=CS4)C(O)=N[C@@H](CC(=N)O)C4=NC(=C(C)S4)C(O)=N[C@@H]([C@H](O)C4=CC=CC=C4)C4=NC(=CS4)C(O)=N[C@@H](CC4=CC=C(O)C=C4)C(O)=N[C@@H]([C@@H](C)C(=O)CO)C4=NC(=CS4)C4=NC(=CS4)C3=N2)=N1)C(=O)O
InChI: InChI=1S/C59H50N14O13S6/c1-24(40(76)18-74)42-57-70-39(23-91-57)55-66-35(19-88-55)44-31(14-15-32(63-44)54-68-36(21-89-54)49(81)61-25(2)47(79)62-26(3)59(85)86)53-67-37(20-87-53)51(83)65-34(17-41(60)77)56-73-43(27(4)92-56)52(84)72-45(46(78)29-8-6-5-7-9-29)58-69-38(22-90-58)50(82)64-33(48(80)71-42)16-28-10-12-30(75)13-11-28/h5-15,19-24,33-34,42,45-46,74-75,78H,2-3,16-18H2,1,4H3,(H2,60,77)(H,61,81)(H,62,79)(H,64,82)(H,65,83)(H,71,80)(H,72,84)(H,85,86)/t24-,33-,34-,42-,45-,46+/m0/s1
InChIKey: MBPATICGTRJTMR-PWKTXWFVSA-N
Reference
Ribosomally Synthesized Thiopeptide Antibiotics Targeting Elongation Factor Tu
PubChem CID: 42637201
LOTUS: LTS0060497
{NPAtlas: NPA005245
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Nonomuraea sp. | Nonomuraea | Streptosporangiaceae | Streptosporangiales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 1355.5360000000005
TPSA？: 444.91
MolLogP？: 10.75109
Number of H-Donors: 12
Number of H-Acceptors: 25
RingCount: 10
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|