Molecule

Limipterin

AlkaPlorer ID: AK535041

Synonym: None

IUPAC Name: N-[(2R,3R,4R,5S,6R)-2-[(1R,2S)-1-(2-amino-4-oxo-3H-pteridin-6-yl)-1-hydroxypropan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide

Structure

SMILES: CC(O)=N[C@H]1[C@H](O[C@@H](C)[C@H](O)C2=CN=C3NC(=N)N=C(O)C3=N2)O[C@H](CO)[C@@H](O)[C@@H]1O

InChI: InChI=1S/C17H24N6O8/c1-5(11(26)7-3-19-14-10(21-7)15(29)23-17(18)22-14)30-16-9(20-6(2)25)13(28)12(27)8(4-24)31-16/h3,5,8-9,11-13,16,24,26-28H,4H2,1-2H3,(H,20,25)(H3,18,19,22,23,29)/t5-,8+,9+,11-,12+,13+,16+/m0/s1

InChIKey: UFPLHRPHJDMHRW-GQQLITPASA-N

Reference

Pteridines. Part CVI. Isolation and characterization of limipterin (1‐O‐(<scp>L</scp>‐erythro‐biopterin‐2′‐yl)‐β‐N‐acetylglucosamine) and its 5,6,7,8‐tetrahydro derivative from green sulfur bacterium Chlorobium limicola f. thiosulfatophilum NCIB 8327

PubChem CID: 135424681

LOTUS: LTS0155485

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Chlorobium limicola	Chlorobium	Chlorobiaceae	Chlorobiales	Chlorobiia	Chlorobiota	None	Bacteria

Properties Information

Molecule Weight: 440.4130000000001

TPSA？: 230.51

MolLogP？: -2.2395299999999976

Number of H-Donors: 8

Number of H-Acceptors: 12

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi