Responsive image

Common name


(2S,3R)-2-(hydroxymethyl)tetrahydrofuran-3-ol

IUPAC name


(2S,3R)-2-(hydroxymethyl)tetrahydrofuran-3-ol

SMILES


O1CCC(C1CO)O

Common name


(2S,3R)-2-(hydroxymethyl)tetrahydrofuran-3-ol

IUPAC name


(2S,3R)-2-(hydroxymethyl)tetrahydrofuran-3-ol

SMILES


O1CCC(C1CO)O

INCHI


InChI=1S/C5H10O3/c6-3-5-4(7)1-2-8-5/h4-7H,1-3H2/t4-,5+/m1/s1

FORMULA


C5H10O3

Responsive image

Common name


(2S,3R)-2-(hydroxymethyl)tetrahydrofuran-3-ol

IUPAC name


(2S,3R)-2-(hydroxymethyl)tetrahydrofuran-3-ol





Molecular weight


118.131

clogP


0.099

clogS


0.528

Frequency


0.0003





HBond Acceptor


3

HBond Donor


2

Total Polar
Surface Area


49.69

Number of Rings


1

Rotatable Bond


1

Drug ID Common name Structure CAS Compound class Therapeutic area
FDBD01107 Telbivudine Responsive image Antiviral Agents; Nucleic Acid Synthesis Inhibitors; Antiinfectives for Systemic Use; Direct Acting Antivirals; Antivirals for Systemic Use; Nucleoside and Nucleotide Reverse Transcriptase Inhibitors; For the treatment of chronic hepatitis B in adult and adolescent patients
1 , 1
FRAGNAME PDBID SIMILIRITY XSCORE SMILE HAC
2py4_ligand_2_6.mol2 2py4 1 -6.37 C1C[C@@H]([C@H](O1)CO)O 8
3ehw_ligand_2_6.mol2 3ehw 1 -6.35 OC[C@@H]1[C@H](CCO1)O 8
2yay_ligand_2_6.mol2 2yay 1 -6.25 C1C[C@@H]([C@H](O1)CO)O 8
2yb0_ligand_1_1.mol2 2yb0 1 -6.25 C1C[C@@H]([C@H](O1)CO)O 8
4uxh_ligand_2_15.mol2 4uxh 1 -6.21 C([C@H]1OCC[C@@H]1O)O 8
2yaz_ligand_2_3.mol2 2yaz 1 -6.17 C(O)[C@@H]1[C@H](CCO1)O 8
1z34_ligand_1_0.mol2 1z34 1 -6.09 C(O)[C@H]1OCC[C@@H]1O 8
3ipx_ligand_1_1.mol2 3ipx 1 -6.07 C1O[C@@H]([C@H](C1)O)CO 8
4knz_ligand_2_5.mol2 4knz 1 -6.07 OC[C@@H]1[C@H](CCO1)O 8
2qch_ligand_2_3.mol2 2qch 1 -6.05 C(O)[C@@H]1[C@H](CCO1)O 8
171 , 18