about
Structure-Based Drug Design and Optimization of Mannoside Bacterial FimH AntagonistsProtection against Escherichia coli-induced urinary tract infections with hybridoma antibodies directed against type 1 fimbriae or complementary D-mannose receptorsToxic isolectins from the mushroom Boletus venenatus.Attachment of Pasteuria penetrans Endospores to the Surface of Meloidogyne javanica Second-stage Juveniles.Trityl-derivatized carbohydrates immobilized on a polystyrene microplate.Novel lectins from rhizomes of two Acorus species with mitogenic activity and inhibitory potential towards murine cancer cell lines.Phenylthiomethyl glycosides: convenient synthons for the formation of azidomethyl and glycosylmethyl glycosides and their derivatives.Macoma birmanica agglutinin recognizes glycoside clusters of beta-GlcNAc/Glc and alpha-Man.Isolation of a lectin and a galactoxyloglucan from Mucuna sloanei seeds.Insecticidal and antifungal activity of a protein from Pouteria torta seeds with lectin-like properties.Transcription factor NFIC undergoes N-glycosylation during early mammary gland involution.Rational design of novel glycomimetics: inhibitors of concanavalin A.The activation of cloned macrophages by concanavalin A for tumoricidal effect: assessment of tumor cell cytotoxicity by a clonogenic assayIdentification of a 148-kDa surface lectin from Giardia lamblia with specificity for alpha-methyl-D-mannoside
P921
Q27661999-F1F8C80B-3453-420B-AE14-3978D0464997Q28360014-1577FB34-4F22-4829-BE36-E50BB1705A74Q33526120-B470E71F-9BB4-4EB8-BFE3-AEC1F6A1DF76Q37049059-672F9478-85AF-4564-AC83-1DE7241EB534Q38360471-486ACB15-FD41-4811-99B7-B1E2883B127DQ40410312-C993FBBC-41DE-425A-B90F-FAD9A84EEA2CQ42000174-C37C01FA-8BA4-448D-A69C-DA7B4A144C65Q43257417-ADB472CE-2F05-4905-9AB5-8646E25331A6Q43270817-4FFE7CA2-998C-4031-8B31-1A89BB2420A4Q43420729-CD142AD1-54A1-4E22-B6CD-4608FE449E37Q43980975-4A463032-D05C-4117-9F44-F3851AB1130BQ46259576-77768802-42C0-40FC-A124-1B73E7980A58Q70312488-BEC38E15-C9B9-49E0-AF44-CD69CE14020CQ70983888-C2EF4A92-5E11-4624-BC55-E27AF67B1A99
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Methyl alpha-D-mannoside
@en
type
label
Methyl alpha-D-mannoside
@en
altLabel
1-O-Methyl-alpha-D-mannopyranoside
@en
alpha-Methyl mannopyranoside
@en
alpha-methyl-D-mannoside
@en
prefLabel
Methyl alpha-D-mannoside
@en
P638
P592
P661
P662
P683
P1579
P2017
CO[C@@H]1[C@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
P2067
P231
25281-48-5
P233
COC1C(C(C(C(O1)CO)O)O)O
P234
1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
P235
HOVAGTYPODGVJG-VEIUFWFVSA-N
P274
P3117
DTXSID10897266
P4168
P592
CHEMBL195368