Item 1 of 1 (back to results) L-aspartic acid 4-semialdehyde betaine The betaine obtained by transfer of a proton from the carboxylic acid group to the amino group of L-aspartic acid 4-semialdehyde.

Current search: 04. Bioactive Capabilities of Specific Chemicals : Oxidoreductases [EC:1] > Acting on the CH-OH group of donors [EC:1.1] > With NAD or NADP as acceptor [EC:1.1.1] > Homoserine dehydrogenase [EC:1.1.1.3] > L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] × Select any link to see items in a related category. more general categories    information about this item 04. Bioactive Capabilities of Specific Chemicals   04. Bioactive Capabilities of Specific Chemicals  Oxidoreductases [EC:1] (1697)   Acting on the CH-OH group of donors [EC:1.1] (576)   With NAD or NADP as acceptor [EC:1.1.1] (507)   Homoserine dehydrogenase [EC:1.1.1.3] (7)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  Acting on the aldehyde or oxo group of donors [EC:1.2] (133)   With NAD or NADP as acceptor [EC:1.2.1] (114)   Aspartate-semialdehyde dehydrogenase [EC:1.2.1.11] (5)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  Acting on the CH-NH group of donors [EC:1.5] (120)   With NAD or NADP as acceptor [EC:1.5.1] (77)   Carboxynorspermidine synthase [EC:1.5.1.43] (9)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  Transferases [EC:2] (1441)   Transferring aldehyde or ketonic groups [EC:2.2] (35)   Transketolases and Transaldolases [EC:2.2.1] (35)   2-amino-3,7-dideoxy-D-threo-hept-6-ulosonate synthase [EC:2.2.1.10] (4)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  Transferring nitrogenous groups [EC:2.6] (152)   Transaminases [EC:2.6.1] (146)   Diaminobutyrate--pyruvate transaminase [EC:2.6.1.46] (4)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  Diaminobutyrate--2-oxoglutarate transaminase [EC:2.6.1.76] (4)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  Lyases [EC:4] (743)   Carbon-carbon lyases [EC:4.1] (299)   Aldehyde-Lyases [EC:4.1.2] (89)   2-amino-4,5-dihydroxy-6-oxo-7-(phosphonooxy)heptanoate synthase [EC:4.1.2.n6] (3)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  Carbon-nitrogen lyases [EC:4.3] (80)   Amine-Lyases [EC:4.3.3] (24)   4-hydroxy-tetrahydrodipicolinate synthase [EC:4.3.3.7] (5)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1) 08. Chemical Category  08. Chemical Category  main group molecular entity [CHEBI:33579] (25650)   p-block molecular entity [CHEBI:33675] (25343)   pnictogen molecular entity [CHEBI:33302] (10027)   nitrogen molecular entity [CHEBI:51143] (7930)   quaternary nitrogen compound [CHEBI:26469] (238)   ammonium betaine [CHEBI:35284] (165)   amino-acid betaine [CHEBI:22860] (12)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  carbon group molecular entity [CHEBI:33582] (23847)   organic molecular entity [CHEBI:50860] (23769)   organic molecule [CHEBI:72695] (11399)   dipolar compound [CHEBI:51151] (494)   zwitterion [CHEBI:27369] (494)   onium betaine [CHEBI:35281] (213)   ammonium betaine [CHEBI:35284] (165)   amino-acid betaine [CHEBI:22860] (12)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1)  polyatomic entity [CHEBI:36357] (18777)   molecule [CHEBI:25367] (11520)   organic molecule [CHEBI:72695] (11399)   dipolar compound [CHEBI:51151] (494)   zwitterion [CHEBI:27369] (494)   onium betaine [CHEBI:35281] (213)   ammonium betaine [CHEBI:35284] (165)   amino-acid betaine [CHEBI:22860] (12)   L-aspartic acid 4-semialdehyde betaine [CHEBI:537519] (1) ChEBI Compound Accession Identifier:   [CHEBI:537519] ChEBI Compound Description:   The betaine obtained by transfer of a proton from the carboxylic acid group to the amino group of L-aspartic acid 4-semialdehyde. ChEBI Compound Identification Number:   537519 ChEBI InChI Value:   InChI=1S/C4H7NO3/c5-3(1-2-6)4(7)8/h2-3H,1,5H2,(H,7,8)/t3-/m0/s1 ChEBI InChIKey Value:   HOSWPDPVFBCLSY-VKHMYHEASA-N ChEBI Compound Name:   L-aspartic acid 4-semialdehyde betaine ChEBI SMILES Value:   [H]C(=O)C[C@H]([NH3+])C([O-])=O ChEBI Substance ID:   87351750 ChEBI URL:   ChEBI:537519 ChemSpider ID:   0 Ontomatica Chemical Accession Key (OnChAKey):   HOSWPDPVFBCLSY_VKHMYHEASA_N_000_000001 PubChem Compound ID:   5287708