Glycocyamine
PubChem CID: 763
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| Compound Synonyms | glycocyamine, guanidinoacetic acid, 352-97-6, Guanidineacetic acid, 2-Guanidinoacetic acid, Guanidoacetic acid, N-amidinoglycine, Betacyamine, Guanyl glycine, guanidinoacetate, Betasyamine, Glykocyamin, Guanidylacetic acid, GLYCINE, N-AMIDINO-, Guanidine, (carboxymethyl)-, glycine, N-(aminoiminomethyl)-, N-(Aminoiminomethyl)glycine, N-[AMINO(IMINO)METHYL]GLYCINE, n-amidino-glycine, amidinoglycine, N-carbamimidoylglycine, Acetic acid, ((aminoiminomethyl)amino)-, 2-(diaminomethylideneamino)acetic acid, N-(carbamimidoyl)glycine, (carbamimidamido)acetic acid, 2-carbamimidamidoacetic acid, NSC 1901, Guanidoacetate, Guanidylacetate, GUANIDINO ACETATE, Guanidineacetate, a-Guanidinoacetate, b-Guanidinoacetate, EINECS 206-529-5, MFCD00004278, N-(aminoiminomethyl)-glycine, beta-Guanidinoacetate, GO52O1A04E, alpha-Guanidinoacetate, a-Guanidinoacetic acid, b-Guanidinoacetic acid, CHEBI:16344, AI3-17119, NSC1901, beta-Guanidinoacetic acid, NSC-1901, (carboxymethyl)-Guanidine, alpha-Guanidinoacetic acid, GLYCOCYAMINE [MI], NSC-26360, NSC-227847, .alpha.-Guanidinoacetic acid, GLYCOCYAMINE [WHO-DD], CHEMBL281593, [(aminoiminomethyl)amino]-Acetate, DTXSID50861885, [(aminoiminomethyl)amino]-Acetic acid, 2-[[Amino(imino)methyl]amino]acetate, 2-[[Amino(imino)methyl]amino]acetic acid, 2-((AMINO(IMINO)METHYL)AMINO)ACETIC ACID, NMG, N-(Amino(Imino)Methyl)Glycine, ((aminoiminomethyl)amino)-Acetate, N-Guanylglycine, ((aminoiminomethyl)amino)-Acetic acid, 2-((Amino(imino)methyl)amino)acetate, Acetic acid, [(aminoiminomethyl)amino]-, CHEBI:131444, UNII-GO52O1A04E, Glucocyamine, guanidine acetic acid, GUANIDOACETIC_ACID, bmse000384, Guanidineacetic acid, 99%, Glycine, N-amidino-(8CI), SCHEMBL33970, 2-carbamimidamido-acetic acid, AMIDINOGLYCINE [INCI], Glycine, N-amidino- (8CI), GTPL5325, (Diaminomethylenamino)-essigsaure, DTXCID70810739, HMS3604I10, GAA, Glycocyamine, Guanidinoacetate, NSC26360, AC2229, BDBM50021601, NSC227847, s6340, STL164350, AKOS005363765, DB02751, FG23711, HY-W021448, 2-[(diaminomethylidene)amino]acetic acid, ([Amino(imino)methyl]amino)acetic acid #, AS-10760, SY015122, DB-069193, CS-0040590, G0167, NS00009387, EN300-49151, C00581, Q2740979, Z586248684, N-(Aminoiminomethyl)-glycine, 2-[[Amino(imino)methyl]amino]acetic acid, NSC 26360, 206-529-5 |
|---|---|
| Ghose Rule | False |
| Classyfire Kingdom | Organic compounds |
| Topological Polar Surface Area | 102.0 |
| Hydrogen Bond Donor Count | 3.0 |
| Pfizer 3 75 Rule | True |
| Np Classifier Class | Aminoacids |
| Deep Smiles | OC=O)CN=CN)N |
| Heavy Atom Count | 8.0 |
| Classyfire Class | Carboxylic acids and derivatives |
| Description | Guanidino acetic acid, also known as guanidinoacetate or glycocyamine, belongs to alpha amino acids and derivatives class of compounds. Those are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. Guanidino acetic acid is slightly soluble (in water) and a weakly acidic compound (based on its pKa). Guanidino acetic acid can be found in apple and loquat, which makes guanidino acetic acid a potential biomarker for the consumption of these food products. Guanidino acetic acid can be found primarily in most biofluids, including cellular cytoplasm, feces, urine, and cerebrospinal fluid (CSF), as well as in human brain, kidney and liver tissues. In humans, guanidino acetic acid is involved in a couple of metabolic pathways, which include arginine and proline metabolism and glycine and serine metabolism. Guanidino acetic acid is also involved in several metabolic disorders, some of which include dihydropyrimidine dehydrogenase deficiency (DHPD), hyperprolinemia type II, prolinemia type II, and hyperornithinemia-hyperammonemia-homocitrullinuria [hhh-syndrome]. Moreover, guanidino acetic acid is found to be associated with chronic renal failure and schizophrenia. Guanidino acetic acid is a non-carcinogenic (not listed by IARC) potentially toxic compound. Chronic Exposure: Kidney dialysis is usually needed to relieve the symptoms of uremic syndrome until normal kidney function can be restored. |
| Classyfire Subclass | Amino acids, peptides, and analogues |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 116.0 |
| Database Name | fooddb_chem_all;hmdb_chem_all;imppat_phytochem;pubchem |
| Defined Atom Stereocenter Count | 0.0 |
| Uniprot Id | Q14353, P50440 |
| Iupac Name | 2-(diaminomethylideneamino)acetic acid |
| Class | Carboxylic acids and derivatives |
| Veber Rule | True |
| Classyfire Superclass | Organic acids and derivatives |
| Xlogp | -1.6 |
| Superclass | Organic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Gsk 4 400 Rule | True |
| Molecular Formula | C3H7N3O2 |
| Inchi Key | BPMFZUMJYQTVII-UHFFFAOYSA-N |
| Silicos It Class | Soluble |
| Rotatable Bond Count | 2.0 |
| State | Solid |
| Synonyms | Glycocyamine, Guanidinoacetate, N-(Carbamimidoyl)glycine, N-[Amino(imino)methyl]glycine, N-Amidinoglycine, Guanidinoacetic acid, Guanidoacetate, (Carboxymethyl)-guanidine, 2-[[Amino(imino)methyl]amino]acetate, 2-[[Amino(imino)methyl]amino]acetic acid, a-Guanidinoacetate, a-Guanidinoacetic acid, alpha-Guanidinoacetate, alpha-Guanidinoacetic acid, b-Guanidinoacetate, b-Guanidinoacetic acid, beta-Guanidinoacetate, beta-Guanidinoacetic acid, Betacyamine, Betasyamine, Guanidineacetate, Guanidineacetic acid, Guanidylacetate, Guanidylacetic acid, Guanyl glycine, N-Amidino-glycine, [(Aminoiminomethyl)amino]-acetate, [(Aminoiminomethyl)amino]-acetic acid, Glycocyamine, 2-(14)C-labeled, Glycocyamine, ion (1-), Glycocyamine monohydrochloride, guanidinoacetic acid |
| Esol Class | Highly soluble |
| Functional Groups | CC(=O)O, CN=C(N)N |
| Compound Name | Glycocyamine |
| Kingdom | Organic compounds |
| Exact Mass | 117.054 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 117.054 |
| Hydrogen Bond Acceptor Count | 3.0 |
| Molecular Weight | 117.11 |
| Gi Absorption | True |
| Covalent Unit Count | 1.0 |
| Total Atom Stereocenter Count | 0.0 |
| Total Bond Stereocenter Count | 0.0 |
| Molecular Framework | Aliphatic acyclic compounds |
| Lipinski Rule Of 5 | True |
| Inchi | InChI=1S/C3H7N3O2/c4-3(5)6-1-2(7)8/h1H2,(H,7,8)(H4,4,5,6) |
| Smiles | C(C(=O)O)N=C(N)N |
| Np Classifier Biosynthetic Pathway | Amino acids and Peptides |
| Defined Bond Stereocenter Count | 0.0 |
| Egan Rule | False |
| Taxonomy Direct Parent | Alpha amino acids and derivatives |
| Np Classifier Superclass | Small peptides |
- 1. Outgoing r'ship
FOUND_INto/from Diospyros Melanoxylon (Plant) Rel Props:Reference:ISBN:9788172361150 - 2. Outgoing r'ship
FOUND_INto/from Eriobotrya Japonica (Plant) Rel Props:Source_db:fooddb_chem_all - 3. Outgoing r'ship
FOUND_INto/from Malus Domestica (Plant) Rel Props:Source_db:fooddb_chem_all