UCSF

ZINC00895314

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
November 26th, 2005 8 Yes

Popular Name: Glycocyamine Glycocyamine

Find On: PubMed — Wikipedia — Google

CAS Numbers: 14901-20-3 , 352-97-6 , [14901-20-3] , [352-97-6]

Other Names:

"Guanidineacetic acid, 99%"

(carboxymethyl)-Guanidine; 2-[[Amino(imino)methyl]amino]acetate; 2-[[Amino(imino)methyl]amino]acetic acid; Betacyamine; Betasyamine; Glycocyamine; Guanidineacetate; Guanidineacetic acid; Guanidinoacetate; Guanidinoacetic acid; Guanidoacetate; Guanidoaceti

(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-Guanidinoace

(carboxymethyl)-Guanidine;2-[[Amino(imino)methyl]amino]acetate;2-[[Amino(imino)methyl]amino]acetic acid;Betacyamine;Betasyamine;Glycocyamine;Guanidineacetate;Guanidineacetic acid;Guanidinoacetate;Guanidinoacetic acid;Guanidoacetate;Guanidoacetic acid;Guan

2-carbamimidamidoacetic acid

2-carbamimidamidoacetic acid hydrochloride

2-Guanidinoacetic acid

352-97-6; C00581; Glycocyamine; Guanidinoacetate; Guanidinoacetic acid; Guanidoacetic acid; N-Amidinoglycine

352-97-6; GUANIDOACETIC_ACID; N-amidinoglycine; glycocyamine; guanidinoacetate; guanidinoacetic acid

AI3-17119; Acetic acid, ((aminoiminomethyl)amino)-; Betacyamine; Betasyamine; C3H7N3O2; EINECS 206-529-5; GLYCINE, N-AMIDINO-; GLYCOCYAMINE; Glykocyamin; Guanidine, (carboxymethyl)-; Guanidineacetic acid; Guanidinoacetic acid; Guanidylacetic acid; Guanyl

CHEBI:44474; CHEBI:5560; CHEBI:24440; CHEBI:14369

Glycocyamine; N-(carbamimidoyl)glycine; N-[Amino(Imino)Methyl]Glycine

Guanidineacetic acid

Guanidineacetic acid, 99+%

guanidinoacetate

guanidinoacetic acid

guanidinoacetic acid zwitterion

GuanidinoaceticAcid

Guanidinooacetic Acid

Guanidoacetic acid

MFCD00004278

MFCD09800614

N-Amidinoglycine

N-carbamimidoylglycine

N-[Amino(Imino)Methyl]Glycine

N/A

QA-9591

{[Amino(imino)methyl]amino}-acetic acid hydrochloride

Download: MOL2 SDF SMILES Flexibase

Annotations

Vendors

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) -2.49 -4.02 -43.56 5 5 0 103 117.108 3 ↓

Vendor Notes

Note Type Comments Provided By
MP 298 - 300 Enamine Building Blocks
MP 298...300 Enamine Building Blocks
ALOGPS_SOLUBILITY 4.19e+00 g/l DrugBank-experimental
purity 9.500000000000000e+001 Enamine Building Blocks Enamine Building Blocks
Melting_Point ca 280? dec. Alfa-Aesar
Melting_Point ca 280° dec. Alfa-Aesar
UniProt Database Links GAMTA_XENLA; GAMTB_XENLA; GAMT_BOVIN; GAMT_DANRE; GAMT_HUMAN; GAMT_MOUSE; GAMT_RAT; GAMT_XENTR; GATM_BOVIN; GATM_CHICK; GATM_DANRE; GATM_HUMAN; GATM_MACFA; GATM_MOUSE; GATM_PIG; GATM_PONAB; GATM_RAT; GATM_XENLA; GATM_XENTR ChEBI
Reactome Database Links REACT_2094; REACT_396 ChEBI

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
Z104301-2-O GABA-A Receptor; Anion Channel (cluster #2 Of 8), Other Other 2100 0.99 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
Z104301 Z104301 GABA-A Receptor; Anion Channel 2100 0.99 Binding ≤ 10μM

Direct Reactome Annotations (via ChEBI)

Description Species
Creatine metabolism

Analogs ( Draw Identity 99% 90% 80% 70% )