UCSF

ZINC00895230

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
October 4th, 2005 12 Yes

Popular Name: Ureidosuccinic acid Ureidosuccinic acid

Find On: PubMed — Wikipedia — Google

CAS Numbers: 13184-27-5 , 16649-79-9 , 34879-34-0 , 923-37-5

Other Names:

(2S)-2-(carbamoylamino)butanedioic acid; CARBAMYUL-L-ASPARTATE; DL-Aspartic acid, N-(aminocarbonyl)-; N-(Aminocarbonyl)-DL-aspartic acid; N-Carbamoyl-DL-aspartic acid; N-Carbamoyl-L-Aspartate; Ureidosuccinic acid; bmse000453; carbamoyl-L-aspartate; carbam

13184-27-5; N-(aminocarbonyl)aspartic acid; nsc14983

16649-79-9; N-carbamoyl-L-aspartate; carbamoyl-aspartate; carbamyl-L-aspartate; carbamyl-aspartate; carbamyul-L-aspartate; carbamyul-aspartate

2-Ureidobutanedioate; 2-Ureidobutanedioic acid; Aspartic acid, N-carbamoyl-; Aspartic acid, N-carbamoyl-, L-; Carbamoylaspartic acid; Carbamyl-l-aspartic acid; Carbamylaspartic acid; L-Aspartic acid, N-(aminocarbonyl)-; L-n-carbamoylaspartic acid; L-ureid

2-Ureidobutanedioate; 2-Ureidobutanedioic acid; Carbamoylaspartic acid; Carbamyl-L-aspartic acid; Carbamylaspartic acid; L-N-Carbamoylaspartic acid; L-Ureidosuccinate; L-Ureidosuccinic acid; N-(Aminocarbonyl)-L-aspartic acid; N-Carbamoyl-L-aspartate; N-Ca

2-Ureidobutanedioate;2-Ureidobutanedioic acid;Carbamoylaspartic acid;Carbamyl-L-aspartic acid;Carbamylaspartic acid;L-N-Carbamoylaspartic acid;L-Ureidosuccinate;L-Ureidosuccinic acid;N-(Aminocarbonyl)-L-aspartic acid;N-Carbamoyl-L-aspartate;N-Carbamoyl-L-

2-Ureidobutanedioic acid; Carbamylaspartic acid; N-(Aminocarbonyl)-DL-aspartic acid; Ureidosuccinic acid

2-Ureidosuccinic acid

2-[(aminocarbonyl)amino]succinic acid

aspartic acid, N-(aminocarbonyl)-

Aspartic acid, N-carbamoyl-, calcium salt (1:1), DL-; Calcium DL-N-carbamoylaspartate; Calcium N-carbamoyl-DL-aspartate; Calcium N-carbamoyoaspartate DL-form; Calcium ureidosuccinate; DL-N-Carbamoylaspartic acid calcium salt; EINECS 250-383-5; LS-22082; P

C00438; N-Carbamoyl-L-aspartate

Carbaica

Carbamoyl-DL-Asp-OH

Carbamoyl-l-aspartic acid magnesium salt

Carbamyl-L-aspartic acid; L-ureidosuccinic acid; N-(aminocarbonyl)-L-aspartic acid; N-carbamoyl-S-aspartic acid; carbamyl-L-aspartic acid

CHEBI:12496; CHEBI:44316; CHEBI:7257; CHEBI:21688

MFCD00042822

MFCD01318844

MFCD01664828

N-(aminocarbonyl)aspartic acid

N-Carbamoyl-DL-aspartic acid

N-Carbamoyl-DL-aspartic acid, 98%

N-CarbaMoyl-DL-asparticAcid

N-Carbamoyl-L-Aspartate

N-carbamoyl-L-aspartic acid

N-carbamoylaspartic acid

Store at 2-8°C

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) -3.33 -4.2 -110.1 3 7 -2 135 174.112 4 ↓

Vendor Notes

Note Type Comments Provided By
ALOGPS_SOLUBILITY 2.13e+01 g/l DrugBank-experimental
purity 9.500000000000000e+001 Enamine Building Blocks Enamine Building Blocks
Purity 95% Fluorochem
Melting_Point ca 175? dec. Alfa-Aesar
Melting_Point ca 175° dec. Alfa-Aesar
UniProt Database Links PYR1_DICDI; PYR1_DROME; PYR1_EMENI; PYR1_HUMAN; PYR1_MESAU; PYR1_MOUSE; PYR1_SCHPO; PYR1_SQUAC; PYR1_YEAST; PYRB1_PEA; PYRB1_SHEHH; PYRB2_PEA; PYRB2_SHEHH; PYRB3_PEA; PYRB3_SHEHH; PYRB_ACAM1; PYRB_ACIAC; PYRB_ACIAD; PYRB_ACIB3; PYRB_ACIB5; PYRB_ACIBC; PYR ChEBI
Reactome Database Links REACT_1965; REACT_744 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
De novo synthesis of UMP
Pyrimidine biosynthesis

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