Stem definition | Drug id | CAS RN |
---|---|---|
4624 | 103-82-2 |
None
None
Date | Agency | Company | Orphan |
---|---|---|---|
Dec. 23, 1987 | FDA | B BRAUN |
None
None
None
None
Source | Code | Description |
---|---|---|
ATC | A16AX30 | ALIMENTARY TRACT AND METABOLISM OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS Various alimentary tract and metabolism products |
MeSH PA | D000963 | Antimetabolites |
MeSH PA | D000964 | Antimetabolites, Antineoplastic |
MeSH PA | D000970 | Antineoplastic Agents |
MeSH PA | D009676 | Noxae |
FDA MoA | N0000175806 | Ammonium Ion Binding Activity |
FDA EPC | N0000175807 | Nitrogen Binding Agent |
CHEBI has role | CHEBI:22676 | auxins |
CHEBI has role | CHEBI:27026 | toxins |
CHEBI has role | CHEBI:35219 | plant growth inhibitors |
CHEBI has role | CHEBI:50904 | alergeno |
CHEBI has role | CHEBI:75772 | S. cerevisiae metabolites |
CHEBI has role | CHEBI:76924 | plant metabolites |
CHEBI has role | CHEBI:76956 | Aspergillus metabolites |
CHEBI has role | CHEBI:76971 | Escherichia coli metabolites |
CHEBI has role | CHEBI:77746 | Homo sapiens metabolite |
CHEBI has role | CHEBI:90318 | EC 6.4.1.1 (pyruvate carboxylase) inhibitors |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Hyperammonemia | indication | 9360008 | |
Hypokalemia | contraindication | 43339004 | |
Body fluid retention | contraindication | 43498006 | |
Chronic heart failure | contraindication | 48447003 | |
Acute nephropathy | contraindication | 58574008 | |
Metabolic acidosis | contraindication | 59455009 | |
Hyperglycemia | contraindication | 80394007 | DOID:4195 |
Kidney disease | contraindication | 90708001 | DOID:557 |
Seizure disorder | contraindication | 128613002 | |
Disease of liver | contraindication | 235856003 | DOID:409 |
Edema | contraindication | 267038008 | |
CNS Toxicity | contraindication |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 4.37 | acidic |
None
None
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
Aldose reductase | Enzyme | IC50 | 4.02 | CHEMBL |
ID | Source |
---|---|
D05867 | KEGG_DRUG |
114-70-5 | SECONDARY_CAS_RN |
4019576 | VANDF |
CHEBI:30745 | CHEBI |
CHEMBL1044 | ChEMBL_ID |
CHEMBL1200358 | ChEMBL_ID |
C025136 | MESH_SUPPLEMENTAL_RECORD_UI |
DB09269 | DRUGBANK_ID |
ER5I1W795A | UNII |
33332 | RXNORM |
19292 | MMSL |
d05460 | MMSL |
001244 | NDDF |
004954 | NDDF |
125705007 | SNOMEDCT_US |
398818001 | SNOMEDCT_US |
C0070620 | UMLSCUI |
PAC | PDB_CHEM_ID |
999 | PUBCHEM_CID |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
Ammonul | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0187-0010 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | NDA | 26 sections |
SODIUM PHENYLACETATE and SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 13811-705 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
Ammonul | HUMAN PRESCRIPTION DRUG LABEL | 2 | 62592-720 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | NDA | 28 sections |
Sodium Phenylacetate and Sodium Benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 67457-844 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 27 sections |
SODIUM PHENYLACETATE AND SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 68382-396 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 24 sections |
SODIUM PHENYLACETATE AND SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 68382-396 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 24 sections |
Sodium Phenylacetate and sodium benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 68475-001 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 24 sections |
Sodium Phenylacetate and sodium benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 68475-001 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 24 sections |
SODIUM PHENYLACETATE AND SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 68682-001 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | NDA authorized generic | 26 sections |
SODIUM PHENYLACETATE and SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 69784-810 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
SODIUM PHENYLACETATE and SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 69784-810 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
SODIUM PHENYLACETATE and SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 69784-811 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
SODIUM PHENYLACETATE and SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 69784-811 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
SODIUM PHENYLACETATE AND SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 70511-101 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
SODIUM PHENYLACETATE AND SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 70511-101 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
Sodium Phenylacetate and Sodium Benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 70511-102 | INJECTION | 100 mg | INTRAVENOUS | NDA | 29 sections |
Sodium Phenylacetate and Sodium Benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 70511-102 | INJECTION | 100 mg | INTRAVENOUS | NDA | 29 sections |
SODIUM PHENYLACETATE and SODIUM BENZOATE | HUMAN PRESCRIPTION DRUG LABEL | 2 | 70556-100 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 28 sections |
Sodium Phenylacetate and Sodium Benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 72266-236 | INJECTION | 100 mg | INTRAVENOUS | NDA | 29 sections |
Sodium Phenylacetate and Sodium Benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 72266-247 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 27 sections |
Sodium Phenylacetate and Sodium Benzoate | HUMAN PRESCRIPTION DRUG LABEL | 2 | 72266-247 | INJECTION, SOLUTION, CONCENTRATE | 100 mg | INTRAVENOUS | ANDA | 27 sections |