| Stem definition | Drug id | CAS RN |
|---|---|---|
| beta-lactamase inhibitors | 2492 | 68373-14-8 |
| Dose | Unit | Route |
|---|---|---|
| 1 | g | P |
| Property | Value | Reference |
|---|---|---|
| MRTD (Maximum Recommended Therapeutic Daily Dose) | 285.97 ยตM/kg/day | Contrera JF, Matthews EJ, Kruhlak NL, Benz RD |
| Vd (Volume of distribution) | 0.32 L/kg | Lombardo F, Berellini G, Obach RS |
| CL (Clearance) | 5.10 mL/min/kg | Lombardo F, Berellini G, Obach RS |
| fu (Fraction unbound in plasma) | 0.62 % | Lombardo F, Berellini G, Obach RS |
| t_half (Half-life) | 1.10 hours | Lombardo F, Berellini G, Obach RS |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| Dec. 31, 1986 | FDA | PFIZER |
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Enterocolitis haemorrhagic | 68.55 | 26.81 | 14 | 1665 | 1452 | 63485891 |
| Hepatic function abnormal | 53.84 | 26.81 | 24 | 1655 | 37118 | 63450225 |
| Culture stool positive | 40.45 | 26.81 | 7 | 1672 | 295 | 63487048 |
| Stevens-Johnson syndrome | 32.58 | 26.81 | 15 | 1664 | 24935 | 63462408 |
| Toxic epidermal necrolysis | 32.36 | 26.81 | 15 | 1664 | 25319 | 63462024 |
| Klebsiella infection | 31.97 | 26.81 | 11 | 1668 | 8555 | 63478788 |
| Epidermolysis | 28.90 | 26.81 | 6 | 1673 | 673 | 63486670 |
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Cardiac septal defect | 66.43 | 21.44 | 12 | 1904 | 307 | 34954708 |
| Kidney duplex | 63.48 | 21.44 | 12 | 1904 | 396 | 34954619 |
| Enterocolitis haemorrhagic | 42.32 | 21.44 | 10 | 1906 | 973 | 34954042 |
| Hepatic function abnormal | 40.59 | 21.44 | 27 | 1889 | 44336 | 34910679 |
| Interstitial lung disease | 25.37 | 21.44 | 24 | 1892 | 65258 | 34889757 |
| Aspartate aminotransferase increased | 24.60 | 21.44 | 24 | 1892 | 67759 | 34887256 |
| Pyrexia | 23.16 | 21.44 | 54 | 1862 | 332959 | 34622056 |
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Enterocolitis haemorrhagic | 106.93 | 22.18 | 23 | 2942 | 2171 | 79739252 |
| Hepatic function abnormal | 70.51 | 22.18 | 40 | 2925 | 73067 | 79668356 |
| Culture stool positive | 44.73 | 22.18 | 9 | 2956 | 612 | 79740811 |
| Aspartate aminotransferase increased | 37.35 | 22.18 | 35 | 2930 | 138606 | 79602817 |
| Toxic epidermal necrolysis | 31.52 | 22.18 | 20 | 2945 | 44561 | 79696862 |
| Stevens-Johnson syndrome | 31.31 | 22.18 | 19 | 2946 | 39147 | 79702276 |
| Rash | 27.61 | 22.18 | 64 | 2901 | 578294 | 79163129 |
| Alanine aminotransferase increased | 27.49 | 22.18 | 32 | 2933 | 162538 | 79578885 |
| Interstitial lung disease | 25.75 | 22.18 | 26 | 2939 | 112574 | 79628849 |
| Klebsiella infection | 24.87 | 22.18 | 12 | 2953 | 15708 | 79725715 |
| Epidermolysis | 24.74 | 22.18 | 6 | 2959 | 962 | 79740461 |
| Pneumonia | 24.12 | 22.18 | 66 | 2899 | 660180 | 79081243 |
| Liver disorder | 22.85 | 22.18 | 20 | 2945 | 72397 | 79669026 |
| Clostridium colitis | 22.47 | 22.18 | 7 | 2958 | 2832 | 79738591 |
None
| Source | Code | Description |
|---|---|---|
| ATC | J01CG01 | ANTIINFECTIVES FOR SYSTEMIC USE ANTIBACTERIALS FOR SYSTEMIC USE BETA-LACTAM ANTIBACTERIALS, PENICILLINS Beta-lactamase inhibitors |
| FDA MoA | N0000000202 | beta Lactamase Inhibitors |
| MeSH PA | D000900 | Anti-Bacterial Agents |
| MeSH PA | D000890 | Anti-Infective Agents |
| MeSH PA | D065093 | beta-Lactamase Inhibitors |
| MeSH PA | D004791 | Enzyme Inhibitors |
| FDA EPC | N0000175930 | beta Lactamase Inhibitor |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Infection of skin AND/OR subcutaneous tissue | indication | 19824006 | |
| Infection due to Escherichia coli | indication | 71057007 | |
| Rhinoscleroma | indication | 72409005 | DOID:11336 |
| Cholangitis | indication | 82403002 | DOID:9446 |
| Female genital tract infection | indication | 125585007 | |
| Infectious disease of abdomen | indication | 128070006 | |
| Infection due to Enterobacteriaceae | indication | 128945009 | |
| Bacterial peritonitis | indication | 197171003 | |
| Infection due to Staphylococcus aureus | indication | 406602003 | |
| Ventilator-associated bacterial pneumonia caused by acinetobacter baumannii-calcoaceticus complex | indication | 429271009 | |
| Infection caused by carbapenem-resistant acinetobacter baumannii-calcoaceticus complex | indication | 445780006 | |
| Hospital-acquired bacterial pneumonia caused by acinetobacter baumannii-calcoaceticus complex | indication | 1010634002 | |
| Intra-Abdominal E. Coli Abscess | indication | ||
| E. Coli Peritonitis | indication | ||
| Skin and Skin Structure Acinetobacter Infection | indication | ||
| E. Coli Gynecological Infections | indication | ||
| Klebsiella Pneumoniae Peritonitis | indication | ||
| Skin and Skin Structure Bacteroides Fragilis Infection | indication | ||
| Bacteroides Gynecological Infections | indication | ||
| Inflammatory Disease of Female Pelvic Organs | indication | ||
| Bacteroides Peritonitis | indication | ||
| Skin and Skin Structure Proteus Infection | indication | ||
| Streptococcal meningitis | off-label use | 4510004 | DOID:11574 |
| Pyrexia of unknown origin | off-label use | 7520000 | |
| Bacterial pneumonia | off-label use | 53084003 | DOID:874 |
| Infection of bone | off-label use | 111253001 | |
| Meningococcal meningitis | off-label use | 192644005 | |
| Sepsis of the newborn | off-label use | 206376005 | |
| Human bite - wound | off-label use | 262555007 | |
| Diverticulitis of gastrointestinal tract | off-label use | 271366000 | |
| Neonatal meningitis | off-label use | 276674008 | |
| Dog bite - wound | off-label use | 283734005 | |
| Cat bite - wound | off-label use | 283782004 | |
| Infective otitis media | off-label use | 312218008 | |
| Diabetic Foot Infection | off-label use | ||
| Kidney disease | contraindication | 90708001 | DOID:557 |
| Infectious mononucleosis | contraindication | 271558008 | DOID:8568 |
| Pseudomembranous enterocolitis | contraindication | 397683000 |
None
None
| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 3.1 | acidic |
| Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
|---|---|---|---|---|---|---|---|---|---|---|
| EQ 500MG BASE/VIAL; EQ 500MG BASE/VIAL;EQ 1GM BASE/VIAL | XACDURO (COPACKAGED) | ENTASIS THERAP | N216974 | May 23, 2023 | RX | POWDER | INTRAVENOUS | 9623014 | April 2, 2033 | TREATMENT OF HOSPITAL-ACQUIRED BACTERIAL PNEUMONIA AND VENTILATOR-ASSOCIATED BACTERIAL PNEUMONIA (HABP/VABP) |
| EQ 500MG BASE/VIAL; EQ 500MG BASE/VIAL;EQ 1GM BASE/VIAL | XACDURO (COPACKAGED) | ENTASIS THERAP | N216974 | May 23, 2023 | RX | POWDER | INTRAVENOUS | 10376499 | Nov. 17, 2035 | TREATMENT OF HOSPITAL-ACQUIRED BACTERIAL PNEUMONIA AND VENTILATOR-ASSOCIATED BACTERIAL PNEUMONIA (HABP/VABP) |
| EQ 500MG BASE/VIAL; EQ 500MG BASE/VIAL;EQ 1GM BASE/VIAL | XACDURO (COPACKAGED) | ENTASIS THERAP | N216974 | May 23, 2023 | RX | POWDER | INTRAVENOUS | 9968593 | Nov. 17, 2035 | TREATMENT OF HOSPITAL-ACQUIRED BACTERIAL PNEUMONIA AND VENTILATOR-ASSOCIATED BACTERIAL PNEUMONIA (HABP/VABP) |
| Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
|---|---|---|---|---|---|---|---|---|---|
| EQ 500MG BASE/VIAL; EQ 500MG BASE/VIAL;EQ 1GM BASE/VIAL | XACDURO (COPACKAGED) | ENTASIS THERAP | N216974 | May 23, 2023 | RX | POWDER | INTRAVENOUS | May 23, 2028 | NEW CHEMICAL ENTITY |
| EQ 500MG BASE/VIAL; EQ 500MG BASE/VIAL;EQ 1GM BASE/VIAL | XACDURO (COPACKAGED) | ENTASIS THERAP | N216974 | May 23, 2023 | RX | POWDER | INTRAVENOUS | May 23, 2033 | GENERATING ANTIBIOTIC INCENTIVES NOW |
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Serine beta-lactamase-like protein LACTB, mitochondrial | Enzyme | IC50 | 5.01 | WOMBAT-PK | |||||
| Beta-lactamase TEM | Enzyme | INHIBITOR | Ki | 6.10 | CHEMBL | CHEMBL | |||
| Beta-lactamase | Enzyme | IC50 | 4.18 | CHEMBL | |||||
| Beta-lactamase SHV-1 | Enzyme | IC50 | 5.41 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 6 | CHEMBL | |||||
| Beta-lactamase OXA-1 | Enzyme | IC50 | 4.66 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 4.57 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.21 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 7.12 | CHEMBL | |||||
| Carbapenem-hydrolizing beta-lactamase SFC-1 | Enzyme | IC50 | 4.64 | CHEMBL | |||||
| Beta-lactamase GES-13 | Enzyme | IC50 | 6.43 | CHEMBL | |||||
| Class D beta-lactamase | Unclassified | IC50 | 4.92 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.62 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.95 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.11 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.40 | CHEMBL | |||||
| Beta-lactamase TEM | Enzyme | Ki | 6.10 | WOMBAT-PK | |||||
| ADC-18 protein | Enzyme | IC50 | 4.93 | CHEMBL | |||||
| Beta-lactamase 1 | Enzyme | IC50 | 4.60 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.52 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.19 | CHEMBL | |||||
| Beta-lactamase | Enzyme | IC50 | 5.52 | CHEMBL |
| ID | Source |
|---|---|
| 4019937 | VUID |
| N0000148022 | NUI |
| D02223 | KEGG_DRUG |
| 69388-84-7 | SECONDARY_CAS_RN |
| 4019381 | VANDF |
| 4019937 | VANDF |
| C0038665 | UMLSCUI |
| CHEBI:9321 | CHEBI |
| 0RN | PDB_CHEM_ID |
| CHEMBL403 | ChEMBL_ID |
| DB09324 | DRUGBANK_ID |
| CHEMBL1200944 | ChEMBL_ID |
| D013407 | MESH_DESCRIPTOR_UI |
| 130313 | PUBCHEM_CID |
| 10769 | IUPHAR_LIGAND_ID |
| 4845 | INN_ID |
| S4TF6I2330 | UNII |
| 10167 | RXNORM |
| 5520 | MMSL |
| d04403 | MMSL |
| 002811 | NDDF |
| 002812 | NDDF |
| 398916003 | SNOMEDCT_US |
| 412516007 | SNOMEDCT_US |
| 96008003 | SNOMEDCT_US |
| Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
|---|---|---|---|---|---|---|---|---|
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0013 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAMUSCULAR | NDA | 26 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0013 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAMUSCULAR | NDA | 26 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0014 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAMUSCULAR | NDA | 26 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0014 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAMUSCULAR | NDA | 26 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0024 | INJECTION, POWDER, FOR SOLUTION | 50 mg | INTRAMUSCULAR | NDA | 25 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0024 | INJECTION, POWDER, FOR SOLUTION | 50 mg | INTRAMUSCULAR | NDA | 25 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0031 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAMUSCULAR | ANDA | 26 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0031 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAMUSCULAR | ANDA | 26 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0032 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAMUSCULAR | ANDA | 26 sections |
| UNASYN | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0049-0032 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAMUSCULAR | ANDA | 26 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0409-2689 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0409-2689 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0409-2987 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0409-2987 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6116 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAVENOUS | ANDA | 24 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6117 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 24 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6118 | INJECTION, POWDER, FOR SOLUTION | 50 mg | INTRAVENOUS | ANDA | 24 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6119 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6120 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6121 | INJECTION, POWDER, FOR SOLUTION | 50 mg | INTRAVENOUS | ANDA | 24 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6122 | INJECTION, POWDER, FOR SOLUTION | 125 mg | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 0641-6123 | INJECTION, POWDER, FOR SOLUTION | 125 mg | INTRAVENOUS | ANDA | 25 sections |
| ampicillin and sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 25021-142 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAVENOUS | ANDA | 25 sections |
| ampicillin and sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 25021-143 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 25 sections |
| ampicillin and sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 25021-144 | INJECTION, POWDER, FOR SOLUTION | 50 mg | INTRAVENOUS | ANDA | 25 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 36000-094 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAVENOUS | ANDA | 26 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 36000-095 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 26 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 44567-150 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 23 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 44567-150 | INJECTION, POWDER, FOR SOLUTION | 1 g | INTRAVENOUS | ANDA | 23 sections |
| Ampicillin and Sulbactam | HUMAN PRESCRIPTION DRUG LABEL | 2 | 44567-210 | INJECTION, POWDER, FOR SOLUTION | 0.50 g | INTRAVENOUS | ANDA | 23 sections |