Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H13ClFN3 |
| Molecular Weight | 325.767 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NC=C2CN=C(C3=CC=CC=C3F)C4=CC(Cl)=CC=C4N12
InChI
InChIKey=DDLIGBOFAVUZHB-UHFFFAOYSA-N
InChI=1S/C18H13ClFN3/c1-11-21-9-13-10-22-18(14-4-2-3-5-16(14)20)15-8-12(19)6-7-17(15)23(11)13/h2-9H,10H2,1H3
| Molecular Formula | C18H13ClFN3 |
| Molecular Weight | 325.767 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Midazolam, previously marketed under the trade name Versed, is a medication used for anesthesia, procedural sedation, trouble sleeping, and severe agitation. Midazolam is a short-acting benzodiazepine central nervous system (CNS) depressant. Pharmacodynamic properties of midazolam and its metabolites, which are similar to those of other benzodiazepines, include sedative, anxiolytic, amnesic and hypnotic activities. Benzodiazepine pharmacologic effects appear to result from reversible interactions with the γ-amino butyric acid (GABA) benzodiazepine receptor in the CNS, the major inhibitory neurotransmitter in the central nervous system. The action of midazolam is readily reversed by the benzodiazepine receptor antagonist, flumazenil.
Data from published reports of studies in pediatric patients clearly demonstrate that oral midazolam provides safe and effective sedation and anxiolysis prior to surgical procedures that require anesthesia as well as before other procedures that require sedation but may not require anesthesia. The most commonly reported effective doses range from 0.25 to 1 mg/kg in children (6 months to <16 years). The single most commonly reported effective dose is 0.5 mg/kg. Time to onset of effect is most frequently reported as 10 to 20 minutes.
The effects of midazolam on the CNS are dependent on the dose administered, the route of administration, and the presence or absence of other medications.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
| 2.0 nM [Ki] | |||
Target ID: CHEMBL1810 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2566295 |
3.2 µM [Ki] | ||
Target ID: CHEMBL232 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10565838 |
183.0 µM [Ki] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Midazolam Approved UseMidazolam hydrochloride syrup is indicated for use in pediatric patients for sedation, anxiolysis and amnesia prior to diagnostic, therapeutic or endoscopic procedures or before induction of anesthesia.
Midazolam hydrochloride syrup is intended for use in monitored settings only and not for chronic or home use (see WARNINGS). MIDAZOLAM HYDROCHLORIDE SYRUP MUST BE USED AS SPECIFIED IN THE LABEL.
Midazolam is associated with a high incidence of partial or complete impairment of recall for the next several hours Launch Date1985 |
|||
| Primary | Midazolam Approved UseMidazolam HCl syrup is indicated for use in pediatric patients for sedation, anxiolysis and amnesia prior to diagnostic, therapeutic or endoscopic procedures or before induction of anesthesia. Midazolam HCl syrup is intended for use in monitored settings only and not for chronic or home use (see WARNINGS). MIDAZOLAM HCl SYRUP MUST BE USED AS SPECIFIED IN THE LABEL. Midazolam is associated with a high incidence of partial or complete impairment of recall for the next several hours Launch Date1985 |
|||
| Primary | Midafresa Approved UseEpilepsy Launch Date2014 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
35.124 ng/mL Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01989169 |
6 mg single, oral dose: 6 mg route of administration: oral experiment type: single co-administered: |
MIDAZOLAM plasma | Homo sapiens population: healthy age: Adults sex: food status: |
|
113.9 ng/mL |
10 mg single, intramuscular dose: 10 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
MIDAZOLAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
54.7 ng/mL |
5 mg single, nasal dose: 5 mg route of administration: Nasal experiment type: SINGLE co-administered: |
MIDAZOLAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
30 nM*h Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01361217 |
2 mg single, oral dose: 2 mg route of administration: oral experiment type: single co-administered: |
MIDAZOLAM plasma | Homo sapiens population: healthy age: adults sex: food status: |
|
103.348 ng*h/mL Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01989169 |
6 mg single, oral dose: 6 mg route of administration: oral experiment type: single co-administered: |
MIDAZOLAM plasma | Homo sapiens population: healthy age: Adults sex: food status: |
|
100.935 ng*h/mL Clinical Trial https://clinicaltrials.gov/ct2/show/NCT01989169 |
6 mg single, oral dose: 6 mg route of administration: oral experiment type: single co-administered: |
MIDAZOLAM plasma | Homo sapiens population: healthy age: Adults sex: food status: |
|
402.7 ng × h/mL |
10 mg single, intramuscular dose: 10 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
MIDAZOLAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
126.2 ng × h/mL |
5 mg single, nasal dose: 5 mg route of administration: Nasal experiment type: SINGLE co-administered: |
MIDAZOLAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
3% |
10 mg single, intramuscular dose: 10 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
MIDAZOLAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
3% |
5 mg single, nasal dose: 5 mg route of administration: Nasal experiment type: SINGLE co-administered: |
MIDAZOLAM plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
5 mg single, intranasal MTD Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unknown, 18 - 65 years Health Status: unknown Age Group: 18 - 65 years Sex: unknown Sources: |
Other AEs: Nausea, Hypotension... |
5 mg 1 times / month multiple, intranasal Recommended Dose: 5 mg, 1 times / month Route: intranasal Route: multiple Dose: 5 mg, 1 times / month Sources: |
unhealthy, > 12 years Health Status: unhealthy Age Group: > 12 years Sex: unknown Sources: |
Disc. AE: Nasal discomfort, Somnolence... Other AEs: Nasal discomfort, Somnolence... AEs leading to discontinuation/dose reduction: Nasal discomfort (1 patient) Other AEs:Somnolence (1 patient) Nasal discomfort (12.4%) Sources: Somnolence (9.3%) |
5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unknown, adult and children Health Status: unknown Age Group: adult and children Sex: M+F Sources: |
Other AEs: Hypoxemia, Hypotension... Other AEs: Hypoxemia (90 patients) Sources: Hypotension (5 patients) |
5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
Other AEs: Somnolence, Headache... Other AEs: Somnolence (10%) Sources: Headache (7%) Dysarthria (2%) Nasal discomfort (5%) Throat irritation (2%) Rhinorrhea (3%) Lacrimation increased (1%) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Hypotension | 5 mg single, intranasal MTD Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unknown, 18 - 65 years Health Status: unknown Age Group: 18 - 65 years Sex: unknown Sources: |
|
| Nausea | 5 mg single, intranasal MTD Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unknown, 18 - 65 years Health Status: unknown Age Group: 18 - 65 years Sex: unknown Sources: |
|
| Nasal discomfort | 1 patient Disc. AE |
5 mg 1 times / month multiple, intranasal Recommended Dose: 5 mg, 1 times / month Route: intranasal Route: multiple Dose: 5 mg, 1 times / month Sources: |
unhealthy, > 12 years Health Status: unhealthy Age Group: > 12 years Sex: unknown Sources: |
| Somnolence | 1 patient Disc. AE |
5 mg 1 times / month multiple, intranasal Recommended Dose: 5 mg, 1 times / month Route: intranasal Route: multiple Dose: 5 mg, 1 times / month Sources: |
unhealthy, > 12 years Health Status: unhealthy Age Group: > 12 years Sex: unknown Sources: |
| Nasal discomfort | 12.4% | 5 mg 1 times / month multiple, intranasal Recommended Dose: 5 mg, 1 times / month Route: intranasal Route: multiple Dose: 5 mg, 1 times / month Sources: |
unhealthy, > 12 years Health Status: unhealthy Age Group: > 12 years Sex: unknown Sources: |
| Somnolence | 9.3% | 5 mg 1 times / month multiple, intranasal Recommended Dose: 5 mg, 1 times / month Route: intranasal Route: multiple Dose: 5 mg, 1 times / month Sources: |
unhealthy, > 12 years Health Status: unhealthy Age Group: > 12 years Sex: unknown Sources: |
| Hypotension | 5 patients | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unknown, adult and children Health Status: unknown Age Group: adult and children Sex: M+F Sources: |
| Hypoxemia | 90 patients | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unknown, adult and children Health Status: unknown Age Group: adult and children Sex: M+F Sources: |
| Lacrimation increased | 1% | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Somnolence | 10% | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Dysarthria | 2% | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Throat irritation | 2% | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Rhinorrhea | 3% | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Nasal discomfort | 5% | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
| Headache | 7% | 5 mg single, intranasal Recommended Dose: 5 mg Route: intranasal Route: single Dose: 5 mg Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sex: unknown Sources: |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| yes [Ki 3.7 uM] | ||||
Sources: https://pubmed.ncbi.nlm.nih.gov/15544435/ Page: 9.0 |
yes [Ki 5.8 uM] |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/211321Orig1s000ClinPharmR.pdf#page=11 Page: 11,12 |
major | yes (co-administration study) Comment: INHIBITORS: Coadministration with cimetidine: AUC increase of MDZ=10-102%; diltiazem: AUC increase of MDZ=275%; erythromycin: AUC increase of MDZ=281-341; fluconazole: AUC increase of MDZ=250%; grapefruit juice: AUC increase of 52%; itraconazole: AUC increase of MDZ=240-980%; ketoconazole: AUC increase of MDZ=1490%; ranitidine: AUC increase of MDZ=9-66%. INDUCERS: coadministration with carbamazepine: AUC decrease of MDZ=94%; phenytoin: AUC decrease of MDZ=94%; rifampin: AUC decrease of MDZ=96%; Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/211321Orig1s000ClinPharmR.pdf#page=11 Page: 11,12 |
||
| minor | ||||
| minor | ||||
| minor | ||||
| no | ||||
| no | ||||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/18256203/ Page: 8.0 |
yes |
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
PubMed
| Title | Date | PubMed |
|---|---|---|
| Onset and duration of action of rocuronium--from tracheal intubation, through intense block to complete recovery. | 2001-05 |
|
| Characterization of discriminative stimulus effects of the neuroactive steroid pregnanolone. | 2001-05 |
|
| Inhibition of CYP3A4 in a rapid microtiter plate assay using recombinant enzyme and in human liver microsomes using conventional substrates. | 2001-05 |
|
| Management of background pain and anxiety in critically burned children requiring protracted mechanical ventilation. | 2001-04-17 |
|
| Burn patients' pain and anxiety experiences. | 2001-04-17 |
|
| Propofol vs midazolam for ICU sedation : a Canadian multicenter randomized trial. | 2001-04 |
|
| A lack of evidence of superiority of propofol versus midazolam for sedation in mechanically ventilated critically ill patients: a qualitative and quantitative systematic review. | 2001-04 |
|
| The preemptive analgesic effect of intraarticular bupivacaine and morphine after ambulatory arthroscopic knee surgery. | 2001-04 |
|
| Stress response in infants undergoing cardiac surgery: a randomized study of fentanyl bolus, fentanyl infusion, and fentanyl-midazolam infusion. | 2001-04 |
|
| Using intranasal midazolam spray to prevent claustrophobia induced by MR imaging. | 2001-04 |
|
| Distinct functional and pharmacological properties of tonic and quantal inhibitory postsynaptic currents mediated by gamma-aminobutyric acid(A) receptors in hippocampal neurons. | 2001-04 |
|
| Metabolism of levo-alpha-Acetylmethadol (LAAM) by human liver cytochrome P450: involvement of CYP3A4 characterized by atypical kinetics with two binding sites. | 2001-04 |
|
| Prediction of midazolam-CYP3A inhibitors interaction in the human liver from in vivo/in vitro absorption, distribution, and metabolism data. | 2001-04 |
|
| A retrospective study on the effectiveness of intranasal midazolam in pediatric burn patients. | 2001-03-03 |
|
| Synergistic analgesic effects of intrathecal midazolam and NMDA or AMPA receptor antagonists in rats. | 2001-03 |
|
| Selective spinal anesthesia for outpatient laparoscopy. II: epinephrine and spinal cord function. | 2001-03 |
|
| Drugs and syringe drivers: a survey of adult specialist palliative care practice in the United Kingdom and Eire. | 2001-03 |
|
| Midazolam reduces the dose of propofol required for induction of anaesthesia and laryngeal mask airway insertion. | 2001-03 |
|
| Re: Koshy et al.--The use of propofol versus midazolam. | 2001-03 |
|
| Lack of correlation between in vitro inhibition of CYP3A-mediated metabolism by a PPAR-gamma agonist and its effect on the clinical pharmacokinetics of midazolam, an in vivo probe of CYP3A activity. | 2001-03 |
|
| Comparison of midazolam with or without fentanyl for conscious sedation and hemodynamics in coronary angiography. | 2001-03 |
|
| Anaesthetic technique for transoesophageal echocardiography in children. | 2001-03 |
|
| The comparison of midazolam and topical lidocaine spray versus the combination of midazolam, meperidine, and topical lidocaine spray to sedate patients for upper endoscopy. | 2001-03 |
|
| Propofol is not effective for hyperventilation syndrome. | 2001-03 |
|
| The effect of anxiety and personality on the pharmacokinetics of oral midazolam. | 2001-03 |
|
| [Premedication in ambulatory surgery]. | 2001-02-12 |
|
| [Premedication for endoscopy]. | 2001-02-02 |
|
| Triazolam discrimination in squirrel monkeys distinguishes high-efficacy agonists from other benzodiazepines and non-benzodiazepine drugs. | 2001-02 |
|
| Sedation for cataract surgery. | 2001-02 |
|
| Preparation, premedication, and surveillance. | 2001-02 |
|
| [Epileptogenic drugs in anesthesia]. | 2001-02 |
|
| Propofol as a continuous infusion during cardiopulmonary bypass does not affect changes in serum free fatty acids. | 2001-02 |
|
| Small doses of remifentanil or sufentanil for blunting cardiovascular changes induced by tracheal intubation: a double-blind comparison. | 2001-02 |
|
| Bilateral frontal haemorrhages associated with continuous spinal analgesia. | 2001-02 |
|
| The use of thiopentone/propofol admixture for laryngeal mask airway insertion. | 2001-02 |
|
| Transdermal delivery of antisense oligonucleotides can induce changes in gene expression in vivo. | 2001-02 |
|
| [Fastrach laryngeal mask, sevoflurane and remifentanil: an anesthetic alternative for the myasthenic patient]. | 2001-02 |
|
| Pharmacoeconomic assessment of propofol 2% used for prolonged sedation. | 2001-02 |
|
| [Anesthetic management for the correction of pectus excavatum using pectus bar under video-assistance]. | 2001-02 |
|
| [Anesthetic management for left ventricular assist device implantation in patients waiting for heart transplantation]. | 2001-02 |
|
| Inhibitory effects of CYP3A4 substrates and their metabolites on P-glycoprotein-mediated transport. | 2001-02 |
|
| A randomized prospective comparative study of general versus epidural anesthesia for transcervical hysteroscopic endometrial resection. | 2001-02 |
|
| Oral transmucosal midazolam premedication for preschool children. | 2001-02 |
|
| Sedation for children requiring wound repair: a randomised controlled double blind comparison of oral midazolam and oral ketamine. | 2001-01 |
|
| Intra-nasal midazolam in conscious sedation of young paediatric dental patients. | 2001-01 |
|
| Ketamine-midazolam total intravenous anaesthesia for prolonged abdominal surgery. | 2001-01 |
|
| Pulse oximetry saturation levels during routine unsedated diagnostic upper gastrointestinal endoscopy. | 2001-01 |
|
| [Anesthetic experience of emergency coronary artery bypass graft operation in a patient with cardioamyloidosis]. | 2001-01 |
|
| [Anesthetic management for mitral valve replacement in a patient with idiopathic hypereosinophilic syndrome]. | 2001-01 |
|
| Computerised advice on drug dosage to improve prescribing practice. | 2001 |
Patents
Sample Use Guides
Midazolam hydrochloride syrup is indicated for use as a single dose (0.25 to 1 mg/kg with a maximum dose of 20 mg) for preprocedural sedation and anxiolysis in pediatric patients. Midazolam hydrochloride syrup is not intended for chronic administration.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8173965
Midazolam (1 uM) decreased GABA-activated currents in acutely dissociated neurons, isolated from the medial septum/nucleus of the diagonal band (MS/nDB) of the adult rat brains.
| Substance Class |
Chemical
Created
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| Record UNII |
R60L0SM5BC
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Validated (UNII)
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DEA NO. |
2884
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WHO-VATC |
QN05CD08
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FDA ORPHAN DRUG |
514115
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LIVERTOX |
NBK548691
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FDA ORPHAN DRUG |
373912
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WHO-ESSENTIAL MEDICINES LIST |
1.3
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FDA ORPHAN DRUG |
622817
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FDA ORPHAN DRUG |
507615
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NCI_THESAURUS |
C1012
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FDA ORPHAN DRUG |
217405
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WHO-ATC |
N05CD08
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NDF-RT |
N0000175694
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FDA ORPHAN DRUG |
508215
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WHO-ESSENTIAL MEDICINES LIST |
8.4
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FDA ORPHAN DRUG |
277809
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DTXSID5023320
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1443599
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4497
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MIDAZOLAM
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Midazolam
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m7531
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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3342
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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6931
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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4192
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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CHEMBL655
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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7581
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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6751
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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100000080626
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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R60L0SM5BC
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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1802
Created by
admin on Mon Mar 31 18:09:06 GMT 2025 , Edited by admin on Mon Mar 31 18:09:06 GMT 2025
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| Related Record | Type | Details | ||
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METABOLIC ENZYME -> SUBSTRATE | |||
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METABOLIC ENZYME -> SUBSTRATE | |||
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BINDER->LIGAND |
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METABOLIC ENZYME -> INHIBITOR | |||
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METABOLIC ENZYME -> SUBSTRATE |
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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METABOLIC ENZYME -> SUBSTRATE | |||
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METABOLIC ENZYME -> INHIBITOR | |||
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METABOLIC ENZYME -> SUBSTRATE | |||
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TRANSPORTER -> INHIBITOR | |||
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METABOLIC ENZYME -> SUBSTRATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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METABOLITE -> PARENT |
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METABOLITE ACTIVE -> PARENT |
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METABOLITE -> PARENT |
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METABOLITE -> PARENT | |||
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METABOLITE ACTIVE -> PARENT |
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METABOLITE -> PARENT |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| Volume of Distribution | PHARMACOKINETIC |
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| Biological Half-life | PHARMACOKINETIC |
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