Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C9H15N5O3.2ClH |
Molecular Weight | 314.169 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.[H][C@@]1(CNC2=C(N1)C(=O)N=C(N)N2)[C@@H](O)[C@H](C)O
InChI
InChIKey=RKSUYBCOVNCALL-NTVURLEBSA-N
InChI=1S/C9H15N5O3.2ClH/c1-3(15)6(16)4-2-11-7-5(12-4)8(17)14-9(10)13-7;;/h3-4,6,12,15-16H,2H2,1H3,(H4,10,11,13,14,17);2*1H/t3-,4+,6-;;/m0../s1
Molecular Formula | C9H15N5O3 |
Molecular Weight | 241.2471 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionCurator's Comment: description was created based on several sources, including
http://www.biomarin.com/products/kuvan
Curator's Comment: description was created based on several sources, including
http://www.biomarin.com/products/kuvan
Sapropterin dihydrochloride, the active pharmaceutical ingredient in Kuvan Tablets, is a synthetic preparation of the dihydrochloride salt of naturally occurring tetrahydrobiopterin (BH4). Kuvan is indicated to reduce blood phenylalanine (Phe) levels in patients with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4-) responsive Phenylketonuria (PKU). Kuvan is to be used in conjunction with a Phe-restricted diet. Kuvan has received orphan drug designation from both the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMEA). Kuvan is a synthetic form of BH4, the cofactor for the enzyme phenylalanine hydroxylase (PAH). PAH hydroxylates Phe through an oxidative reaction to form tyrosine. In patients with PKU, PAH activity is absent or deficient. Treatment with BH4 can activate residual PAH enzyme, improve the normal oxidative metabolism of Phe, and decrease Phe levels in some patients.
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3076 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10872454 |
|||
Target ID: CHEMBL4803 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12003347 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | KUVAN Approved UseKuvan® (sapropterin dihydrochloride) is indicated to reduce blood phenylalanine (Phe) levels in patients with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4-) responsive Phenylketonuria (PKU). Kuvan is to be used in conjunction with a Phe-restricted diet. Kuvan is a phenylalanine hydroxylase activator indicated to reduce blood phenylalanine (Phe) levels in patients with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin‑ (BH4‑) responsive Phenylketonuria (PKU). Kuvan is to be used in conjunction with a Phe‑restricted diet (1). Launch Date2007 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
84.1 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20206791/ |
10 mg/kg single, oral dose: 10 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
SAPROPTERIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
559 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20206791/ |
10 mg/kg single, oral dose: 10 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
SAPROPTERIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
3.67 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/20206791/ |
10 mg/kg single, oral dose: 10 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
SAPROPTERIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Doses
Dose | Population | Adverse events |
---|---|---|
20 mg/kg 1 times / day multiple, oral Recommended Dose: 20 mg/kg, 1 times / day Route: oral Route: multiple Dose: 20 mg/kg, 1 times / day Sources: Page: p.705 |
unhealthy, 7.7 n = 33 Health Status: unhealthy Condition: Phenylketonuria Age Group: 7.7 Sex: M+F Population Size: 33 Sources: Page: p.705 |
|
45 mg/kg single, oral Overdose Dose: 45 mg/kg Route: oral Route: single Dose: 45 mg/kg Sources: Page: p.10 |
unhealthy, child n = 1 Health Status: unhealthy Condition: Hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4 -) responsive Phenylketonuria Age Group: child Population Size: 1 Sources: Page: p.10 |
Disc. AE: Hyperactivity... AEs leading to discontinuation/dose reduction: Hyperactivity Sources: Page: p.10 |
20 mg/kg 1 times / day multiple, oral Recommended Dose: 20 mg/kg, 1 times / day Route: oral Route: multiple Dose: 20 mg/kg, 1 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4 -) responsive Phenylketonuria Sources: Page: p.1 |
Disc. AE: Hypersensitivity reaction, Anaphylaxis... AEs leading to discontinuation/dose reduction: Hypersensitivity reaction Sources: Page: p.1Anaphylaxis Gastritis Hyperactivity |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Hyperactivity | Disc. AE | 45 mg/kg single, oral Overdose Dose: 45 mg/kg Route: oral Route: single Dose: 45 mg/kg Sources: Page: p.10 |
unhealthy, child n = 1 Health Status: unhealthy Condition: Hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4 -) responsive Phenylketonuria Age Group: child Population Size: 1 Sources: Page: p.10 |
Anaphylaxis | Disc. AE | 20 mg/kg 1 times / day multiple, oral Recommended Dose: 20 mg/kg, 1 times / day Route: oral Route: multiple Dose: 20 mg/kg, 1 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4 -) responsive Phenylketonuria Sources: Page: p.1 |
Gastritis | Disc. AE | 20 mg/kg 1 times / day multiple, oral Recommended Dose: 20 mg/kg, 1 times / day Route: oral Route: multiple Dose: 20 mg/kg, 1 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4 -) responsive Phenylketonuria Sources: Page: p.1 |
Hyperactivity | Disc. AE | 20 mg/kg 1 times / day multiple, oral Recommended Dose: 20 mg/kg, 1 times / day Route: oral Route: multiple Dose: 20 mg/kg, 1 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4 -) responsive Phenylketonuria Sources: Page: p.1 |
Hypersensitivity reaction | Disc. AE | 20 mg/kg 1 times / day multiple, oral Recommended Dose: 20 mg/kg, 1 times / day Route: oral Route: multiple Dose: 20 mg/kg, 1 times / day Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4 -) responsive Phenylketonuria Sources: Page: p.1 |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
---|---|---|
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 15.0 |
inconclusive | |||
Page: 15.0 |
inconclusive | |||
Page: 13.0 |
no | |||
Page: 13.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
no | |||
Page: 15.0 |
yes |
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 4.0 |
no |
Tox targets
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 39, 40 |
Sample Use Guides
The recommended starting dose is 10 mg/kg/day taken once daily. Response to therapy is determined by change in blood Phe following treatment with drug at 10 mg/kg/day for a period of up to 1 month. Blood Phe levels should be checked after 1 week of treatment and periodically for up to a month. If blood Phe does not decrease from baseline at 10 mg/kg/day, the dose may be increased to 20 mg/kg/day. Patients whose blood Phe does not decrease after 1 month of treatment at 20 mg/kg/day are non-responders, and treatment should be discontinued in these patients. Once responsiveness to drug has been established, the dosage may be adjusted within the range of 5 to 20 mg/kg/day according to response to therapy. Doses above 20 mg/kg/day have not been evaluated in clinical trials.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9237256
The effect of tetrahydrobiopterin (BH4, SAPROPTERIN) on subunit structure and activity of microsomal and cytosolic Type III nitric oxide synthase (NOS III) was compared. BH4 activates NOS III in the primordial human placenta by promoting its subunit assembly in the membrane, while cytosolic NOS III is relatively insensitive to BH4. Incubation of microsomal membranes with 50 microM final concentration BH4 for 10 min at 37 degrees C resulted in a striking conversion of monomeric NOS III into a protein having the characteristics (electrophoretic mobility, resistance to sodium dodecyl sulphate) of the homodimeric form. In contrast, BH4 induced significantly less marked changes in the NOS III dimer content of cytosolic fractions. Enzyme activity in microsomes is stimulated approximately 6-fold upon addition of 50 microM BH4, while only a 2-fold activation is detectable in cytosolic fractions.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:04:22 GMT 2023
by
admin
on
Fri Dec 15 16:04:22 GMT 2023
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Record UNII |
RG277LF5B3
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C275
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EMA ASSESSMENT REPORTS |
KUVAN (AUTHORIZED: PHENYLKETONURIAS)
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m9775
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100000091700
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ACTIVE MOIETY |