Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H15N3O4 |
| Molecular Weight | 253.2545 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)OCC1=CC=CC(COC(=O)NC)=N1
InChI
InChIKey=YEKQSSHBERGOJK-UHFFFAOYSA-N
InChI=1S/C11H15N3O4/c1-12-10(15)17-6-8-4-3-5-9(14-8)7-18-11(16)13-2/h3-5H,6-7H2,1-2H3,(H,12,15)(H,13,16)
| Molecular Formula | C11H15N3O4 |
| Molecular Weight | 253.2545 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://www.medoteka.ru/components/pyricarbateCurator's Comment: description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/213636
Sources: http://www.medoteka.ru/components/pyricarbate
Curator's Comment: description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/213636
Parmidin (pyridinol carbamate) is a Soviet drug, has anti-arteriosclerotic (increased vascular resistance) activity, reduces the permeability of blood vessels, it helps to restore disturbed microcirculation in pathological processes. This is mainly due to the influence on kinin system, especially with a decrease in the activity of bradykinin receptors. It also reduces the aggregation of platelets. It’s used to treat: the brain vascular atherosclerosis, heart, limbs; diabetic retinopathy (non-inflammatory lesion of the retina associated with increased levels of sugar in the blood); thrombosis (violation of patency) retinal vein; occlusive disease (inflammation of the inner lining of arteries with a decrease in their lumen); trophic leg ulcers (slow-healing skin defects caused by malnutrition). Ointment is used in neurodermatitis (skin disease caused by disturbance of the central nervous system), Lichen sclerosus (teardrop scleroderma) genital organs of children, as well as a prophylactic and therapeutic agent against radiation skin lesions.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL4308 Sources: DOI: 10.1007/BF00776332 Tugusheva, N.Z., Ershov, L.V., Granik, V.G. et al. Pharm Chem J (1986) 20: 483. doi:10.1007/BF00776332 |
|||
Target ID: CHEMBL3157 Sources: DOI: 10.1007/BF00776332 Tugusheva, N.Z., Ershov, L.V., Granik, V.G. et al. Pharm Chem J (1986) 20: 483. doi:10.1007/BF00776332 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Parmidin tablets 0,25 g Approved UseAtherosclerosis of vessels of the brain, heart, limbs, eyes (comprehensive treatment and prevention). |
|||
| Palliative | Parmidin Approved UseUnknown |
|||
| Palliative | Parmidin Approved UseUnknown |
|||
| Palliative | Parmidin Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
18.28 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6745304/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
21.8 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6745304/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE serum | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
14.5 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/501551/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
|
15.8 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/501551/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
187.36 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6745304/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
249.6 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6745304/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE serum | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
132.77 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/501551/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
|
142.28 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/501551/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
5.86 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6745304/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
6.56 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/6745304/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE serum | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
4.8 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/501551/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
|
4.8 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/501551/ |
1 g single, oral dose: 1 g route of administration: Oral experiment type: SINGLE co-administered: |
PYRICARBATE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
Doses
| Dose | Population | Adverse events |
|---|---|---|
2250 mg 1 times / day multiple, oral Highest studied dose Dose: 2250 mg, 1 times / day Route: oral Route: multiple Dose: 2250 mg, 1 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
Other AEs: Headache, Chest ache... |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Chest ache | 1 pt | 2250 mg 1 times / day multiple, oral Highest studied dose Dose: 2250 mg, 1 times / day Route: oral Route: multiple Dose: 2250 mg, 1 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
| Headache | mild, 1 pt | 2250 mg 1 times / day multiple, oral Highest studied dose Dose: 2250 mg, 1 times / day Route: oral Route: multiple Dose: 2250 mg, 1 times / day Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.rlsnet.ru/tn_index_id_11562.htm
Curator's Comment: http://www.piluli.kharkov.ua/drugs/drug/531/
Oral: 0.25-0.75 g 3-4 times/day. The course: 2-6 months.
Topical:- 2-3 times a day for 10-12 days
Route of Administration:
Other
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/772874
Unknown
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:47:52 GMT 2025
by
admin
on
Mon Mar 31 18:47:52 GMT 2025
|
| Record UNII |
81R511UV73
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Brand Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29703
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
SUB10164MIG
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
5011
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
C152114
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
100000080866
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
217-538-9
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
4990
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
CHEMBL1620144
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
D011727
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
m9358
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | Merck Index | ||
|
DTXSID5045708
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
2329
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
81R511UV73
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
1882-26-4
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | |||
|
8997
Created by
admin on Mon Mar 31 18:47:52 GMT 2025 , Edited by admin on Mon Mar 31 18:47:52 GMT 2025
|
PRIMARY | RxNorm |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |