Stem definition | Drug id | CAS RN |
---|---|---|
5462 | 1207753-03-4 |
None
Property | Value | Reference |
---|---|---|
BDDCS (Biopharmaceutical Drug Disposition Classification System) | 2 | Bocci G, Oprea TI, Benet LZ |
Date | Agency | Company | Orphan |
---|---|---|---|
June 1, 2021 | FDA | SCYNEXIS |
None
None
None
None
Source | Code | Description |
---|---|---|
ATC | J02AX07 | ANTIINFECTIVES FOR SYSTEMIC USE ANTIMYCOTICS FOR SYSTEMIC USE ANTIMYCOTICS FOR SYSTEMIC USE Other antimycotics for systemic use |
FDA CS | M0022020 | Triterpenes |
FDA MoA | N0000020027 | Glucan Synthase Inhibitors |
MeSH PA | D000890 | Anti-Infective Agents |
MeSH PA | D000935 | Antifungal Agents |
FDA EPC | N0000193966 | Triterpenoid Antifungal |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Vulvovaginal candidiasis | indication | 72605008 | DOID:2272 |
Candidiasis of vagina | indication | 72934000 | |
Pregnancy, function | contraindication | 289908002 |
None
None
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Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
---|---|---|---|---|---|---|---|---|---|---|
EQ 150MG BASE | BREXAFEMME | SCYNEXIS | N214900 | June 1, 2021 | RX | TABLET | ORAL | 8188085 | Aug. 28, 2030 | TREATMENT OF ADULT AND POST-MENARCHAL PEDIATRIC FEMALES WITH VULVOVAGINAL CANDIDIASIS (VVC) |
EQ 150MG BASE | BREXAFEMME | SCYNEXIS | N214900 | June 1, 2021 | RX | TABLET | ORAL | 10370406 | Jan. 19, 2035 | TREATMENT OF ADULT AND POST-MENARCHAL PEDIATRIC FEMALES WITH VULVOVAGINAL CANDIDIASIS (VVC) |
EQ 150MG BASE | BREXAFEMME | SCYNEXIS | N214900 | June 1, 2021 | RX | TABLET | ORAL | 11534433 | June 10, 2039 | REDUCTION IN THE INCIDENCE OF RECURRENT VULVOVAGINAL CANDIDIASIS (RVVC) IN ADULT AND POST-MENARCHAL PEDIATRIC FEMALES |
EQ 150MG BASE | BREXAFEMME | SCYNEXIS | N214900 | June 1, 2021 | RX | TABLET | ORAL | 11534433 | June 10, 2039 | TREATMENT OF ADULT AND POST-MENARCHAL PEDIATRIC FEMALES WITH VULVOVAGINAL CANDIDIASIS (VVC) |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
---|---|---|---|---|---|---|---|---|---|
EQ 150MG BASE | BREXAFEMME | SCYNEXIS | N214900 | June 1, 2021 | RX | TABLET | ORAL | Nov. 30, 2025 | REDUCTION IN THE INCIDENCE OF RECURRENT VULVOVAGINAL CANDIDIASIS (RVVC) INADULT AND POST-MENARCHAL PEDIATRIC FEMALES |
EQ 150MG BASE | BREXAFEMME | SCYNEXIS | N214900 | June 1, 2021 | RX | TABLET | ORAL | June 1, 2026 | NEW CHEMICAL ENTITY |
EQ 150MG BASE | BREXAFEMME | SCYNEXIS | N214900 | June 1, 2021 | RX | TABLET | ORAL | June 1, 2031 | GENERATING ANTIBIOTIC INCENTIVES NOW |
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
Beta-1,3-glucan synthase catalytic subunit 1 | Enzyme | INHIBITOR | IC50 | 8.35 | SCIENTIFIC LITERATURE | DRUG LABEL | |||
1,3-Beta-D-glucan-UDP glucosyltransferase | Enzyme | INHIBITOR | IC50 | 7.83 | SCIENTIFIC LITERATURE | SCIENTIFIC LITERATURE | |||
1,3-Beta-D-glucan-UDP glucosyltransferase | Enzyme | INHIBITOR | IC50 | 8.97 | SCIENTIFIC LITERATURE | SCIENTIFIC LITERATURE |
ID | Source |
---|---|
D11544 | KEGG_DRUG |
A92JFM5XNU | UNII |
1965291-08-0 | SECONDARY_CAS_RN |
C5206403 | UMLSCUI |
CHEMBL4297513 | ChEMBL_ID |
46871657 | PUBCHEM_CID |
DB12471 | DRUGBANK_ID |
CHEMBL4298168 | ChEMBL_ID |
10597 | INN_ID |
018755 | NDDF |
018756 | NDDF |
4040654 | VANDF |
2560213 | RXNORM |
347181 | MMSL |
39565 | MMSL |
d09756 | MMSL |
C569338 | MESH_SUPPLEMENTAL_RECORD_UI |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
BREXAFEMME | HUMAN PRESCRIPTION DRUG LABEL | 1 | 75788-115 | TABLET, FILM COATED | 150 mg | ORAL | NDA | 34 sections |
BREXAFEMME | HUMAN PRESCRIPTION DRUG LABEL | 1 | 75788-115 | TABLET, FILM COATED | 150 mg | ORAL | NDA | 34 sections |
BREXAFEMME | HUMAN PRESCRIPTION DRUG LABEL | 1 | 75788-115 | TABLET, FILM COATED | 150 mg | ORAL | NDA | 34 sections |