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boceprevir

chemical compound
Class type of: chemical compound Q410551

Facts

16 properties
Instance of
group of stereoisomers
Subclass of
chemical compound
Has use
medication
Active ingredient in
Victrelis
Canonical SMILES
CC1(C2C1C(N(C2)C(=O)C(C(C)(C)C)NC(=O)NC(C)(C)C)C(=O)NC(CC3CCC3)C(=O)C(=O)N)C
Catalog
CAS COVID-19 Anti-Viral Candidate Compounds
Chemical formula
C₂₇H₄₅N₅O₅
Defined daily dose
+2.4
Isomeric SMILES
CC1([C@@H]2[C@H]1[C@H](N(C2)C(=O)[C@H](C(C)(C)C)NC(=O)NC(C)(C)C)C(=O)NC(CC3CCC3)C(=O)C(=O)N)C
LiverTox likelihood score
LiverTox toxicity likelihood category E*
Mass
+519.34207
Medical condition treated
hepatitis C, liver cirrhosis
Physically interacts with
cathepsin A
Pregnancy category
US pregnancy category X
Subject has role
antiviral drug, bactericide
World Health Organisation international non-proprietary name
boceprevir
🏷️ Also known as
en boceprevir en SCH 503034 en SCH-503034 ar بوسبريفير de Victrelis fa بوسپرویر fi Bosepreviiri id Boseprevir ja ボセプレビル pl boceprewir uk боцепревір
🔖 Identifiers · 32
OpenAlex ID
C2777159539
ATC code
J05AE12, J05AP03
CAS Registry Number
394730-60-0
ChEBI ID
68621
ChEMBL ID
CHEMBL218394
ChemSpider ID
8499830
DSSTOX compound identifier
DTXCID601387968
DSSTox substance ID
DTXSID30960103
DrugBank ID
DB08873
DrugCentral ID
4172
EC number
800-043-2
ECHA Substance Infocard ID
100.226.246
Show all 32 identifiers +20
Freebase ID
/m/043p8j0
Guide to Pharmacology Ligand ID
7876
HSDB ID
8081
InChI
InChI=1S/C27H45N5O5/c1-25(2,3)20(30-24(37)31-26(4,5)6)23(36)32-13-15-17(27(15,7)8)18(32)22(35)29-16(19(33)21(28)34)12-14-10-9-11-14/h14-18,20H,9-13H2,1-8H3,(H2,28,34)(H,29,35)(H2,30,31,37)/t15-,16?,17-,18-,20+/m0/s1
InChIKey
LHHCSNFAOIFYRV-DOVBMPENSA-N
KEGG ID
D08876
LiverTox ID
Boceprevir
MeSH descriptor ID
C512204
MedlinePlus drug identifier
a611039
Microsoft Academic ID (discontinued)
2777159539
NDF-RT ID
N0000182738
Probes And Drugs ID
PD008951
PubChem CID
10324367
Reaxys registry number
10502086
RxNorm CUI
1102129
ScienceDirect topic ID
agricultural-and-biological-sciences/boceprevir
SureChEMBL ID
640836
UMLS CUI
C1738934
UNII
89BT58KELH
UniChem compound ID
198935

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Medical condition treated 2
liver cirrhosis, hepatitis C
Subject has role 2
antiviral drug, bactericide
← Drug or therapy used for treatment 2
liver cirrhosis, hepatitis C
Has use 1
medication
Physically interacts with 1
cathepsin A
Subclass of 1
chemical compound
← Physically interacts with 1
cathepsin A
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Summary

boceprevir is a group of stereoisomers[1]. boceprevir is a type of chemical compound[2].

Key Facts

  • Physically interacts with: Cathepsin A[3]
  • Canonical SMILES: CC1(C2C1C(N(C2)C(=O)C(C(C)(C)C)NC(=O)NC(C)(C)C)C(=O)NC(CC3CCC3)C(=O)C(=O)N)C[4]
  • Chemical formula: C₂₇H₄₅N₅O₅[5]
  • Has use: medication[6]
  • Catalog: CAS COVID-19 Anti-Viral Candidate Compounds[7]
  • Isomeric SMILES: CC1([C@@H]2[C@H]1C@HC(=O)NC(CC3CCC3)C(=O)C(=O)N)CC@HC(=O)NC(CC3CCC3)C(=O)C(=O)N)C">[8]
  • Mass: 519.34207 dalton[9]
  • Medical condition treated: hepatitis C[10], liver cirrhosis[11]
  • World Health Organisation international non-proprietary name: boceprevir[12]
  • Subject has role: antiviral drug[13], bactericide[14]
  • Pregnancy category: US pregnancy category X[15]
  • Active ingredient in: Victrelis[16]
  • Defined daily dose: 2.4 g[17]
  • LiverTox likelihood score: LiverTox toxicity likelihood category E*[18]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [2] ↑ . wikidata.org.
  5. [6] ↑ . DrugBank. wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Drug Indications Extracted from FAERS. Retrieved . wikidata.org.
  10. [11] ↑ . Drug Indications Extracted from FAERS. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . ChEBI. wikidata.org.
  13. [14] ↑ . ChEBI. wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . ema.europa.eu. Retrieved . ema.europa.eu. Provenance: wikidata.org.
  16. [17] ↑ . whocc.no. whocc.no. Provenance: wikidata.org.
  17. [18] ↑ . LiverTox. Retrieved . ncbi.nlm.nih.gov. Provenance: wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). boceprevir. Retrieved November 4, 2026, from https://4ort.xyz/entity/boceprevir
MLA “boceprevir.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/boceprevir.
BibTeX @misc{4ortxyz_boceprevir_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{boceprevir}}, year = {2026}, url = {https://4ort.xyz/entity/boceprevir}, note = {Accessed: 2026-11-04}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 2d ago · Elivan da Silva · 2026-11-04 view diff on Wikidata ↗
    Claims rich → —
    "/* wbsetreference-add:2| */ ATC code: J05AP03, #temporary_batch_1793797550071"
  2. 20w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Defined daily dose → {'unit': 'Q41803', 'amount': '+2.4'}
    Instance of → group of stereoisomers
    Has use → medication
    LiverTox likelihood score → LiverTox toxicity likelihood category E*
    + 11 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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