ProForma 2.0
validated simple linear
FPRPGGGGNGDFEEIPEEYL
Record tools
Copy identifiers or export this single peptide record for a local research note.
Bivalirudin
65
Quality PepDiana 0–100 composite of sequence, source, activity, literature, and cross-database evidence completeness.
2
Source DBs
7
Activities
7
Source refs
1
Literature
0
Patents
Integrated record
Length
Molecular weight
Formula
Structure type
Synthesis
Chirality
Family
Gene
Residue composition
Physicochemical profile
Membrane affinity proxy
Solubility proxy
Net charge proxy -4
Binding interaction proxy
Versioned scientific descriptors
Legacy compatibility fields are materialized from the versioned PepDiana computed release; no separate source-reported property is available.
Molecular weight
2180.2851 Da
Molecular formula
C98H138N24O33
Theoretical pI
4.05
Net charge at pH 7
-4.2285
GRAVY
-0.985
Instability index
77.45
Aromaticity
0.15
Topological polar surface area
901.57 Ų
cLogP
-8.1164
Hydrogen-bond donors
28
Hydrogen-bond acceptors
29
Rotatable bonds
66
Method: PepDiana sequence/structure descriptor pipeline
Tool: Biopython+RDKit · Biopython 1.85; RDKit 2024.09.6
Calculated: 2026-06-20T11:01:38.358971+00:00
Assumptions: ph=7; termini=free N-terminus and free C-terminus for simple linear peptides; stereochemistry=standard L-amino acids; smiles_length_limit=200
ProForma 2.0
validated simple linear
FPRPGGGGNGDFEEIPEEYL
HELM 2.0
validated simple linear
PEPTIDE1{F.P.R.P.G.G.G.G.N.G.D.F.E.E.I.P.E.E.Y.L}$$$$V2.0
Canonical SMILES
validated
CCC(C)C(NC(=O)C(CCC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(Cc1ccccc1)NC(=O)C(CC(=O)O)NC(=O)CNC(=O)C(CC(N)=O)NC(=O)CNC(=O)CNC(=O)CNC(=O)CNC(=O)C1CCCN1C(=O)C(CCCNC(=N)N)NC(=O)C1CCCN1C(=O)C(N)Cc1ccccc1)C(=O)N1CCCC1C(=O)NC(CCC(=O)O)C(=O)NC(CCC(=O)O)C(=O)NC(Cc1ccc(O)cc1)C(=O)NC(CC(C)C)C(=O)O
Isomeric SMILES
validated
CC[C@H](C)[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(=O)O)NC(=O)CNC(=O)[C@H](CC(N)=O)NC(=O)CNC(=O)CNC(=O)CNC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)O
Follow-up research
Links open third-party resources with the current PepDiana sequence, record name, or chemistry notation as the initial query.
Research workflow
@misc{PEPDIA-INT-021088,
title = {Bivalirudin},
author = {{PepDiana Consortium}},
year = {2026},
howpublished = {PepDiana Multifunctional Peptide Database},
url = {http://127.0.0.1:3004/peptides/PEPDIA-INT-021088},
note = {Accessed from local PepDiana development build}
}Bivalirudin. (2026). PepDiana record PEPDIA-INT-021088. PepDiana Multifunctional Peptide Database. http://127.0.0.1:3004/peptides/PEPDIA-INT-021088
Integrated source-database annotations
| Stable record | Activity | Subtype | Value | Target | Assay method | Source |
|---|---|---|---|---|---|---|
| CTPDB_P021088_ACT_peptherdia_0000 | Clinical / Approved Drug | General Therapeutic | Not available in the current structured import | Unknown | Not reported by source | 9peptherdia / linked |
| CTPDB_P021088_ACT_thpdb_0001 | Clinical / Approved Drug | General Therapeutic | Not available in the current structured import | Unknown | Not reported by source | Th1006_10032_rec0thpdb / unavailable |
| CTPDB_P021088_ACT_thpdb_0002 | Clinical / Approved Drug | General Therapeutic | Not available in the current structured import | Unknown | Not reported by source | Th1006_10033_rec1thpdb / unavailable |
| CTPDB_P021088_ACT_thpdb_0003 | Clinical / Approved Drug | General Therapeutic | Not available in the current structured import | Unknown | Not reported by source | Th1006_10034_rec2thpdb / unavailable |
| CTPDB_P021088_ACT_thpdb_0004 | Clinical / Approved Drug | General Therapeutic | Not available in the current structured import | Unknown | Not reported by source | Th1006_10035_rec3thpdb / unavailable |
| CTPDB_P021088_ACT_thpdb_0005 | Clinical / Approved Drug | General Therapeutic | Not available in the current structured import | Unknown | Not reported by source | Th1006_10036_rec4thpdb / unavailable |
| CTPDB_P021088_ACT_thpdb_0006 | Clinical / Approved Drug | General Therapeutic | Not available in the current structured import | Unknown | Not reported by source | Th1006_10037_rec5thpdb / unavailable |
Provenance
fPRPGGGGNGDFEEIPEEYL
thpdb
Th1006_10032_rec0
FPRPGGGGNGDFEEIPEEYL
thpdb
Th1006_10033_rec1
FPRPGGGGNGDFEEIPEEYL
thpdb
Th1006_10034_rec2
FPRPGGGGNGDFEEIPEEYL
thpdb
Th1006_10035_rec3
FPRPGGGGNGDFEEIPEEYL
thpdb
Th1006_10036_rec4
FPRPGGGGNGDFEEIPEEYL
thpdb
Th1006_10037_rec5
FPRPGGGGNGDFEEIPEEYL
Citation trail
[{"text": "drugbank.com", "url": "https://go.drugbank.com/drugs/DB00006", "markdown": "[drugbank.com](https://go.drugbank.com/drugs/DB00006)"}, {"text": "medicines.org.uk", "url": "https://www.medicines.org.uk/emc/product/7229/smpc#gref", "markdown": "[medicines.org.uk](https://www.medicines.org.uk/emc/product/7229/smpc#gref)"}, {"text": "fda.gov", "url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2000/20873lbl.pdf", "markdown": "[fda.gov](https://www.accessdata.fda.gov/drugsatfda_doc
Audit surface
Integrated record last updated: 2026-04-15T00:59:21.345173+00:00
Modification summary
No structured modification annotations are available for this record.
{
"toxicity": [
{
"source_db": "thpdb",
"assay_method": "Based on a study by Gleason et al., the no observed adverse effect level (NOAEL) for bivalirudin administered to rats via Intravenous infusion over a 24-hour period, was 2000 mg/kg/24 h.",
"toxicity_type": "Toxicity"
},
{
"source_db": "thpdb",
"assay_method": "Based on a study by Gleason et al., the no observed adverse effect level (NOAEL) for bivalirudin administered to rats via Intravenous infusion over a 24-hour period, was 2000 mg/kg/24 h.",
"toxicity_type": "Toxicity"
},
{
"source_db": "thpdb",
"assay_method": "Based on a study by Gleason et al., the no observed adverse effect level (NOAEL) for bivalirudin administered to rats via Intravenous infusion over a 24-hour period, was 2000 mg/kg/24 h.",
"toxicity_type": "Toxicity"
},
{
"source_db": "thpdb",
"assay_method": "Based on a study by Gleason et al., the no observed adverse effect level (NOAEL) for bivalirudin administered to rats via Intravenous infusion over a 24-hour period, was 2000 mg/kg/24 h.",
"toxicity_type": "Toxicity"
},
{
"source_db": "thpdb",
"assay_method": "Based on a study by Gleason et al., the no observed adverse effect level (NOAEL) for bivalirudin administered to rats via Intravenous infusion over a 24-hour period, was 2000 mg/kg/24 h.",
"toxicity_type": "Toxicity"
},
{
"source_db": "thpdb",
"assay_method": "Based on a study by Gleason et al., the no observed adverse effect level (NOAEL) for bivalirudin administered to rats via Intravenous infusion over a 24-hour period, was 2000 mg/kg/24 h.",
"toxicity_type": "Toxicity"
}
]
}[
{
"source_db": "peptherdia",
"organism_name": "Unknown"
},
{
"source_db": "thpdb",
"organism_name": "Unknown"
}
][
{
"status": "Therapeutic",
"drug_name": "Bivalirudin",
"source_db": "peptherdia",
"indication": "For treatment of heparin-induced thrombocytopenia and for the prevention of thrombosis. Bivalirudin is indicated for use in patients undergoing percutaneous coronary intervention (PCI), in patients at moderate to high risk acute coronary syndromes due to unstable angina or non-ST segment elevation in whom a PCI is planned.",
"approval_year": 2000,
"approval_agency": "FDA",
"administration_route": "IV, IC"
}
]{
"status": "Therapeutic",
"drug_name": "Bivalirudin",
"source_db": "peptherdia",
"indication": "For treatment of heparin-induced thrombocytopenia and for the prevention of thrombosis. Bivalirudin is indicated for use in patients undergoing percutaneous coronary intervention (PCI), in patients at moderate to high risk acute coronary syndromes due to unstable angina or non-ST segment elevation in whom a PCI is planned.",
"approval_year": 2000,
"approval_agency": "FDA",
"administration_route": "IV, IC"
}