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PEPDIA-INT-010782

Gold

Enfuvirtide, ENF, T-20, Fuzeon, DP-178

85

Quality

9

Source DBs

72

Activities

19

Source refs

21

Literature

1

Patents

Integrated record

Sequence and molecular profile

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF
Indexed sequence36 aa
1YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

Length

36

Molecular weight

4450.89 Da

Formula

C202H298N50O64

Structure type

Linear

Synthesis

Synthetic

Chirality

L

Family

-

Gene

-

Residue composition

L
6
E
6
S
4
Q
4
N
3
W
3
I
2
K
2
Y
1
T
1
H
1
D
1

Physicochemical profile

Hydrophobic14

Membrane affinity proxy

Polar12

Solubility proxy

Charged10

Net charge proxy -4

Aromatic6

Binding interaction proxy

Versioned scientific descriptors

Physicochemical properties and standard representations

calculated sequence and structure

Reported properties

Legacy compatibility fields are materialized from the versioned PepDiana computed release; no separate source-reported property is available.

Computed properties

physchem-20260620

Molecular weight

4450.8237 Da

Molecular formula

C202H298N50O64

Theoretical pI

4.3007

Net charge at pH 7

-5.1377

GRAVY

-0.875

Instability index

62.65

Aromaticity

0.1389

Topological polar surface area

1894.02 Ų

cLogP

-14.9565

Hydrogen-bond donors

63

Hydrogen-bond acceptors

60

Rotatable bonds

150

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

Sequence representations

representations-20260620 · RDKit 2024.09.6

ProForma 2.0

validated simple linear

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

HELM 2.0

validated simple linear

PEPTIDE1{Y.T.S.L.I.H.S.L.I.E.E.S.Q.N.Q.Q.E.K.N.E.Q.E.L.L.E.L.D.K.W.A.S.L.W.N.W.F}$$$$V2.0

Canonical SMILES

validated

CCC(C)C(NC(=O)C(CC(C)C)NC(=O)C(CO)NC(=O)C(Cc1c[nH]cn1)NC(=O)C(NC(=O)C(CC(C)C)NC(=O)C(CO)NC(=O)C(NC(=O)C(N)Cc1ccc(O)cc1)C(C)O)C(C)CC)C(=O)NC(CCC(=O)O)C(=O)NC(CCC(=O)O)C(=O)NC(CO)C(=O)NC(CCC(N)=O)C(=O)NC(CC(N)=O)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(=O)O)C(=O)NC(CCCCN)C(=O)NC(CC(N)=O)C(=O)NC(CCC(=O)O)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(=O)O)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(CCC(=O)O)C(=O)NC(CC(C)C)C(=O)NC(CC(=O)O)C(=O)NC(CCCCN)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(C)C(=O)NC(CO)C(=O)NC(CC(C)C)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(CC(N)=O)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(Cc1ccccc1)C(=O)O

Isomeric SMILES

validated

CC[C@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@@H](C)O)[C@@H](C)CC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(=O)O

Follow-up research

External analysis tools

Research workflow

Citation and local history

BibTeX

@misc{PEPDIA-INT-010782,
  title = {Enfuvirtide, ENF, T-20, Fuzeon, DP-178},
  author = {{PepDiana Consortium}},
  year = {2026},
  howpublished = {PepDiana Multifunctional Peptide Database},
  url = {http://127.0.0.1:3004/peptides/PEPDIA-INT-010782},
  note = {Accessed from local PepDiana development build}
}

APA-style note

Enfuvirtide, ENF, T-20, Fuzeon, DP-178. (2026). PepDiana record PEPDIA-INT-010782. PepDiana Multifunctional Peptide Database. http://127.0.0.1:3004/peptides/PEPDIA-INT-010782

This record is saved to local recent-view history so it can reappear on the peptide browser page.

Integrated source-database annotations

Biological activity (72 records)

Stable recordActivitySubtypeValueTargetAssay methodSource
CTPDB_P010782_ACT_avpdb_0000AntiviralGeneral AntiviralHighFeline leukemia virusELISAAVPdb_AVP1136avpdb / unavailable
CTPDB_P010782_ACT_camp_0008Antiviral-Not available in the current structured importUnknownNot reported by sourceCAMPSQ11362camp / linked
CTPDB_P010782_ACT_dbaasp_0009Antimicrobial-0.006 µg/mlHIV-1 IIIBNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0010Antimicrobial-0.05 µg/mlHIV-1 098Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0011Antimicrobial-0.526 µg/mlHIV-1 098-T20Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0012Antimicrobial-54.958 µg/mlHIV-1 098-T1249Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0013Antimicrobial-47.822 µg/mlHIV-1 098-T651Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0014Antimicrobial-0.015±0.001 µMHIV-1 NL4-3Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0015Antimicrobial-0.0024±0.0006 µMHIV-1 NL4-3 D36GNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0016Antimicrobial-0.023±0.008 µMHIV-1 NL4-3 D36G/V38ANot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0017Antimicrobial-0.049±0.01 µMHIV-1 NL4-3 D36G/N43DNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0018Antimicrobial-0.084±0.016 µMHIV-1 NL4-3 D36G/N43D/S138ANot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0019Antimicrobial-0.0034±0.0006 µMHIV-1 NL4-3 D36G/N126KNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0020Antimicrobial-0.39±0.155 µMHIV-1 NL4-3 DelV4/D36G/I37K/N126K/L204INot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0021Antimicrobial-0.0024±0.0006 µMHIV-1Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0022Antimicrobial-0.023±0.0082 µMHIV-1 NL4-3 V38ANot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0023Antimicrobial-0.049±0.01 µMHIV-1 NL4-3 N43DNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0024Antimicrobial-0.084±0.016 µMHIV-1 NL4-3 N43D/S138ANot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0025Antimicrobial-0.0718 µMHIV-1 IIIBNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0026Antimicrobial-0.091 µMHIV-1 IIIBNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0027Antimicrobial-0.0705 µMHIV-1 BaLNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0028Antimicrobial-0.0204-0.0462 µMHIV-1Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0029Antimicrobial-0.0071-0.0293 µMHIV-1 PsVNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0030Antimicrobial-0.0553 µMHIV-1 9489Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0031Antimicrobial->0.5 µMHIV-1 NL4-3 V38ANot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0032Antimicrobial-0.00253 µMHIV-1Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0033Antimicrobial-0.118 µMHIV-1 IIIBNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0034Antimicrobial-0.02297 µMHIV-1 IIIBNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0035Antimicrobial-0.01643 µMHIV-1 BaLNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0036Antimicrobial-0.0129-0.0422 µMHIV-1Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0037Antimicrobial-0.0266-0.055 µMHIV-1 PsVNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0038Antimicrobial->0.5 µMHIV-1 NL4-3 V38ANot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0039Antimicrobial->0.5 µMHIV-1 NL4-3 D36GNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0040Antimicrobial-0.37 µg/mlHIV-1 NL4-3Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0041Antimicrobial-0.09 µg/mlHIV-1 JRCSFNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0042Antimicrobial-0.02-3.58 µg/mlHIV-1 PsVNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0043Antimicrobial-0.341508 µMHIV-2 RODNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0044Antimicrobial-0.630633 µMHIV-2Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0045Antimicrobial-0.03473667 µMHIV-1 PsVNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0046Antimicrobial-0.05302764 µMHIV-1 NL4-3Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0047Antimicrobial-0.00446808 µMHIV-1 JRCSFNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0048Antimicrobial-0.008564 µMHIV-1 NL4-3 D36GNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0049Antimicrobial-0.169333 µMHIV-1 NL4-3Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0050Antimicrobial-0.317333-7.901 µMHIV-1 NL4-3Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0051Antimicrobial-0.00863144 µMHIV-1Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0052Antimicrobial-0.53433-0.915516 µMSimian immunodeficiency virus (SIV)Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0053Antimicrobial-0.0259051 µMHIV-1 HxB2Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0054Antimicrobial-0.008564 µMHIV-1 NL4-3 D36G PsVNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0055Antimicrobial-0.04738667 µMHIV-1 NL4-3Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0056Antimicrobial-0.00296833 µMHIV-1 JRCSFNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0057Antimicrobial-0.00116333-0.031310 µMHIV-1Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0058Antimicrobial-0.02995009 µMHIV-1Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0059AnticancerCytotoxic148.73 µMHuman adenocarcinoma TZM-blNot reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dbaasp_0060AnticancerCytotoxic167.25 µMHuman T cell leukemia MT-4Not reported by sourceDBAASPS_6056_chain0dbaasp / linked
CTPDB_P010782_ACT_dramp_0061Antimicrobial-Not available in the current structured importUnknownNot reported by sourceDRAMP15987dramp / linked
CTPDB_P010782_ACT_dramp_0062Antiviral-Not available in the current structured importUnknownNot reported by sourceDRAMP15987dramp / linked
CTPDB_P010782_ACT_dramp_0063AntiviralAnti-HIVNot available in the current structured importUnknownNot reported by sourceDRAMP18181dramp / linked
CTPDB_P010782_ACT_hipdb_0005AntiviralAnti-HIVHighHIVNot reported by sourceHIPdb_HIP1087hipdb / unavailable
CTPDB_P010782_ACT_hipdb_0001AntiviralAnti-HIV222.0 nMHIVNot reported by sourceHIPdb_HIP1118hipdb / unavailable
CTPDB_P010782_ACT_hipdb_0003AntiviralAnti-HIV0.6 ng/mlHIVNot reported by sourceHIPdb_HIP876hipdb / unavailable
CTPDB_P010782_ACT_hipdb_0002AntiviralAnti-HIVMediumHIVNot reported by sourceHIPdb_HIP877hipdb / unavailable
CTPDB_P010782_ACT_hipdb_0004AntiviralAnti-HIV2.4±0.6 nM(fold)HIVNot reported by sourceHIPdb_HIP878hipdb / unavailable
CTPDB_P010782_ACT_hipdb_0006AntiviralAnti-HIV0.05 μg/mlHIVNot reported by sourceHIPdb_HIP879hipdb / unavailable
CTPDB_P010782_ACT_hipdb_0007AntiviralAnti-HIV95.0%HIVNot reported by sourceHIPdb_HIP958hipdb / unavailable
CTPDB_P010782_ACT_peptherdia_0064Clinical / Approved DrugGeneral TherapeuticNot available in the current structured importUnknownNot reported by source22peptherdia / linked
CTPDB_P010782_ACT_satpdb_0065Antiviral-Not available in the current structured importUnknownNot reported by sourcesatpdb10220satpdb / linked
CTPDB_P010782_ACT_satpdb_0066Antimicrobial-Not available in the current structured importUnknownNot reported by sourcesatpdb10220satpdb / linked
CTPDB_P010782_ACT_thpdb_0067Clinical / Approved DrugGeneral TherapeuticNot available in the current structured importUnknownNot reported by sourceTh1088_10478_rec0thpdb / unavailable
CTPDB_P010782_ACT_thpdb_0068Clinical / Approved DrugGeneral TherapeuticNot available in the current structured importUnknownNot reported by sourceTh1088_10479_rec1thpdb / unavailable
CTPDB_P010782_ACT_thpdb_0069Clinical / Approved DrugGeneral TherapeuticNot available in the current structured importUnknownNot reported by sourceTh1088_10480_rec2thpdb / unavailable
CTPDB_P010782_ACT_topicalpdb_0070Wound HealingSkin PenetratingNot available in the current structured importUnknownInduced a 50% inhibition of HIV-1JRCSF genomic integration in leukocytes residing within the vaginal epithelium (IC50) was 0.153 microM (0.687 ng/ml; 95% confidence interval, 0.563 to 0.84 ng/ml; n=7 independent experiments with 4 donor tissues.; Real-time PCR; ex vivo1109topicalpdb / linked
CTPDB_P010782_ACT_topicalpdb_0071Wound HealingSkin PenetratingNot available in the current structured importUnknownIC50 of 51.2 microM (230 ng/ml; 95% confidence interval, 198 to 267 ng/ml; n 8 independent experiments with 4 donor tissues); Real-time PCR; ex vivo1110topicalpdb / linked

Provenance

Source database records (19)

Source-specific sequence or modification context. One or more source records use a sequence notation that differs from the canonical backbone. Open each raw sequence before interpreting stereochemistry, terminal groups, or non-standard residues.

avpdb

AVPdb_AVP1136

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

hipdb

HIPdb_HIP1118

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

hipdb

HIPdb_HIP877

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

hipdb

HIPdb_HIP876

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

hipdb

HIPdb_HIP878

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

hipdb

HIPdb_HIP1087

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

hipdb

HIPdb_HIP879

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

hipdb

HIPdb_HIP958

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

camp

CAMPSQ11362

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

dbaasp

DBAASPS_6056_chain0

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

dramp

DRAMP15987

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

dramp

DRAMP18181

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

peptherdia

22

Raw sequence

Ac-YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

satpdb

satpdb10220

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

thpdb

Th1088_10478_rec0

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

thpdb

Th1088_10479_rec1

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

thpdb

Th1088_10480_rec2

Raw sequence

YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF

topicalpdb

1109

Raw sequence

YTSLIHSLIEESQNQQ EKNEQELLELDKWAS LWNWF

topicalpdb

1110

Raw sequence

YTSLIHSLIEESQNQQ EKNEQELLELDKWAS LWNWF

Citation trail

Literature (21 records)

In vitro inhibition of feline leukaemia virus infection by synthetic peptides derived from the transmembrane domain.

Boenzli E, Robert-Tissot C, Sabatino G, Cattori V, Meli ML, Gutte B, Rovero P, Flynn N, Hofmann-Lehmann R, Lutz H.

Antivir Ther2011PMID 21900723

{"pubmed_id": "22235115.0", "paper": "Trimeric, coiled-coil extension on peptide fusion inhibitor of HIV-1 influences selection of resistance pathways.", "authors": "Zhuang M, Wang W, De Feo CJ, Vassell R, Weiss CD.", "reference": "J Biol Chem. 2012 Mar 9;287(11):8297-309. Epub 2012 Jan 10."}

{"pubmed_id": "22235115.0", "paper": "Trimeric, coiled-coil extension on peptide fusion inhibitor of HIV-1 influences selection of resistance pathways.", "authors": "Zhuang M, Wang W, De Feo CJ, Vassell R, Weiss CD.", "reference": "J Biol Chem. 2012 Mar 9;287(11):8297-309. Epub 2012 Jan 10."}

--

{"pubmed_id": "US7919101", "paper": "Highly potent synergistic combinations of human immunodeficiency virus (HIV) fusion inhibitors", "authors": "Shibo Jiang, Chungen Pan", "reference": "New York Blood Center"}

{"pubmed_id": "US7919101", "paper": "Highly potent synergistic combinations of human immunodeficiency virus (HIV) fusion inhibitors", "authors": "Shibo Jiang, Chungen Pan", "reference": "New York Blood Center"}

--

{"pubmed_id": "US6861059", "paper": "Methods and compositions for treatment of HIV-1 infection using antiviral compounds in simultaneous or sequential combinations", "authors": "M. Ross Johnson, Dennis Michael Lambert", "reference": "Trimeris, Inc."}

{"pubmed_id": "US6861059", "paper": "Methods and compositions for treatment of HIV-1 infection using antiviral compounds in simultaneous or sequential combinations", "authors": "M. Ross Johnson, Dennis Michael Lambert", "reference": "Trimeris, Inc."}

--

{"pubmed_id": "19073606.0", "paper": "Design of peptide-based inhibitors for human immunodeficiency virus type 1 strains resistant to T-20.", "authors": "Izumi K, Kodama E, Shimura K, Sakagami Y, Watanabe K, Ito S, Watabe T, Terakawa Y, Nishikawa H, Sarafianos SG, Kitaura K, Oishi S, Fujii N, Matsuoka M.", "reference": "J Biol Chem. 2009 Feb 20;284(8):4914-20. Epub 2008 Dec 10."}

{"pubmed_id": "19073606.0", "paper": "Design of peptide-based inhibitors for human immunodeficiency virus type 1 strains resistant to T-20.", "authors": "Izumi K, Kodama E, Shimura K, Sakagami Y, Watanabe K, Ito S, Watabe T, Terakawa Y, Nishikawa H, Sarafianos SG, Kitaura K, Oishi S, Fujii N, Matsuoka M.", "reference": "J Biol Chem. 2009 Feb 20;284(8):4914-20. Epub 2008 Dec 10."}

--

{"pubmed_id": "17210123.0", "paper": "Inhibition of HIV-1 infection by synthetic peptides derived CCR5 fragments.", "authors": "Imai M, Baranyi L, Okada N, Okada H.", "reference": "Biochem Biophys Res Commun. 2007 Feb 23;353(4):851-6. Epub 2006 Dec 21."}

{"pubmed_id": "17210123.0", "paper": "Inhibition of HIV-1 infection by synthetic peptides derived CCR5 fragments.", "authors": "Imai M, Baranyi L, Okada N, Okada H.", "reference": "Biochem Biophys Res Commun. 2007 Feb 23;353(4):851-6. Epub 2006 Dec 21."}

--

{"pubmed_id": "17640899.0", "paper": "Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.", "authors": "Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK.", "reference": "Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12772-7. Epub 2007 Jul 19."}

{"pubmed_id": "17640899.0", "paper": "Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.", "authors": "Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK.", "reference": "Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12772-7. Epub 2007 Jul 19."}

--

{"pubmed_id": "11222732.0", "paper": "Membrane-anchored peptide inhibits human immunodeficiency virus entry.", "authors": "Hildinger M, Dittmar MT, Schult-Dietrich P, Fehse B, Schnierle BS, Thaler S, Stiegler G, Welker R, von Laer D.", "reference": "J Virol. 2001 Mar;75(6):3038-42."}

{"pubmed_id": "11222732.0", "paper": "Membrane-anchored peptide inhibits human immunodeficiency virus entry.", "authors": "Hildinger M, Dittmar MT, Schult-Dietrich P, Fehse B, Schnierle BS, Thaler S, Stiegler G, Welker R, von Laer D.", "reference": "J Virol. 2001 Mar;75(6):3038-42."}

--

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 17640899

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 19114674

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 19073606

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 27795416

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 31932193

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 31805154

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 31228294

Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtide-resistant virus.

Dwyer JJ, Wilson KL, Davison DK, Freel SA, Seedorff JE, Wring SA, Tvermoes NA, Matthews TJ, Greenberg ML, Delmedico MK

Proc Natl Acad Sci U S A2007PMID 30867304

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--

IP evidence

Patents (1)

US 20100261876

dramp

Audit surface

Raw annotations and release metadata

Integrated record last updated: 2026-04-15T00:59:13.225027+00:00

Modification summary

No structured modification annotations are available for this record.

ADMET
{
  "toxicity": [
    {
      "unit": "µM",
      "value": "187.28",
      "source_db": "dbaasp",
      "assay_method": "50% Cytotoxicity",
      "toxicity_type": "Cytotoxic",
      "target_cellline": "Human embryonic kidney HEK293T cells"
    },
    {
      "unit": "µM",
      "value": "75.24",
      "source_db": "dbaasp",
      "assay_method": "50% Cytotoxicity",
      "toxicity_type": "Cytotoxic",
      "target_cellline": "Human PBMC"
    }
  ]
}
Source metadata
[
  {
    "source_db": "avpdb",
    "organism_name": "Unknown"
  },
  {
    "source_db": "hipdb",
    "organism_name": "Unknown"
  },
  {
    "source_db": "camp",
    "organism_name": "Unknown"
  },
  {
    "source_db": "dbaasp",
    "organism_name": "Unknown"
  },
  {
    "source_db": "dramp",
    "organism_name": "Unknown"
  },
  {
    "source_db": "peptherdia",
    "organism_name": "Unknown"
  },
  {
    "source_db": "satpdb",
    "organism_name": "Unknown"
  },
  {
    "source_db": "thpdb",
    "organism_name": "Unknown"
  },
  {
    "source_db": "topicalpdb",
    "organism_name": "Unknown"
  }
]
Structure metadata
{
  "source_db": "satpdb",
  "dssp_states": "CHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHC"
}
Clinical trials
[
  {
    "status": "Therapeutic",
    "drug_name": "Enfuvirtide",
    "source_db": "peptherdia",
    "indication": "Antiretroviral drug used in combination therapy for the treatment of HIV-1/AIDS.",
    "approval_year": 2003,
    "approval_agency": "FDA-EMA",
    "administration_route": "SC"
  }
]
Approved drug annotations
{
  "status": "Therapeutic",
  "drug_name": "Enfuvirtide",
  "source_db": "peptherdia",
  "indication": "Antiretroviral drug used in combination therapy for the treatment of HIV-1/AIDS.",
  "approval_year": 2003,
  "approval_agency": "FDA-EMA",
  "administration_route": "SC"
}