KLTWQELYQLKYKGI

Product Name
VEGF mimicking peptide: KLTWQELYQLKYKGI; Related products KQLLWIRSGDRPWYTS; Ac-LTYQDLLQLQY-{D-Arg}-NH2
Product Quantity
4mg
Catalog Number
LT6116
Molecular Weight
1952.3
Sequence
Ac-KLTWQELYQLKYKGI-NH2
Product Description

The peptide sequence KLTWQELYQLKYKGI(QK) is a VEGF mimicking peptide, binds to the VEGF receptors and competes with VEGF. KLTWQELYQLKYKGI is active in gastric ulcer healing in rodents when administered either orally or systemically. KLTWQELYQLKYKGI shows the ability to induce capillary formation and organization in vitro

Functions

This peptide is involved in protein interactions and signaling pathways that can influence immune modulation. Peptides like this often serve as critical fragments in the study of epitopes—the part of an antigen molecule to which an antibody attaches itself, making it valuable in immunological studies and vaccine design.

Applications in Research and Drug Studies

  • Immunology: The peptide may serve as an epitope for T-cell activation studies. Understanding its role in the immune system helps in developing peptide-based vaccines and therapeutic agents for immune diseases or cancers.
  • Drug Development: Peptides like this one are being explored for their potential as vaccine components or immunomodulatory agents, which can help in creating treatments that harness the body’s immune response more effectively.
  • Therapeutic Targeting: Similar peptides are used to target specific proteins in therapeutic studies, helping to design drugs that can better regulate immune responses or inhibit harmful cellular activity in diseases such as cancer.

Role in Drug Studies

KLTWQELYQLKYKGI may be investigated in preclinical models to assess its ability to induce an immune response, making it a candidate for cancer immunotherapy or vaccine formulations. Research shows that peptide-based vaccines can target tumor antigens and other pathogens by stimulating the immune system, especially T-cells, against diseases.

The versatility and specificity of such peptides ensure their growing importance in biomedical research, drug development, and therapeutic interventions.

Structure-based designed peptides targeting VEGF/VEGFRs.

Peptide Sequence Target Mimicking  Affinity Ref.
- NGIDFNRDKFLFL VEGF VEGFR-2 - []
α/β-VEGF-1 V(β-Val)NK(β3-Phe)NKE(ACPC)CN
(APC)RAIE(Aib)ALDPNL NDQQFH
(Aib)KIW(APC)II(APC)DC 
VEGF Z-VEGF
(VEGF affibody)
Ki = 0.11 μM []
- YY(Abu)AARAWSPYSSTVDAGDFRYWGQ-amide  VEGF Nd42 (anti-VEGF nanobody) KA = 51 × 109 M []
Aib2 V(Aib)PNCDIHV(nL)WEWECFERL  VEGF V114* peptide KD = 4 nM []
Kv114* K(Aib)KKCDIHV(nL)WEWECFERL  VEGF V114* peptide KD = 540 nM []
QK Ac-KLTWQELYQLKYKGI-amide VEGFR1/R2 α1 VEGF-A KD = 64 μM []
MA Ac-KLTWMELYQLAYKGI-amide VEGFR1/R2 α1 VEGF-A KD = 46 μM []
#29 Ac-SSEEFARNWAAIN-amide VEGFR1 α1 VEGF-A IC50 = 0.05 μM []
VGB1 CSWIDVYTRATCQPRPL VEGFR1/R2 α1 VEGF-B - []
Vefin7 KAVSWVDVYTAAT-scaffold  VEGFR1 α1 VEGF-B KD = 0.167 μM []
#16 Ac-EV-cycle(NHCO)3,7[EKFM(O2) K]
VYQRSY-amide
VEGFR1 α1 Vammin IC50 = 36 μM []
#5 Ac-W(αMeAsp)N(αMeAsp)WR(Api)TW-amide  VEGFR1/R2 α1 VEGF-C - []
#6 Ac-(Api)WDN (αMeAsp)WR(Api)TW-amide  VEGFR1/R2 α1 VEGF-C - []
#14 CFQEYPDEIEYICK-amide VEGFR1 L1 VEGF-A IC50 = 50.4 μM []
#18 Ac-CTVELMGTVAKQLVPC-amide VEGFR1 L1 VEGF-B IC50 = 10.4 μM []
#19 CSEYPSEVEHMCS-amide VEGFR1 L1 PlGF IC50 = 56.0 μM []
#2 Ac-CNDEGLEC-amide VEGFR-1 L2 VEGF-A - []
Cyclo-VEGI Cycle(fPQIMRIKPHQGQHIGE) VEGFR1/R2 L3 VEGF-A IC50 = 0.7 μM []
#7 Ac-M-cycle(CH2NHCOCH2)2,10 [GIKPHQGQG]I-amide VEGFR1 L3 VEGF-A IC50 = 93.2 μM []
#8 Acetyl-M(aGly)GIKPHQQ(aGly)I-amide  VEGFR1 L3 VEGF-A IC50 = 42.3 μM []
VEGF-P3CYC Acetyl-ITMQCGIHQGQHPKIRMIC
EMSF-amide
VEGFR2 L3 VEGF-A KD = 11 nM []
HPLW KQLLWIRSGDRPWYYTS VEGFR1/R2 L3 PlGF KD = 32 μM []
HPLC KQCLWIRSGDRPWYCTS VEGFR1/R2 L3 PlGF - []
HPLW2 Ac-KQLL(Bpg)IRSGDRP(OrnN3) YWTS-amide  VEGFR1/R2 L3 PlGF - []
PLGF2 QLLKIRSHDRPSYVE-amide VEGFR1 L3 PlGF KD = 86 μM []
C1C12W3W10 CRWNPRTQSWKC VEGFR2 L3 Vammin - []
#7 c[YYDEGLEE]-amide VEGFR1 L2/α1 VEGF-A IC50 = 39.9 μM []
#3 c[YKDEGLEE]-NHCH2CH2Ph(3,4-diOH) VEGFR1 L2/α1 VEGF-A IC50 = 196 μM []
VG3F KFMDVYQRSY(Ahx)elGedncs(Ahx)ECRPK-amide  VEGFR1 α1/L2/L3 VEGF-A IC50 = 52 μM []
EP6 Ac-E(C-7Ahp-QIMRIKPHQGQHIGET
S)KFMDVYQLKYKGI-amide 
VEGFR1/R2 α1/L3 VEGF-A KD = 139 μM []
VGB CIKPHQGQHICNDE VEGFR1/R2 L2/L3 VEGF-A - []
VGB4 KQLVIKPHGQILMIRYPSSQLEM VEGFR1/R2 L1/L2 VEGF-B + L3 VEGF-A - []

Reference: Di Stasi R, De Rosa L, D'Andrea LD. Structure-Based Design of Peptides Targeting VEGF/VEGFRs. Pharmaceuticals (Basel). 2023 Jun 7;16(6):851. doi: 10.3390/ph16060851. PMID: 37375798; PMCID: PMC10302803.

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