Target Validation Information | |||||
---|---|---|---|---|---|
Target ID | T67103 | ||||
Target Name | Integrin alpha-V | ||||
Target Type | Clinical Trial |
||||
Drug Potency against Target | Cyclo-[-Arg-Gly-Asp-Amp22-] | Drug Info | IC50 = 600 nM | [529343] | |
C[RGDf-(3R)-Carboxymorpholine] | Drug Info | IC50 = 21 nM | [529951] | ||
E[c(RGDyK)]2-PTX conjugate | Drug Info | IC50 = 134 nM | [527440] | ||
C(RGDfMeF) | Drug Info | IC50 = 19.81 nM | [528059] | ||
C(RGDfV) | Drug Info | IC50 = 600 nM | [528438] | ||
Ac-Asp-Arg-Leu-Asp-Ser-OH | Drug Info | IC50 = 25 nM | [529045] | ||
SB-265123 | Drug Info | IC50 = 2.9 nM | [527268] | ||
AcDRGDS | Drug Info | IC50 = 20 nM | [528659] | ||
Cyclo-[-Arg-Gly-Asp-Amp21-] | Drug Info | IC50 = 390 nM | [529343] | ||
C(RGDfF) | Drug Info | IC50 = 15.65 nM | [528059] | ||
Cypate-[(RGD)2-NH2]2 | Drug Info | IC50 = 104 nM | [528111] | ||
Cypate-[(RGD)4-NH2]2 | Drug Info | IC50 = 79.6 nM | [528111] | ||
Cypate-[(RGD)4-NH2]1 | Drug Info | IC50 = 25.9 nM | [528111] | ||
Cypate-[(RGD)3-NH2]2 | Drug Info | IC50 = 132 nM | [528111] | ||
C[RGDf-(S)-N-Me-alpha-TfmF] | Drug Info | IC50 = 7.7 nM | [528059] | ||
C[RGD-(S)-alpha-TfmfV] | Drug Info | IC50 = 10.03 nM | [528059] | ||
C-[-Arg-Gly-Asp-Acpca30-] | Drug Info | IC50 = 6.56 nM | [527884] | ||
C[-Arg-Gly-Asp-Acpca22-] | Drug Info | IC50 = 165.5 nM | [527884] | ||
C[-Arg-Gly-Asp-Acpca20-] | Drug Info | IC50 = 1300 nM | [527884] | ||
C[RGDf-(S,R)-alpha-Dfm-F] | Drug Info | IC50 = 5.5 nM | [528059] | ||
C[-Arg-Gly-Asp-Acpca19-] | Drug Info | IC50 = 411.5 nM | [527884] | ||
C[-Arg-Gly-Asp-Acpca36-] | Drug Info | IC50 = 4.56 nM | [527884] | ||
C[RGDf-(R)-alpha-TfmV] | Drug Info | IC50 = 42.8 nM | [528059] | ||
NAVPNLRGDLQVLAQKVART | Drug Info | IC50 = 1540 nM | [528633] | ||
Gly-Arg-Gly-Asp-Ser-Pro-Lys | Drug Info | IC50 = 210 nM | [525558] | ||
C[RGDf-(3S)-Carboxymorpholine] | Drug Info | IC50 = 157 nM | [529951] | ||
C-[-Arg-Gly-Asp-Acpca31-] | Drug Info | IC50 = 3.43 nM | [527884] | ||
CYCLORGDFV | Drug Info | IC50 = 9600 nM | [530622] | ||
ISONIPECOTAMIDE | Drug Info | IC50 = 45.7 nM | [527223] | ||
C[-Arg-Gly-Asp-Acpca34-] | Drug Info | IC50 = 29.6 nM | [527884] | ||
E[c(RGDyK)]2 | Drug Info | IC50 = 2.9 nM | [527440] | ||
SB-223245 | Drug Info | Ki = 2 nM | [534805] | ||
G(D-Pen)-G-H-R-G-D-L-R-C-A | Drug Info | IC50 = 5270 nM | [533606] | ||
C(-GRGDfL-) | Drug Info | IC50 = 100 nM | [529125] | ||
Gly-Arg-Gly-Asp-Ser | Drug Info | IC50 = 750 nM | [530479] | ||
Cypate-[(RGD)2-NH2]1 | Drug Info | IC50 = 730 nM | [528111] | ||
C[RGD-(R)-alpha-TfmfV] | Drug Info | IC50 = 72.7 nM | [528059] | ||
C[RGDf-(R)-alpha-TfmF] | Drug Info | IC50 = 93.5 nM | [528059] | ||
Cyclo(RGDfV) (control) | Drug Info | IC50 = 28.7 nM | [528111] | ||
Cyclo[RGDfK(cypate)] | Drug Info | IC50 = 63.9 nM | [528111] | ||
C[RGDf-(R)-N-Me-alpha-TfmF] | Drug Info | IC50 = 93.9 nM | [528059] | ||
C[RGDf-(S)-alpha-TfmF] | Drug Info | IC50 = 35.5 nM | [528059] | ||
C[-Arg-Gly-Asp-Acpca21-] | Drug Info | IC50 = 125.4 nM | [527884] | ||
C-[-Arg-Gly-Asp-Acpca32-] | Drug Info | IC50 = 0.59 nM | [527884] | ||
C-[-Arg-Gly-Asp-Acpca33-] | Drug Info | IC50 = 26 nM | [527884] | ||
Cypate-[(RGD)3-NH2]1 | Drug Info | IC50 = 481 nM | [528111] | ||
C[-Arg-Gly-Asp-Acpca35-] | Drug Info | IC50 = 13.1 nM | [527884] | ||
ST-1646 | Drug Info | IC50 = 0.9 nM | [529343] | ||
C[RGDf-(S)-alpha-TfmV] | Drug Info | IC50 = 3.4 nM | [528059] | ||
RGDechi | Drug Info | IC50 = 880 nM | [528215] | ||
C(Arg-Gly-Asp-D-Phe-Val) | Drug Info | IC50 = 680 nM | [528215] | ||
TR-14035 | Drug Info | IC50 = 414 nM | [528475] | ||
N-(3,5-dichlorophenyl)imidodicarbonimidic diamide | Drug Info | IC50 = 33.5 nM | [530779] | ||
References | |||||
Ref 529343 | J Med Chem. 2008 Mar 27;51(6):1771-82. Epub 2008 Feb 28.Discovery of subnanomolar arginine-glycine-aspartate-based alphaVbeta3/alphaVbeta5 integrin binders embedding 4-aminoproline residues. | ||||
Ref 529951 | Bioorg Med Chem. 2009 Feb 15;17(4):1542-9. Epub 2009 Jan 13.Morpholine-based RGD-cyclopentapeptides as alphavbeta3/alphavbeta5 integrin ligands: role of configuration towards receptor binding affinity. | ||||
Ref 527440 | J Med Chem. 2005 Feb 24;48(4):1098-106.Synthesis and biological evaluation of dimeric RGD peptide-paclitaxel conjugate as a model for integrin-targeted drug delivery. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528438 | Bioorg Med Chem Lett. 2006 Nov 15;16(22):5878-82. Epub 2006 Sep 18.Discovery of small molecule inhibitors of integrin alphavbeta3 through structure-based virtual screening. | ||||
Ref 529045 | Bioorg Med Chem. 2007 Dec 1;15(23):7380-90. Epub 2007 Aug 22.Synthesis and biological evaluation of non-peptide alpha(v)beta(3)/alpha(5)beta(1) integrin dual antagonists containing 5,6-dihydropyridin-2-one scaffolds. | ||||
Ref 527268 | Bioorg Med Chem Lett. 2004 Dec 6;14(23):5937-41.1,2,3,4-Tetrahydroquinoline-containing alphaVbeta3 integrin antagonists with enhanced oral bioavailability. | ||||
Ref 528659 | Bioorg Med Chem Lett. 2007 Apr 15;17(8):2329-33. Epub 2007 Jan 27.Inhibition of cancer cell adhesion by heterochiral Pro-containing RGD mimetics. | ||||
Ref 529343 | J Med Chem. 2008 Mar 27;51(6):1771-82. Epub 2008 Feb 28.Discovery of subnanomolar arginine-glycine-aspartate-based alphaVbeta3/alphaVbeta5 integrin binders embedding 4-aminoproline residues. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528633 | J Biol Chem. 2007 Mar 30;282(13):9657-65. Epub 2007 Jan 23.Structure-function analysis of Arg-Gly-Asp helix motifs in alpha v beta 6 integrin ligands. | ||||
Ref 525558 | J Med Chem. 1999 Aug 12;42(16):3033-40.N-Methylated cyclic RGD peptides as highly active and selective alpha(V)beta(3) integrin antagonists. | ||||
Ref 529951 | Bioorg Med Chem. 2009 Feb 15;17(4):1542-9. Epub 2009 Jan 13.Morpholine-based RGD-cyclopentapeptides as alphavbeta3/alphavbeta5 integrin ligands: role of configuration towards receptor binding affinity. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 530622 | J Med Chem. 2010 Jan 14;53(1):106-18.Antiangiogenic effect of dual/selective alpha(5)beta(1)/alpha(v)beta(3) integrin antagonists designed on partially modified retro-inverso cyclotetrapeptide mimetics. | ||||
Ref 527223 | Bioorg Med Chem Lett. 2004 Oct 18;14(20):5227-32.Piperidine-containing beta-arylpropionic acids as potent antagonists of alphavbeta3/alphavbeta5 integrins. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 527440 | J Med Chem. 2005 Feb 24;48(4):1098-106.Synthesis and biological evaluation of dimeric RGD peptide-paclitaxel conjugate as a model for integrin-targeted drug delivery. | ||||
Ref 534805 | Bioorg Med Chem Lett. 1998 Nov 17;8(22):3171-6.Discovery of an imidazopyridine-containing 1,4-benzodiazepine nonpeptide vitronectin receptor (alpha v beta 3) antagonist with efficacy in a restenosis model. | ||||
Ref 533606 | J Med Chem. 1994 Jan 7;37(1):1-8.Design and synthesis of novel cyclic RGD-containing peptides as highly potent and selective integrin alpha IIb beta 3 antagonists. | ||||
Ref 529125 | J Med Chem. 2007 Nov 29;50(24):5878-81. Epub 2007 Nov 1.Multiple N-methylation by a designed approach enhances receptor selectivity. | ||||
Ref 530479 | J Med Chem. 2009 Nov 26;52(22):7029-43.alphavbeta3 Integrin-targeting Arg-Gly-Asp (RGD) peptidomimetics containing oligoethylene glycol (OEG) spacers. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 528111 | J Med Chem. 2006 Apr 6;49(7):2268-75.Design, synthesis, and evaluation of near infrared fluorescent multimeric RGD peptides for targeting tumors. | ||||
Ref 527884 | J Med Chem. 2005 Dec 1;48(24):7675-87.Grafting aminocyclopentane carboxylic acids onto the RGD tripeptide sequence generates low nanomolar alphaVbeta3/alphaVbeta5 integrin dual binders. | ||||
Ref 529343 | J Med Chem. 2008 Mar 27;51(6):1771-82. Epub 2008 Feb 28.Discovery of subnanomolar arginine-glycine-aspartate-based alphaVbeta3/alphaVbeta5 integrin binders embedding 4-aminoproline residues. | ||||
Ref 528059 | J Med Chem. 2006 Mar 9;49(5):1808-17.Incorporation of the unusual C(alpha)-fluoroalkylamino acids into cyclopeptides: synthesis of arginine-glycine-aspartate (RGD) analogues and study of their conformational and biological behavior. | ||||
Ref 528215 | J Med Chem. 2006 Jun 1;49(11):3416-20.Novel and selective alpha(v)beta3 receptor peptide antagonist: design, synthesis, and biological behavior. | ||||
Ref 528215 | J Med Chem. 2006 Jun 1;49(11):3416-20.Novel and selective alpha(v)beta3 receptor peptide antagonist: design, synthesis, and biological behavior. | ||||
Ref 528475 | Bioorg Med Chem Lett. 2007 Jan 1;17(1):142-6. Epub 2006 Oct 10.2,6-Quinolinyl derivatives as potent VLA-4 antagonists. | ||||
Ref 530779 | J Med Chem. 2010 Jun 10;53(11):4332-53.Emerging targets in osteoporosis disease modification. |
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