Please click on the ID to see detailed information about each entry.
The total number entries retrieved from this search areID1043 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability>5% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1044 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~6% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1045 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~1.5% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1046 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~5% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1047 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~3% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1048 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~2% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1049 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~7% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1050 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~3% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1051 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability2% of applied dose | Tissue SampleStratum corneum of human breast skin | PUBMED ID22890441 |
ID1052 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~11% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1053 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~9% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1054 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~3% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1055 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~10% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1056 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~7% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1057 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~5% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1058 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~12% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1059 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability>4% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1060 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~4% of applied dose | Tissue SampleEpidermis of human breast skin | PUBMED ID22890441 |
ID1061 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability>36% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1062 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability>26% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1063 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~26% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1064 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability25% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1065 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability20% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1066 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~20% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1067 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~26% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1068 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability13% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1069 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability14% of applied dose | Tissue SampleDermis of human breast skin | PUBMED ID22890441 |
ID1070 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability9.5% of applied dose | Tissue SampleAcceptor compartment of Franz diffusion cell | PUBMED ID22890441 |
ID1071 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~7% of applied dose | Tissue SampleAcceptor compartment of Franz diffusion cell | PUBMED ID22890441 |
ID1072 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability>19% of applied dose | Tissue SampleAcceptor compartment of Franz diffusion cell | PUBMED ID22890441 |
ID1073 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability21% of applied dose | Tissue SampleAcceptor compartment of Franz diffusion cell | PUBMED ID22890441 |
ID1074 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability>8% of applied dose | Tissue SampleAcceptor compartment of Franz diffusion cell | PUBMED ID22890441 |
ID1075 | Sequenceβ-Ala-H | NameN-acetyl- L -carnosine | Nature of peptide or cargoAntioxidant | AssayFranz diffusion cell, HPLC | Tissue permeability~15% of applied dose | Tissue SampleAcceptor compartment of Franz diffusion cell | PUBMED ID22890441 |
ID1110 | SequenceYTSLIHSLIEESQNQQ EKNEQELLELDKWAS LWNWF | NameN-acetylated T20 | Nature of peptide or cargoFusion inhibitor | AssayReal-time PCR | Tissue permeabilityIC50 of 51.2 microM (230 ng/ml; 95% confidence interval, 198 to 267 ng/ml; n 8 independent experiments with 4 donor tissues) | Tissue SampleVaginal epithelial sheet | PUBMED ID19949052 |
ID1289 | SequenceGrGDIPASSKGGGGS rLLLLLLr | NameRGD peptide matrix | Nature of peptide or cargoActs as a temporary topical synthetic extracellular matrix that presents attachment sites for cells and substitutes for the damaged natural matrix and provides support for cell ingrowth into the ulcer site | AssayAt each visit, the ulcer was cleansed, debrided as needed, traced on acetate film for size determination, and photographed. Ulcer area was determined by computerized planimetry. Regression analysis was also done. | Tissue permeabilityMean percent ulcer closure at study endpoint in ulcers of varying baseline durations ~ 57% (32 patients) | Tissue SamplePatients were eligible for inclusion in the study if they presented with isolated full-thickness lower leg or ankle ulcers that did not involve bone or tendon and had persisted at least for one month. The peptide matrix is topically applied to the ulcers which were situated at the ankle | PUBMED ID8080985 |
ID1290 | SequenceGrGDIPASSKGGGGS rLLLLLLr | NameRGD peptide matrix | Nature of peptide or cargoActs as a temporary topical synthetic extracellular matrix that presents attachment sites for cells and substitutes for the damaged natural matrix and provides support for cell ingrowth into the ulcer site | AssayAt each visit, the ulcer was cleansed, debrided as needed, traced on acetate film for size determination, and photographed. Ulcer area was determined by computerized planimetry. Regression analysis was also done. | Tissue permeabilityMean percent ulcer closure at study endpoint in ulcers of varying baseline durations ~ 55% (23 patients) | Tissue SamplePatients were eligible for inclusion in the study if they presented with isolated full-thickness lower leg or ankle ulcers that did not involve bone or tendon and had persisted at least for one month. The peptide matrix is topically applied to the ulcers which were situated at the ankle | PUBMED ID8080985 |
ID1291 | SequenceGrGDIPASSKGGGGS rLLLLLLr | NameRGD peptide matrix | Nature of peptide or cargoActs as a temporary topical synthetic extracellular matrix that presents attachment sites for cells and substitutes for the damaged natural matrix and provides support for cell ingrowth into the ulcer site | AssayAt each visit, the ulcer was cleansed, debrided as needed, traced on acetate film for size determination, and photographed. Ulcer area was determined by computerized planimetry. Regression analysis was also done. | Tissue permeabilityMean percent ulcer closure at study endpoint in ulcers of varying baseline durations ~ 54% (21 patients) | Tissue SamplePatients were eligible for inclusion in the study if they presented with isolated full-thickness lower leg or ankle ulcers that did not involve bone or tendon and had persisted at least for one month. The peptide matrix is topically applied to the ulcers which were situated at the ankle | PUBMED ID8080985 |
ID1292 | SequenceGrGDIPASSKGGGGS rLLLLLLr | NameRGD peptide matrix | Nature of peptide or cargoActs as a temporary topical synthetic extracellular matrix that presents attachment sites for cells and substitutes for the damaged natural matrix and provides support for cell ingrowth into the ulcer site | AssayAt each visit, the ulcer was cleansed, debrided as needed, traced on acetate film for size determination, and photographed. Ulcer area was determined by computerized planimetry. Regression analysis was also done. | Tissue permeabilityMean percent ulcer closure at study endpoint in ulcers of varying baseline durations ~ 56% (20 patients) | Tissue SamplePatients were eligible for inclusion in the study if they presented with isolated full-thickness lower leg or ankle ulcers that did not involve bone or tendon and had persisted at least for one month. The peptide matrix is topically applied to the ulcers which were situated at the ankle | PUBMED ID8080985 |
ID1293 | SequenceGrGDIPASSKGGGGS rLLLLLLr | NameRGD peptide matrix | Nature of peptide or cargoActs as a temporary topical synthetic extracellular matrix that presents attachment sites for cells and substitutes for the damaged natural matrix and provides support for cell ingrowth into the ulcer site | AssayAt each visit, the ulcer was cleansed, debrided as needed, traced on acetate film for size determination, and photographed. Ulcer area was determined by computerized planimetry. Regression analysis was also done. | Tissue permeabilityMean percent ulcer closure at study endpoint in ulcers of varying baseline durations ~ 58% (16 patients) | Tissue SamplePatients were eligible for inclusion in the study if they presented with isolated full-thickness lower leg or ankle ulcers that did not involve bone or tendon and had persisted at least for one month. The peptide matrix is topically applied to the ulcers which were situated at the ankle | PUBMED ID8080985 |
ID1294 | SequenceGrGDIPASSKGGGGS rLLLLLLr | NameRGD peptide matrix | Nature of peptide or cargoActs as a temporary topical synthetic extracellular matrix that presents attachment sites for cells and substitutes for the damaged natural matrix and provides support for cell ingrowth into the ulcer site | AssayAt each visit, the ulcer was cleansed, debrided as needed, traced on acetate film for size determination, and photographed. Ulcer area was determined by computerized planimetry. Regression analysis was also done. | Tissue permeabilityMean percent ulcer closure at study endpoint in ulcers of varying baseline durations ~ 61% (14 patients) | Tissue SamplePatients were eligible for inclusion in the study if they presented with isolated full-thickness lower leg or ankle ulcers that did not involve bone or tendon and had persisted at least for one month. The peptide matrix is topically applied to the ulcers which were situated at the ankle | PUBMED ID8080985 |
ID1301 | SequenceSYSMEHFRWGKPV | Nameα-Melanocyte stimulating hormone (MSH) | Nature of peptide or cargoControls pigmentary changes in many vertebrates and melanin synthesis within epidermal melanocytes is responsible for melanin pigmentation of the skin, hair, and feathers in man, birds and other mammals. | AssayLight and electron microscopy | Tissue permeability10-7 and 10-8 concentrations turned yellow hair brown | Tissue SampleMelanotropin dose was applied on the shaved skin of C57BL/6AY mice which stimulated the yellow hair to turn yellow which was observed at other untouched areas proving systemic effect | PUBMED ID3684299 |
ID1302 | SequenceSYS-Nle-EHfRWGKPV | Name[Nle4, D-Phe7]-alpha-MSH | Nature of peptide or cargoThe analogue is superpotent, being 10- 1000 times more active than the native hormone | AssayLight and electron microscopy | Tissue permeability10-7 to 10-12 concentrations turned yellow hair brown | Tissue SampleMelanotropin dose was applied on the shaved skin of C57BL/6AY mice which stimulated the yellow hair to turn yellow which was observed at other untouched areas proving systemic effect | PUBMED ID3684299 |
ID1303 | SequenceNle-EHfRWGK | Name[Nle4, D-Phe7]-alpha-MSH4-11 | Nature of peptide or cargoNot mentioned | AssayLight and electron microscopy | Tissue permeability10-8 to 10-14 concentrations turned yellow hair brown | Tissue SampleMelanotropin dose was applied on the shaved skin of C57BL/6AY mice which stimulated the yellow hair to turn yellow which was observed at other untouched areas proving systemic effect | PUBMED ID3684299 |
ID1304 | SequenceNle-EHfRWG | Name[Nle4, D-Phe7]-alpha-MSH4-10 | Nature of peptide or cargoNot mentioned | AssayLight and electron microscopy | Tissue permeability10-8 to 10-14 concentrations turned yellow hair brown | Tissue SampleMelanotropin dose was applied on the shaved skin of C57BL/6AY mice which stimulated the yellow hair to turn yellow which was observed at other untouched areas proving systemic effect | PUBMED ID3684299 |
ID1306 | SequenceSYS-Nle-EHfRWGKPV | Name(Nle4, D-Phe7]-α-MSH | Nature of peptide or cargothe melanotropin analogs stimulated follicular eumelanogenesis when applied topically to the skin of mice | AssayElectron microscopy and Light microscopy | Tissue permeabilityConcentrations (10-7 M-10-15 M) induced the emergent hairs to become brown at the sites of application. | Tissue Sampledorsal trunk of mice (C57BL/6JA y) | PUBMED ID3624899 |
ID1307 | SequenceNle-EHfFRWGK | NameAc-[Nle4, D-Phe7]-α- MSH4–11-NH2 | Nature of peptide or cargothe melanotropin analogs stimulated follicular eumelanogenesis when applied topically to the skin of mice | AssayElectron microscopy and Light microscopy | Tissue permeabilityConcentrations (10-7 M-10-15 M) induced the emergent hairs to become brown at the sites of application. | Tissue Sampledorsal trunk of mice (C57BL/6JA y) | PUBMED ID3624899 |
ID1308 | SequenceNle-EH-FRWG | NameAc-[Nle4, D-Phe7]-α-MSH4–10-NH2 | Nature of peptide or cargothe melanotropin analogs stimulated follicular eumelanogenesis when applied topically to the skin of mice | AssayElectron microscopy and Light microscopy | Tissue permeabilityConcentrations (10-7 M-10-15 M) induced the emergent hairs to become brown at the sites of application. | Tissue Sampledorsal trunk of mice (C57BL/6JA y) | PUBMED ID3624899 |
ID1309 | SequenceSYSMEHFRWGKPV | Nameα-Melanocyte stimulating hormone (MSH) | Nature of peptide or cargoControls pigmentary changes in many vertebrates and melanin synthesis within epidermal melanocytes is responsible for melanin pigmentation of the skin, hair, and feathers in man, birds and other mammals. | AssayElectron microscopic examination | Tissue permeabilityMinimal effective dose=10-8to10-9M. It stimulated eumelanogenesis in all hair emerging from the areas previously plucked. | Tissue SamplePosterior dorsum of mice (C57BL/6JA y) | PUBMED ID3573985 |
ID1310 | SequenceSYS-Nle-EHfRWGKPV | Name(Nle4, D-Phe7)-a-MSH | Nature of peptide or cargoThe analogue is superpotent, being 10- 1000 times more active than the native hormone | AssayElectron microscopic examination | Tissue permeabilityMinimal effective dose=10-12M. It is transdermally delivered systemically to hair follicles throughout the body to induce follicular melanogenesis. Microscopic examination revealed eumelanin within hair bulbs by 24 hours after topical application of the analogue. | Tissue SamplePosterior dorsum of mice (C57BL/6JA y) | PUBMED ID3573985 |
ID1311 | SequenceSYS-Nle-EHfRWGKPV | Name[Nle4, D-Phe7]-alpha-MSH | Nature of peptide or cargoA superpotent(10-1000 times) analogue of alpha-melanocyte stimulating hormone, it causes a very long lasting stimulation of melanocytes in vitro and in vivo, its nonbiodegradeable and it is resistant to enzymatic inactivation by sera, brain enzymes or purified proteolytic enzymes. | AssayFrog Skin Bioassay | Tissue permeabilityPercent positive samples of transdermal delivery :65% (15/23) | Tissue SampleFull thickness skin samples (approximately 1 and a half" in diameter) were removed from the trunk area of either black or yellow adult C57BL/6JAy mice killed by cervical dislocation | PUBMED ID2845208 |