CJC-1295 (no DAC) is also known as Modified GRF 1-29 or Mod GRF (1-29). It is a synthetic peptide analog of the first 29 amino acids of natural growth hormone-releasing hormone. GHRH is also called GRF in research literature.
$45.00
7 in stock
7 in stock
| Property | Details |
|---|---|
| Peptide Name | CJC-1295 (No DAC) |
| Alternative Name | Modified GRF (1-29), Mod GRF 1-29 |
| Peptide Type | Synthetic GHRH analog |
| Amino Acid Length | 29 |
| Peptide Sequence | Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-NH₂ |
| Molecular Formula | C₁₅₂H₂₅₂N₄₄O₄₂ |
| Molecular Weight | Approximately 3,367.95 Da |
| CAS Number | 863288-34-0 |
| C-Terminal Modification | Amidation (-NH₂) |
| DAC Modification | Absent |
| Research Target | Growth hormone-releasing hormone (GHRH) receptor |
| Position | Original Amino Acid | Modified Amino Acid | Research Significance |
|---|---|---|---|
| 2 | L-Alanine | D-Alanine (D-Ala) | Increases resistance to DPP-IV enzymatic cleavage |
| 8 | Asparagine (Asn) | Glutamine (Gln) | Reduces susceptibility to asparagine-related degradation |
| 15 | Glycine (Gly) | Alanine (Ala) | Structural modification investigated for its effects on peptide bioactivity |
| 27 | Methionine (Met) | Leucine (Leu) | Reduces susceptibility to methionine oxidation |
This compound is intended for laboratory research use only. It is not intended for human or animal consumption, or for use in diagnostic or therapeutic procedures.
| Molecular Formula | C152H252N44O42 |
| Molecular Weight | 3367.9 g/mol |
| Monoisotopic Mass | 3365.8935782 Da |
| Polar Surface Area | 1450 Ų |
| Complexity | 7710 |
| XLogP | -10.7 |
| Heavy Atom Count | 238 |
| Hydrogen Bond Donors | 52 |
| Hydrogen Bond Acceptors | 48 |
| Rotatable Bonds | 118 |
| CID | 91976842 |
| InChI | InChI=1S/C152H252N44O42/c1-22-79(15)118(194-125(214)84(20)171-135(224)107(68-115(206)207)181-124(213)81(17)169-126(215)91(155)65-87-41-45-89(201)46-42-87)147(236)189-106(66-86-34-25-24-26-35-86)141(230)196-120(85(21)200)149(238)180-99(51-54-114(158)205)132(221)190-111(72-199)145(234)185-105(67-88-43-47-90(202)48-44-88)140(229)178-96(40-33-59-168-152(164)165)128(217)177-94(37-28-30-56-154)133(222)193-117(78(13)14)146(235)187-100(60-73(3)4)134(223)170-82(18)123(212)175-97(49-52-112(156)203)130(219)183-103(63-76(9)10)138(227)191-109(70-197)143(232)172-83(19)122(211)174-95(39-32-58-167-151(162)163)127(216)176-93(36-27-29-55-153)129(218)182-102(62-75(7)8)137(226)184-101(61-74(5)6)136(225)179-98(50-53-113(157)204)131(220)186-108(69-116(208)209)142(231)195-119(80(16)23-2)148(237)188-104(64-77(11)12)139(228)192-110(71-198)144(233)173-92(121(159)210)38-31-57-166-150(160)161/h24-26,34-35,41-48,73-85,91-111,117-120,197-202H,22-23,27-33,36-40,49-72,153-155H2,1-21H3,(H2,156,203)(H2,157,204)(H2,158,205)(H2,159,210) |
| InChIKey | XOZMWINMZMMOBR-UHFFFAOYSA-N |
| IUPAC Name: | 4-[[1-[[1-[[1-[[1-[[5-amino-1-[[1-[[1-[[1-[[6-amino-1-[[1-[[1-[[1-[[5-amino-1-[[1-[[1-[[1-[[1-[[6-amino-1-[[1-[[1-[[5-amino-1-[[1-[[1-[[1-[[1-[(1-amino-5-carbamimidamido-1-oxopentan-2-yl)amino]-3-hydroxy-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-3-carboxy-1-oxopropan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1-oxohexan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1-oxohexan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-[2-[[2-amino-3-(4-hydroxyphenyl)propanoyl]amino]propanoylamino]-4-oxobutanoic acid |
| IUPAC Name: | CCC(C)C(C(=O)NC(CC1=CC=CC=C1)C(=O)NC(C(C)O)C(=O)NC(CCC(=O)N)C(=O)NC(CO)C(=O)NC(CC2=CC=C(C=C2)O)C(=O)NC(CCCNC(=N)N)C(=O)NC(CCCCN)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(C)C(=O)NC(CCC(=O)N)C(=O)NC(CC(C)C)C(=O)NC(CO)C(=O)NC(C)C(=O)NC(CCCNC(=N)N)C(=O)NC(CCCCN)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(CCC(=O)N)C(=O)NC(CC(=O)O)C(=O)NC(C(C)CC)C(=O)NC(CC(C)C)C(=O)NC(CO)C(=O)NC(CCCNC(=N)N)C(=O)N)NC(=O)C(C)NC(=O)C(CC(=O)O)NC(=O)C(C)NC(=O)C(CC3=CC=C(C=C3)O)N |
Every batch of CJC-1295 (No DAC) – 2mg is tested for purity and identity using industry-standard methods.
High-Performance Liquid Chromatography confirms purity ≥99%. Each batch is analyzed to ensure consistent quality.
Identity verification via mass spectrometry confirms correct molecular weight of 4113.58 g/mol.
All compounds undergo independent third-party laboratory testing for quality assurance.
Certificate of Analysis documents are available for all compounds. Contact us with your order number to request batch-specific documentation.
Each compound batch is tested by independent laboratories to verify purity, identity, and quality. The Certificate of Analysis (COA) provides transparent lab results, ensuring the compound meets strict research-grade standards.
Store at -20°C.
Protect from light and moisture.
| Test | Method | Result | Specification | |
|---|---|---|---|---|
| Identity | HPLC-DAD | CJC-1295 (No DAC) | CJC-1295 (No DAC) | Pass |
| Purity | HPLC-DAD | 99.64 | >99% by HPLC | Pass |
| Quantity | HPLC Analyte Concentration Curve Assay | 2.05 | 2mg | Pass |
| Endotoxins | LAL ELISA | 0.125 EU/mL | ≤ 0.5 EU/mL | Pass |
| Sterility | Pour Plate | No Growth | No Growth | Pass |
Learn more about CJC-1295
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Compounds are supplied for laboratory research use only and are not for human or veterinary use.