Melittin, CAS No.37231-28-0

CAS: 37231-28-0 Cat. No.: M329573 Formule: C131H229N39O31•x(C2HF3O2) Poids moléculaire: 2846.46 + x(114.02) Numéro CE: 253-417-7 PubChem CID: 16129627
DISPONIBLE À COMMANDE
GRADE & PURITY ≥97%
★
Size
Allemagne (EU)
USA*
Price
Qty
1mg
M329573-1mg
—
2 En stock

128,34€

173,46€
Enregistrer 45,12 € (26.01%)
5mg
M329573-5mg
—
3 En stock
350,48€
10mg
M329573-10mg
—
2 En stock
636,83€
25mg
M329573-25mg
—
2 En stock

1 103,68€

1 432,55€
Enregistrer 328,87 € (22.96%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Melittin, an antibacterial originally derived from|Apis mellifera|, has been reported to cause apoptosis via induction of reactive oxygen species production in cells. Additionally, this compound has been found to suppress 4α-Phorbol 12-myristate 13-acetate induced invasion of proliferative cells via inhibition of activator protein-1 and NF-κB. Other experiments show Melittin to be able to also suppress PMA-induced phosphorylation of ERK and JNK mitogen-activated protein kinases. This compound also activates phospholipase A2 (PLA2).

Specifications

Product Name
Melittin, CAS No.37231-28-0
Synonymes
Melittin | Q424512 | DTXSID40893812 | L-Glutamamide, glycyl-L-isoleucylglycyl-L-alanyl-L-valyl-L-leucyl-L-lysyl-L-valyl-L-leucyl-L-threonyl-L-threonylglycyl-L-leucyl-L-prolyl-L-alanyl-L-Leucyl-L-isoleucyl-L-seryl-L-tryptophyl-L-isoleucyl-L-lysyl-L-arginyl
Spécifications et pureté
≥97%
Séquence
Gly-Ile-Gly-Ala-Val-Leu-Lys-Val-Leu-Thr-Thr-Gly-Leu-Pro-Ala-Leu-Ile-Ser-Trp-Ile-Lys-Arg-Lys-Arg-Gln-Gln-NH2
Source
Synthetic
CAS
37231-28-0
Type de molécule
Peptide
Stockage et expédition
Conditions de stockage de stockage
Store at -20°C,Argon charged
Expédié en
Ice chest + Ice pads

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic Polymers
ClassePolypeptides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPolypeptides
Alternative Parents Peptides  Arginine and derivatives  Glutamine and derivatives  Isoleucine and derivatives  Leucine and derivatives  Valine and derivatives  Proline and derivatives  N-acyl-alpha amino acids and derivatives  Tryptamines and derivatives  Serine and derivatives  Alpha amino acid amides  Alanine and derivatives  3-alkylindoles  Pyrrolidinecarboxamides  N-acylpyrrolidines  N-acyl amines  Substituted pyrroles  Benzenoids  Heteroaromatic compounds  Tertiary carboxylic acid amides  Secondary carboxylic acid amides  Primary carboxylic acid amides  Secondary alcohols  Guanidines  Azacyclic compounds  Carboximidamides  Hydrocarbon derivatives  Monoalkylamines  Imines  Primary alcohols  Carbonyl compounds  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Polypeptide - Alpha peptide - Arginine or derivatives - Glutamine or derivatives - Isoleucine or derivatives - Leucine or derivatives - N-acyl-alpha amino acid or derivatives - Valine or derivatives - Proline or derivatives - Alpha-amino acid amide - Serine or derivatives - Triptan - Alanine or derivatives - Alpha-amino acid or derivatives - 3-alkylindole - N-substituted-alpha-amino acid - Indole - Indole or derivatives - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Substituted pyrrole - Benzenoid - Fatty amide - N-acyl-amine - Fatty acyl - Tertiary carboxylic acid amide - Pyrrolidine - Heteroaromatic compound - Pyrrole - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Secondary alcohol - Guanidine - Primary carboxylic acid amide - Azacycle - Carboximidamide - Organoheterocyclic compound - Carboxylic acid derivative - Primary amine - Hydrocarbon derivative - Imine - Amine - Organic oxide - Organic oxygen compound - Primary aliphatic amine - Carbonyl group - Alcohol - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Primary alcohol - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues.
External Descriptors Peptides
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot NumberCertificate TypeDateArticle
G2628112Certificate of AnalysisAug 04, 2026 M329573
I2202758Certificate of AnalysisJun 11, 2026 M329573
I2202759Certificate of AnalysisJun 11, 2026 M329573
I2202760Certificate of AnalysisJun 11, 2026 M329573
I2202761Certificate of AnalysisJun 11, 2026 M329573
D2614085Certificate of AnalysisApr 18, 2026 M329573
F2527100Certificate of AnalysisApr 02, 2026 M329573
G2502190Certificate of AnalysisApr 02, 2026 M329573
FAQ et articles
Citations of This Product
Références
1. Weibin Zhang, Zhe An, Yuqi Bai, Ying Zhou, Fangyi Chen, Ke-Jian Wang.  (2023)  A novel antimicrobial peptide Scyreptin1-30 from Scylla paramamosain exhibiting potential therapy of Pseudomonas aeruginosa early infection in a mouse burn wound model.  BIOCHEMICAL PHARMACOLOGY,      [PMID:37952897] [10.1016/j.bcp.2023.115917]
2. Fenfang Liu, Fen Chen, Le Yang, Fucheng Qiu, Guangen Zhong, Shan Gao, Weizhe Xi, Meilian Lai, Qiting He, Ying Chen, Weiming Chen, Jiping Zhang, Lu Yang.  (2023)  Melittin acupoint injection in attenuating bone erosion in collagen-induced arthritis mice via inhibition of the RANKL/NF-κB signaling pathway.  Quantitative Imaging in Medicine and Surgery,      [PMID:37711782] [10.21037/qims-23-254]
3. Li Li, Sufang Zhang, Lei Wei, Zhongfu Wang, Wei Ma, Fangying Liu, Yanhua Shen, Shanfang Zhang, Xiulian Zhang, Yu Hang, Yechang Qian.  (2020)  Anti-fibrotic effect of melittin on TRIM47 expression in human embryonic lung fibroblast through regulating TRIM47 pathway.  LIFE SCIENCES,      [PMID:32502539] [10.1016/j.lfs.2020.117893]
4. Liu Lei, Liu Jie, Cui Qi, Jia Bo-Yan, Pei Zhi-Hua, Odah Kokou Ayefounin, Wang Yi-Ming, Dong Wen-Long, Kong Ling-Cong, Ma Hong-Xia.  (2019)  Design and Characterization of a Novel Hybrid Antimicrobial Peptide OM19R Based on Oncocin and MDAP-2.  International Journal of Peptide Research and Therapeutics,  26  (4): (1839-1846).  [PMID:] [10.1007/s10989-019-09984-3]
5. Chenyue Qiu, Jinfa Ye, Lang Ke, Xingyuan Wei, Peiyu Wang, Yun Han, Xiaofei Wen, Gang Liu, Chengchao Chu.  (2025)  Virus-mimetic nanovesicle for the Hijacking- Integration-Vesicular amplification-Exocytosis treatment of ocular tumor.  Materials Today Advances,      [PMID:] [10.1016/j.mtadv.2025.100643]
6. Yinhui Qin, Na Zhang, Yan Yang, Yuetai Teng, Yinhu Wang, Weihong Niu.  (2025)  Development of marine-derived indole derivatives as novel antibacterial agents against gram-positive bacteria.  BIOORGANIC CHEMISTRY,      [PMID:41319447] [10.1016/j.bioorg.2025.109300]
7. Yihong Gao, Yinjia Luo, Zeting Wang, Shuhua Wei, Chunfu Wei, Xi Kong, Xiao Yue, Guanlin Wang, Chuanbin Wu, Ziyu Zhao, Wenhao Wang, Xuejuan Zhang.  (2026)  Nanodisrupter loaded nasal spray for membrane perturbation-assisted treatment of lung cancer brain metastases: A proof-of-concept in vitro study.  JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.jddst.2026.108279]
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