ecallantide, INHIBITOR of Plasma kallikrein inhibitor, CAS No.460738-38-9, INHIBITOR of Plasma kallikrein inhibitor

CAS: 460738-38-9 Cat. No.: rp173941 PubChem CID: 44152182
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
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Size
Status
Price
Qty
500μg
rp173941-500μg
1-2 wks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$2,399.90
1mg
rp173941-1mg
1-2 wks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$3,999.90
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Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Product Name
ecallantide, INHIBITOR of Plasma kallikrein inhibitor, CAS No.460738-38-9
Synonyms
DX-88 | Kalbitor | GTPL6955 | FOV2302 | Ecallantide
Grade
Moligand™
Specifications & Purity
Moligand™
Action Type
INHIBITOR
Mechanism of action
INHIBITOR of Plasma kallikrein inhibitor
CAS
460738-38-9
Molecule Type
Peptide
Storage and Shipping
Storage
Room temperature

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.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic Polymers
ClassPolypeptides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPolypeptides
Alternative Parents Cyclic peptides  Arginine and derivatives  Phenylalanine and derivatives  Histidine and derivatives  Glutamic acid and derivatives  Aspartic acid and derivatives  Methionine and derivatives  N-acyl-L-alpha-amino acids  Acyl L-homoserines  Serine and derivatives  Alpha amino acid amides  Alanine and derivatives  Amphetamines and derivatives  3-alkylindoles  Amino fatty acids  1-hydroxy-2-unsubstituted benzenoids  Hydroxy fatty acids  Substituted pyrroles  N-acyl amines  Pyrrolidines  Tertiary carboxylic acid amides  Heteroaromatic compounds  Imidazoles  Guanidines  Primary carboxylic acid amides  Secondary carboxylic acid amides  Amino acids  Secondary alcohols  Organic disulfides  Lactams  Dialkylthioethers  Carboxylic acids  Carboximidamides  Azacyclic compounds  Sulfenyl compounds  Carbonyl compounds  Hydrocarbon derivatives  Imines  Monoalkylamines  Organic oxides  Primary alcohols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Polypeptide - Cyclic alpha peptide - Arginine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Glutamic acid or derivatives - Aspartic acid or derivatives - Methionine or derivatives - Acyl-homoserine - Acyl-l-homoserine - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-l-alpha-amino acid - Serine or derivatives - Alpha-amino acid amide - Alanine or derivatives - Amphetamine or derivatives - 3-alkylindole - Alpha-amino acid or derivatives - N-substituted-alpha-amino acid - Indole or derivatives - Indole - Amino fatty acid - 1-hydroxy-2-unsubstituted benzenoid - Hydroxy fatty acid - Phenol - Fatty acyl - N-acyl-amine - Monocyclic benzene moiety - Benzenoid - Substituted pyrrole - Fatty amide - Heteroaromatic compound - Azole - Pyrrole - Tertiary carboxylic acid amide - Imidazole - Pyrrolidine - Amino acid or derivatives - Amino acid - Carboxamide group - Guanidine - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Primary carboxylic acid amide - Organic disulfide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Thioether - Carboximidamide - Carboxylic acid - Sulfenyl compound - Dialkylthioether - Organosulfur compound - Organic oxide - Imine - Organic oxygen compound - Carbonyl group - Amine - Alcohol - Organic nitrogen compound - Primary aliphatic amine - Hydrocarbon derivative - Primary amine - Primary alcohol - Organonitrogen compound - Organooxygen compound - 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 Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Genetic information
Alternate NamesDX-88 | Kalbitor | GTPL6955 | FOV2302 | Ecallantide
Reference
  • 1. Kinetics and inhibition of recombinant human cystathionine gamma-lyase. Toward the rational control of transsulfuration., The Journal of biological chemistry, Steegborn, C C and 7 more authors.
  • 2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences., Proceedings of the National Academy of Sciences of the United States of America, Strausberg, Robert L RL and 83 more authors.
  • 3. Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)., Human genetics, Wang, Jian J and Hegele, Robert A RA.
  • 4. Cloning and nucleotide sequence of human liver cDNA encoding for cystathionine gamma-lyase., Biochemical and biophysical research communications, Lu, Y Y, O'Dowd, B F BF, Orrego, H H and Israel, Y Y.
  • 5. Single nucleotide polymorphism in CTH associated with variation in plasma homocysteine concentration., Clinical genetics, Wang, J J, Huff, A M AM, Spence, J D JD and Hegele, R A RA.
  • 6. Cystathionine gamma-lyase overexpression inhibits cell proliferation via a H2S-dependent modulation of ERK1/2 phosphorylation and p21Cip/WAK-1., The Journal of biological chemistry, Yang, Guangdong G, Cao, Kun K, Wu, Lingyun L and Wang, Rui R.
  • 7. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)., Genome research, Gerhard, Daniela S DS and 115 more authors.
  • 8. Towards a proteome-scale map of the human protein-protein interaction network., Nature, Rual, Jean-François JF and 37 more authors.
  • 9. The DNA sequence and biological annotation of human chromosome 1., Nature, Gregory, S G SG and 178 more authors.
  • 10. Polymorphisms in one-carbon metabolism and trans-sulfuration pathway genes and susceptibility to bladder cancer., International journal of cancer, Moore, Lee E LE and 14 more authors. more
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