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Protein Tyrosine Kinase/RTK
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Bucillamine - 96%, high purity , Antioxidant, CAS No.65002-17-7, Antioxidant

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Bucillamine - 96%, high purity , Antioxidant, CAS No.65002-17-7, Antioxidant

COA

Grade & Purity:

≥96%

Cas Number: 65002-17-7
Molecular Weight: 223.31
PubChem CID: 656604
PubChem SID: 504759779

In stock

Item Number

B337598

Grouped product items
SKU	Size	Availability	Price
B337598-10mg	10mg	5	$38.90
B337598-50mg	50mg	4	$171.90
B337598-100mg	100mg	2	$228.90
B337598-250mg	250mg	2	$513.90
B337598-500mg	500mg	2	$923.90
B337598-1g	1g	2	$1,662.90

View related series

Receptor Tyrosine Kinase (1260)

Basic Description

Synonyms	Bucilant \| bucillamine \| N-(2-Mercaptoisobutyryl)-L-cysteine \| Thiobutarit \| BDBM50406934 \| CHEBI:31312 \| Q-101254 \| Bucilant (TN) \| (2R)-3-mercapto-2-[(2-mercapto-2-methyl-1-oxopropyl)amino]propanoic acid \| NCGC00182062-02 \| AKOS015895462 \| DE019; SA96;T
Specifications & Purity	≥96%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action	Antioxidant
Product Description	Bucillamine is an antirheumatic agent.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 N-acyl-alpha amino acids and derivatives
        Level8 N-acyl-alpha amino acids
        Level9 N-acyl-L-alpha-amino acids

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives - N-acyl-alpha amino acids and derivatives - N-acyl-alpha amino acids
Direct Parent	N-acyl-L-alpha-amino acids
Alternative Parents	Cysteine and derivatives Secondary carboxylic acid amides Monocarboxylic acids and derivatives Carboxylic acids Alkylthiols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	N-acyl-l-alpha-amino acid - Cysteine or derivatives - Carboxamide group - Secondary carboxylic acid amide - Alkylthiol - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Product Properties

pKa	pKa: 3.01 (Predicted)
ALogP	0.4

Associated Targets(Human)

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

Discover Target: ACE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504759779
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504759779
IUPAC Name	(2R)-2-[(2-methyl-2-sulfanylpropanoyl)amino]-3-sulfanylpropanoic acid
INCHI	InChI=1S/C7H13NO3S2/c1-7(2,13)6(11)8-4(3-12)5(9)10/h4,12-13H,3H2,1-2H3,(H,8,11)(H,9,10)/t4-/m0/s1
InChIKey	VUAFHZCUKUDDBC-BYPYZUCNSA-N
Smiles	CC(C)(C(=O)NC(CS)C(=O)O)S
Isomeric SMILES	CC(C)(C(=O)N[C@@H](CS)C(=O)O)S
RTECS	HA2420000
Molecular Weight	223.31
Reaxy-Rn	2643663
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2643663&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

12 results found

Lot Number	Certificate Type	Date	Item
G2312316	Certificate of Analysis	Jun 16, 2023	B337598
G2312315	Certificate of Analysis	Jun 16, 2023	B337598
G2312313	Certificate of Analysis	Jun 16, 2023	B337598
G2312311	Certificate of Analysis	Jun 16, 2023	B337598
G2312328	Certificate of Analysis	Jun 16, 2023	B337598
G2312310	Certificate of Analysis	Jun 16, 2023	B337598
G2312308	Certificate of Analysis	Jun 16, 2023	B337598
G2312302	Certificate of Analysis	Jun 16, 2023	B337598
G2312324	Certificate of Analysis	Jun 16, 2023	B337598
G2312322	Certificate of Analysis	Jun 16, 2023	B337598
G2312321	Certificate of Analysis	Jun 16, 2023	B337598
G2312319	Certificate of Analysis	Jun 16, 2023	B337598

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Chemical and Physical Properties

Solubility	Soluble in ethanol, and methanol.
Refractive Index	n20D1.55 (Predicted)
Boil Point(°C)	438° C (Predicted)
Melt Point(°C)	119-123° C
Molecular Weight	223.300 g/mol
XLogP3	0.400
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	4
Exact Mass	223.034 Da
Monoisotopic Mass	223.034 Da
Topological Polar Surface Area	68.400 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	218.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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