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SDMA - 10mM in DMSO, high purity , CAS No.30344-00-4

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SDMA - 10mM in DMSO, high purity , CAS No.30344-00-4

1 Citations

COA

Grade & Purity:

Moligand™

10mM in DMSO

Cas Number: 30344-00-4
Molecular Weight: 202.25
PubChem CID: 169148

In stock

Item Number

S423136

Grouped product items
SKU	Size	Availability	Price	Qty
S423136-1ml	1ml	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$241.90

View related series

Compound libraries (12325) Metabolite (5307)

Basic Description

Synonyms	SDMA \| 30344-00-4 \| symmetric dimethylarginine \| N,N'-Dimethylarginine \| (2S)-2-amino-5-[(N,N'-dimethylcarbamimidoyl)amino]pentanoic acid \| N(G1),N(G2)-Dimethylarginine \| (S)-2-Amino-5-((bis(methylamino)methylene)amino)pentanoic acid \| N3, N4-Dimethylarginine \| Guanidino
Specifications & Purity	Moligand™, 10mM in DMSO
Biochemical and Physiological Mechanisms	SDMA (Symmetric dimethylamine) is an endogenous inhibitor of nitric oxide (NO) synthase activity.
Storage Temp	Store at -80°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Grade	Moligand™
Product Description	Information SMDA (symmetric dimethylarginine) is a methylated form of arginine found within all nucleated cells that is released into circulation after proteolysis, then excreted through the kidneys, and correlates well with GFR (glomerular filtration rate) in people, dogs, and cats.

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 Arginine and derivatives

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
Direct Parent	Arginine and derivatives
Alternative Parents	L-alpha-amino acids Fatty acids and conjugates Guanidines Amino acids Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboxylic acids Carboximidamides Organopnictogen compounds Organic oxides Monoalkylamines Imines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Arginine or derivatives - Alpha-amino acid - L-alpha-amino acid - Fatty acid - Guanidine - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Amine - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Imine - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as arginine and derivatives. These are compounds containing arginine or a derivative thereof resulting from reaction of arginine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors	guanidines - non-proteinogenic L-alpha-amino acid - L-arginine derivative - dimethylarginine
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

ALogP	-3.419
hba_count	2
HBD Count	3
Rotatable Bond	7

Names and Identifiers

IUPAC Name	(2S)-2-amino-5-[(N,N'-dimethylcarbamimidoyl)amino]pentanoic acid
INCHI	InChI=1S/C8H18N4O2/c1-10-8(11-2)12-5-3-4-6(9)7(13)14/h6H,3-5,9H2,1-2H3,(H,13,14)(H2,10,11,12)/t6-/m0/s1
InChIKey	HVPFXCBJHIIJGS-LURJTMIESA-N
Smiles	CNC(=NC)NCCCC(C(=O)O)N
Isomeric SMILES	CNC(=NC)NCCC[C@@H](C(=O)O)N
Molecular Weight	202.25
Reaxy-Rn	4134786
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4134786&ln=

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

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility	40
DMSO(mM) Max Solubility	197.775030902349
Water(mg / mL) Max Solubility	40
Water(mM) Max Solubility	197.775030902349
Molecular Weight	202.250 g/mol
XLogP3	-3.700
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	7
Exact Mass	202.143 Da
Monoisotopic Mass	202.143 Da
Topological Polar Surface Area	99.700 Å²
Heavy Atom Count	14
Formal Charge	0
Complexity	206.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. SunHongzheng , HanLongsen , GuoYueshuai , AnHuiqing , WangBing , ZhangXiangzheng , LiJiashuo , JiangYingtong , WangYue , SunGuangyi , ZhuShuai , TangShoubin , GeJuan , ChenMinjian , GuoXuejiang , WangQiang. (2024) The global phosphorylation landscape of mouse oocytes during meiotic maturation. EMBO JOURNAL,

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