EcoDrugPlus


Keyword(s):	Food Contact Chemicals
Molecule Category	Salt-form

Keyword(s):

Food Contact Chemicals

Molecule Category

Salt-form


InChI Key	BEBLEPZOMMWNIF-UHFFFAOYSA-L
Smiles	CC(C)(CS(=O)(=O)[O-])NC(=O)C=C.CC(C)(CS(=O)(=O)[O-])NC(=O)C=C.[Ca+2]
InChI	InChI=1S/2C7H13NO4S.Ca/c21-4-6(9)8-7(2,3)5-13(10,11)12;/h24H,1,5H2,2-3H3,(H,8,9)(H,10,11,12);/q;;+2/p-2

InChI Key

BEBLEPZOMMWNIF-UHFFFAOYSA-L

Smiles

CC(C)(CS(=O)(=O)[O-])NC(=O)C=C.CC(C)(CS(=O)(=O)[O-])NC(=O)C=C.[Ca+2]

InChI

InChI=1S/2C7H13NO4S.Ca/c2*1-4-6(9)8-7(2,3)5-13(10,11)12;/h2*4H,1,5H2,2-3H3,(H,8,9)(H,10,11,12);/q;;+2/p-2

Property Name	Value
Molecular Formula	C14H24CaN2O8S2
Molecular Weight	452.06
AlogP	-0.33
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	8.0
Polar Surface Area	179.58
Heavy Atoms	27.0

Property Name

Value

Molecular Formula

C14H24CaN2O8S2

Molecular Weight

452.06

AlogP

-0.33

Hydrogen Bond Acceptor

8.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

8.0

Polar Surface Area

179.58

Heavy Atoms

27.0

Resources	Reference
CAS NUMBER	95176-15-1
NORMAN SUSDAT
PubChem	72941626

Resources

Reference

CAS NUMBER

95176-15-1

NORMAN SUSDAT

PubChem

72941626


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

2-ACRYLAMIDO-2-METHYLPROPANESULFONIC ACID, CALCIUM SALT

Structure

Physicochemical Descriptors

Cross References