EcoDrugPlus


Keyword(s):	Surfactants
Molecule Category	Free-form

Keyword(s):

Surfactants

Molecule Category

Free-form


InChI Key	SKLCSKDLFFLXAG-UHFFFAOYSA-N
Smiles	NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCCCCCCCCCCCCCCCCC
InChI	InChI=1S/C44H91NO13/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-46-21-23-48-25-27-50-29-31-52-33-35-54-37-39-56-41-43-58-44-42-57-40-38-55-36-34-53-32-30-51-28-26-49-24-22-47-20-18-45/h2-45H2,1H3

InChI Key

SKLCSKDLFFLXAG-UHFFFAOYSA-N

Smiles

NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCCCCCCCCCCCCCCCCC

InChI

InChI=1S/C44H91NO13/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-46-21-23-48-25-27-50-29-31-52-33-35-54-37-39-56-41-43-58-44-42-57-40-38-55-36-34-53-32-30-51-28-26-49-24-22-47-20-18-45/h2-45H2,1H3

Property Name	Value
Molecular Formula	C44H91NO13
Molecular Weight	841.65
AlogP	6.42
Hydrogen Bond Acceptor	14.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	55.0
Polar Surface Area	146.01
Heavy Atoms	58.0

Property Name

Value

Molecular Formula

C44H91NO13

Molecular Weight

841.65

AlogP

6.42

Hydrogen Bond Acceptor

14.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

55.0

Polar Surface Area

146.01

Heavy Atoms

58.0

Resources	Reference
NORMAN SUSDAT

Resources

Reference

NORMAN SUSDAT


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).

AMINES, C18 SATURATED 13 EO

Structure

Physicochemical Descriptors

Cross References