OpenMolDB

albendazole

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
265.33	5	2	3.32				JN_202	None		Not checked

SMILES: CCCSc1ccc2nc(NC(=O)OC)[nH]c2c1

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[albendazole]	4.26					Natalie J. Medlicott 2005
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[albendazole]	2.31				differential scanning calorimetry	Natalie J. Medlicott 2005

alizarin yellow-modified b-cyclodextrin

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					VD-0107	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[alizarin yellow-modified b-cyclodextrin](1).[ursodeoxycholic acid ]	4.97		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[chenodeoxycholic acid ]	3.96		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[deoxycholic acid ]	3.13		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[1-adamantanecarboxylic acid]	3.97		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[1-adamantanol]	3.91		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[d-camphor]	2.66		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[l-camphor]	2.59		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[d-menthol ]	2.96		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[l-menthol ]	3.00		9.4	25.0	Absorption and induced circular dichroism spectroscopy	Tetsuo Kuwabara 1998

alkannin/shikonin enantiomers

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_28(izoméria)	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[alkannin/shikonin enantiomers]	2.42		6.7	25.0	spectrophotometry	Hui-Wen Cheng 1996
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[alkannin/shikonin enantiomers]	1.19		9.0		HPLC	Hui-Wen Cheng 1996

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_474	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[a-Cyclodextrin](1).[alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form]	3.80		4.6	25.0	Uv-vis absorption spectroscopy, circular dichroism	Noboru Yoshida 1990
[b-Cyclodextrin](1).[alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form]	3.30		4.6	25.0	Uv-vis absorption spectroscopy, circular dichroism	Noboru Yoshida 1990

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_475	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_476	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_477	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_478	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_479	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_480	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_481	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_482	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_483	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_484	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_485	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref