OpenMolDB

Naphthalene

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
128.17	0	0	2.84				nt1949	None		Not checked

SMILES: c1ccc2ccccc2c1

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[g-Cyclodextrin](1).[Naphthalene]	2.11			25.0		Kenneth A. Connors 1995

Naphthalene-d8-β-cyclodextrin

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					VD-0086	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[Naphthalene-d8-β-cyclodextrin](1).[adamantane]	2.83		7.0	20.0	Absorption and fluorescence spectroscopy	V. B. Nazarov 2003

Naproxen

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
230.26	3	1	3.04				nt1558	None		Not checked

SMILES: COc1ccc2cc(ccc2c1)C(C)C(O)=O

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[b-Cyclodextrin](1).[Naproxen]	3.14			25.0		Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Naproxen]	3.98	1.95	2.0	15.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.76	1.95	2.0	25.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.58	2.46	2.0	35.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.40	2.41	2.0	45.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.89	1.90	3.0	15.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.71	2.80	3.0	25.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.53	2.41	3.0	35.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.36	2.08	3.0	45.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.74	2.43	4.0	15.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.57	2.76	4.0	25.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.39	1.70	4.0	35.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.23		4.0	45.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.48	1.48	5.0	15.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.19	1.60	5.0	25.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.06	2.00	5.0	35.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.00	1.95	5.0	45.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.32	1.85	6.0	15.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.17	1.85	6.0	25.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	3.05		6.0	35.0	Fluorescence spectroscopy	I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen]	2.87	1.30	6.0	45.0	Fluorescence spectroscopy	I. Vélaz 1997

Naproxen

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
230.26	3	1	3.04				VR_C106	None		Not checked

SMILES: COc1ccc2cc(ccc2c1)C(C)C(O)=O

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

Naproxen anion

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					nt1559	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[b-Cyclodextrin](1).[Naproxen anion]	1.43			25.0		Kenneth A. Connors 1995

Naproxen anion

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					nt1560	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

Naproxen anion

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					nt1561	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

Ni(II)-A-b-CD

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					VD-0090	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[Ni(II)-A-b-CD](1).[R-27-T3]	3.60					George W. Gokel 2003
[Ni(II)-A-b-CD](1).[S-27-T3]	4.40					George W. Gokel 2003

Ni2+

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					JN_398	None

SMILES: [Ni++]

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[6A-(3-Aminopropylamino)-6A-deoxy-BCD](1).[Ni2+]	5.20	0.10		25.0	pH titration	Stephen F. Lincoln 1994
[protonated form of 6A-(3-Aminopropylamino)-6A-deoxy-BCD](1).[Ni2+]	3.10	0.10		25.0	pH titration	Stephen F. Lincoln 1994

Nicotin

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
162.23	2	0	1.79				NT_a0015	None		Not checked

SMILES: CN1CCCC1c2cccnc2

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[b-Cyclodextrin](1).[Nicotin]	1.34	1.08		25.0	Capillary electrophoresis	Berglund, Johan 1997
[b-Cyclodextrin](1).[Nicotin]	1.34	1.08		37.0	Capillary electrophoresis	Berglund, Johan 1997
[b-Cyclodextrin](1).[Nicotin]	2.55		10.0		Capillary electrophoresis	Berglund, Johan 1997
[b-Cyclodextrin](1).[Nicotin]	2.38		10.0	25.0	Capillary electrophoresis	Berglund, Johan 1997

Nicotin

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
162.23	2	0	1.79				NT_a0016	None		Not checked

SMILES: CN1CCCC1c2cccnc2

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

Niflumic acid anion

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					nt1562	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[b-Cyclodextrin](1).[Niflumic acid anion]	2.72			25.0		Kenneth A. Connors 1995

Niflumic acid anion

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
	None	None					nt1563	None

SMILES:

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref

Nile Blue

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
353.85	3	1	2.43				JN_329	None		Not checked

SMILES: [Cl-].CCN(CC)c1ccc2nc3c(cc(N)c4ccccc34)[o+]c2c1

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[b-Cyclodextrin](1).[Nile Blue]	3.28		7.0	25.0	UV-vis spectroscopy	Hong-Yuan Chen 2002
[b-Cyclodextrin](1).[Nile Blue]	3.08		7.2	25.0	electrochemical characterization	Hong-Yuan Chen 2002

Nimetazepam

MW	HBA	HBD	LogP	CAS	Suppliers	Supplier IDs	Storage ID	Quantity	Class	PAINS
295.29	4	0	2.43				nt0625	None		Not checked

SMILES: CN1C(=O)CN=C(c2ccccc2)c3cc(ccc13)[N+]([O-])=O

Supramolecules

Name	log K	SD	pH	T(°C)	Method	Ref
[a-Cyclodextrin](1).[Nimetazepam]	1.38			25.0		Kenneth A. Connors 1995