Not Authenticated — sign in

Active cart: Temporary Cart (0 items)

Introduction

IUPHAR Database is the official database of the IUPHAR Committee on Receptor Nomenclature and Drug Classification. The paper is: Sharman JL, Benson HE, Pawson AJ, Lukito V, Mpamhanga CP, Bombail V, Davenport AP, Peters JA, Spedding M, Harmar AJ, and NC-IUPHAR. (2013) IUPHAR-DB: updated database content and new features. Nucl. Acids Res. 41 (Database Issue): D1083-8. We are grateful to the authors for curating and curating this resource, and thank them for allowing us to incorporate its structures in ZINC.

Contact Information

Website

http://www.iuphar-db.org

Email

Not available

Phone

no phone, not a vend

Fax

no fax, not a vendor

ZINC Subset Overview

Last updated

2013-02-24

Source catalog size

3,491

Number filtered out

250

Upload to PubChem?

No

Purchasability

Not for Sale (Annotated)

Quick Links

Browse

Sample molecules

Detailed view

Annotations

Files

Properties

Purchasing

Only from this vendor

Unix download

mol2 unix

SDF unix

Flexibase unix [Scripts to download database files on Linux and MacOS]

Win download

mol2 windows

SDF windows

Flexibase windows [Scripts to download database files on Windows]

Chemical Diversity and Clustering

We assess the chemical diversity of a subset by clustering the molecules. First, we sort ligands by increasing molecular weight. Then, we use the SUBSET 1.0 algorithm ( Voigt JH, Bienfait B, Wang S, Nicklaus MC. JCICS, 2001, 41, 702-12) to progressively select compounds that differ from those previously selected by at least the Tanimoto cutoff, using ChemAxon default fingerprints. The resulting representatives have two interesting properties:

• 1) Each representative differs from all the others by at least the Tanitmoto cutoff and
• 2) All the molecules in the subset are within the Tanimoto cutoff of at least one representative.

Thus the representatives can be said to "cover" the chemical space of the subset at a given Tanimoto level. N/A indicates that clustering is pending.

Tanimoto Cutoff Level	60%	70%	80%	90%	100%
Number of Representatives	823	1,075	1,280	1,514	2,344

Physical Property Distributions

We compute the physical properties of each molecule in the subset, and graph them below.   Download Calculated Physical Properties
 

Tab-delimited information files

• Calculated Physical Properties
• Source Catalog Information - Download strongly advised! This information changes rapidly.
• Substances only available from here (346) - correct when the subset was prepared.

Ready-to-dock molecular files

More about this.

Format	Reference(pH 7)	Mid(pH 6-8)	High(pH 8-9.5)	Low(pH 4.5-6)	Download Unix	Download Windows
SMILES	All	All	All	All
MOL2	All	All	All	All	Single Usual Metals All	Single Usual Metals All
SDF	All	All	All	All	Single Usual Metals All	Single Usual Metals All
Flexibase	0 1	All	All	All	Single Usual Metals All	Single Usual Metals All