D420-6138 Screening compound: N-cyclopentyl-4-[3-(2-hydroxy-7-methylquinolin-3-yl)-1,2,4-oxadiazol-5-yl]butanamide

D420-6138 Screening compound: N-cyclopentyl-4-[3-(2-hydroxy-7-methylquinolin-3-yl)-1,2,4-oxadiazol-5-yl]butanamide
D420-6138 Screening compound: N-cyclopentyl-4-[3-(2-hydroxy-7-methylquinolin-3-yl)-1,2,4-oxadiazol-5-yl]butanamide alternative view

Chemical Structure Depiction of ChemDiv screening compound D420-6138
N-cyclopentyl-4-[3-(2-hydroxy-7-methylquinolin-3-yl)-1,2,4-oxadiazol-5-yl]butanamide

Available from 1 mg

Formats:

  • Glass Vials (4ml Glass Vials VWR #97047-678)
  • 96-tube racks (Matrix #4247 96-well 1.4ml sealed with capmats, empty cols 1 & 12, 100uL of 10mM)

Shiptime: 1 week worldwide delivery in most cases

Compound Identifiers

ChemDiv Compound ID

D420-6138

Molecular Formula

C21H24N4O3 (C21 H24 N4 O3)

Compound Name

N-cyclopentyl-4-[3-(2-hydroxy-7-methylquinolin-3-yl)-1,2,4-oxadiazol-5-yl]butanamide

IUPAC name

N-cyclopentyl-4-[3-(2-hydroxy-7-methylquinolin-3-yl)-124-oxadiazol-5-yl]butanamide

SMILES

Cc1ccc(cc(-c2noc(CCCC(NC3CCCC3)=O)n2)c(O)n2)c2c1

InChI

InChI=1S/C21H24N4O3/c1-13-9-10-14-12-16(21(27)23-17(14)11-13)20-24-19(28-25-20)8-4-7-18(26)22-15-5-2-3-6-15/h9-12,15H,2-8H2,1H3,(H,22,26)(H,23,27)

InChI Key

YGJBRLMNWMLWJZ-UHFFFAOYSA-N

MDL Number (MFCD)

MFCD14828006

Chemical and Physical Properties

Saltdata

n/a

Molecular Weight

380.45

Hydrogen Bond Acceptors Count

7.00

Hydrogen Bond Donors Count

2.00

Rotatable Bond Count

7.00

Number of Nitrogen and Oxygen Atoms

7

Partition Coefficient, logP

3.555

Distribution Coefficient, logD

3.085

Water Solubility, LogSw

-3.80

Polar Surface Area

81.164

Acid Dissociation Constant (pKa)

7.11

Base Dissociation Constant (pKb)

2.46

Number of Chiral Centers

0.00

Percent sp3 carbon bonding

42.90

D420-6138 in Drug Discovery

Included in Screening Libraries

Targeted Diversity Library (40567 compounds)

Protein Tyrosine Phosphatase Non-receptor Type (PTPN) Targeted Library (32556 compounds)

Included in 1.7M Stock Database

Therapeutical areas:
  • Cancer
  • Nervous system
  • Male
  • Female
  • Hemic and lymphatic
  • Skin
  • Endocrine
Targets:
  • Phosphatases

References: we are preparing a list of scientific research reports with D420-6138 chemical compound. It will be published here after verification.

Frequently Asked Questions

How to purchase chemical compound D420-6138?
Check Price and Availability of D420-6138, then you can add required amount to the Shopping Cart. In the Shopping Cart you can again refine your selection. Once you are sure that it’s exactly what you want you can move forward with the Checkout (to pay online by credit card, or via PayPal), or Request a Quote.
What is the minimum amount of D420-6138 you sell to drug discovery company or institution?
Available from 1 mg in Glass Vials or 96-tube racks.
Delivery options for D420-6138
ChemDiv sends parcels with Express services (UPS, WC).
  • 1–2 days for small orders
  • 2–4 weeks for large selections
Delivery formats for D420-6138
  • 0.5–50 mg of dry powder sample in single glass vials, custom vials
  • DMSO solutions frozen 10μl–250μl@10mM (96 and 384 format)

Custom synthesis of D420-6138 available by request