M760-2750 Screening compound: N-{1-[1-(4-methoxyphenyl)cyclopropanecarbonyl]azetidin-3-yl}-N-[(pyridin-2-yl)methyl]methanesulfonamide

M760-2750 Screening compound: N-{1-[1-(4-methoxyphenyl)cyclopropanecarbonyl]azetidin-3-yl}-N-[(pyridin-2-yl)methyl]methanesulfonamide
M760-2750 Screening compound: N-{1-[1-(4-methoxyphenyl)cyclopropanecarbonyl]azetidin-3-yl}-N-[(pyridin-2-yl)methyl]methanesulfonamide alternative view

Chemical Structure Depiction of ChemDiv screening compound M760-2750
N-{1-[1-(4-methoxyphenyl)cyclopropanecarbonyl]azetidin-3-yl}-N-[(pyridin-2-yl)methyl]methanesulfonamide

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

M760-2750

Molecular Formula

C21H25N3O4S (C21 H25 N3 O4 S)

Compound Name

N-{1-[1-(4-methoxyphenyl)cyclopropanecarbonyl]azetidin-3-yl}-N-[(pyridin-2-yl)methyl]methanesulfonamide

IUPAC name

N-{1-[1-(4-methoxyphenyl)cyclopropanecarbonyl]azetidin-3-yl}-N-[(pyridin-2-yl)methyl]methanesulfonamide

SMILES

COc1ccc(C2(CC2)C(N(C2)CC2N(Cc2ncccc2)S(C)(=O)=O)=O)cc1

MDL Number (MFCD)

Chemical and Physical Properties

Saltdata

n/a

Molecular Weight

415.51

Hydrogen Bond Acceptors Count

9.00

Hydrogen Bond Donors Count

0.00

Rotatable Bond Count

8.00

Number of Nitrogen and Oxygen Atoms

7

Partition Coefficient, logP

1.435

Distribution Coefficient, logD

1.182

Water Solubility, LogSw

-2.23

Polar Surface Area

65.382

Acid Dissociation Constant (pKa)

21.04

Base Dissociation Constant (pKb)

7.30

Number of Chiral Centers

0.00

Percent sp3 carbon bonding

42.86

M760-2750 in Drug Discovery

Included in Screening Libraries

3D-Pharmacophore Based Diversity Library (49813 compounds)

300k Representative Compounds Library (Bemis-Murcko Clustering Algorithm) (286253 compounds)

Protein-Protein Interaction Library (218420 compounds)

Anti-HIV1 Library (19540 compounds)

Beyond the Flatland Library sp3 enriched (92988 compounds)

Type II Kinase Inhibitors Library (6956 compounds)

Included in 1.7M Stock Database

Mechanism of action:
  • PPI modulators
Therapeutical areas:
  • Antiviral
  • Infections
  • Immune system
  • Digestive system
  • Hemic and lymphatic
  • Endocrine
Structure:
  • Cyclic compounds
Targets:
  • Kinases

References: we are preparing a list of scientific research reports with M760-2750 chemical compound. It will be published here after verification.

Frequently Asked Questions

How to purchase chemical compound M760-2750?
Check Price and Availability of M760-2750, 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 M760-2750 you sell to drug discovery company or institution?
Available from 1 mg in Glass Vials or 96-tube racks.
Delivery options for M760-2750
ChemDiv sends parcels with Express services (UPS, WC).
  • 1–2 days for small orders
  • 2–4 weeks for large selections
Delivery formats for M760-2750
  • 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 M760-2750 available by request