D269-0102 Screening compound: 3-chloro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide

D269-0102 Screening compound: 3-chloro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide
D269-0102 Screening compound: 3-chloro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide alternative view

Chemical Structure Depiction of ChemDiv screening compound D269-0102
3-chloro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide

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

D269-0102

Molecular Formula

C15H10ClN3OS (C15 H10 ClN3 OS)

Compound Name

3-chloro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide

IUPAC name

3-chloro-N-(3-phenyl-124-thiadiazol-5-yl)benzamide

SMILES

O=C(c1cccc(Cl)c1)Nc1nc(-c2ccccc2)ns1

InChI

InChI=1S/C15H10ClN3OS/c16-12-8-4-7-11(9-12)14(20)18-15-17-13(19-21-15)10-5-2-1-3-6-10/h1-9H,(H,17,18,19,20)

InChI Key

XTAPQZFLISAXMB-UHFFFAOYSA-N

MDL Number (MFCD)

MFCD12915867

Chemical and Physical Properties

Saltdata

n/a

Molecular Weight

315.78

Hydrogen Bond Acceptors Count

4.00

Hydrogen Bond Donors Count

1.00

Rotatable Bond Count

4.00

Number of Nitrogen and Oxygen Atoms

4

Partition Coefficient, logP

4.589

Distribution Coefficient, logD

4.549

Water Solubility, LogSw

-4.78

Polar Surface Area

43.917

Acid Dissociation Constant (pKa)

8.41

Base Dissociation Constant (pKb)

-4.35

Number of Chiral Centers

0.00

Percent sp3 carbon bonding

0.00

D269-0102 in Drug Discovery

Included in Screening Libraries

Allosteric Kinases Inhibitors Library (23117 compounds)

Anti-Aging Library (44940 compounds)

Adenosine Receptors Targeted Library (19896 compounds)

Included in 1.7M Stock Database

Therapeutical areas:
  • Cancer
  • Female
  • Congenital
  • Skin
  • Cancer
  • Musculoskeletal
  • Metabolic
  • Immune system
  • Cancer
  • Digestive system
  • Respiratory tract
  • Nervous system
  • Eye
  • Cardiovascular
Targets:
  • Kinases
  • GPCR
Mechanism of action:
  • Epigenetic
  • Receptor's ligands

References: we are preparing a list of scientific research reports with D269-0102 chemical compound. It will be published here after verification.

Frequently Asked Questions

How to purchase chemical compound D269-0102?
Check Price and Availability of D269-0102, 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 D269-0102 you sell to drug discovery company or institution?
Available from 1 mg in Glass Vials or 96-tube racks.
Delivery options for D269-0102
ChemDiv sends parcels with Express services (UPS, WC).
  • 1–2 days for small orders
  • 2–4 weeks for large selections
Delivery formats for D269-0102
  • 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 D269-0102 available by request