G210-2709 Screening compound: 2,7-dimethyl-3-phenyl-N-(4-phenylbutan-2-yl)pyrazolo[1,5-a]pyrimidine-6-carboxamide

G210-2709 Screening compound: 2,7-dimethyl-3-phenyl-N-(4-phenylbutan-2-yl)pyrazolo[1,5-a]pyrimidine-6-carboxamide
G210-2709 Screening compound: 2,7-dimethyl-3-phenyl-N-(4-phenylbutan-2-yl)pyrazolo[1,5-a]pyrimidine-6-carboxamide alternative view

Chemical Structure Depiction of ChemDiv screening compound G210-2709
2,7-dimethyl-3-phenyl-N-(4-phenylbutan-2-yl)pyrazolo[1,5-a]pyrimidine-6-carboxamide

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

G210-2709

Molecular Formula

C25H26N4O (C25 H26 N4 O)

Compound Name

2,7-dimethyl-3-phenyl-N-(4-phenylbutan-2-yl)pyrazolo[1,5-a]pyrimidine-6-carboxamide

IUPAC name

27-dimethyl-3-phenyl-N-(4-phenylbutan-2-yl)pyrazolo[15-a]pyrimidine-6-carboxamide

SMILES

CC(CCc1ccccc1)NC(c1c(C)n2nc(C)c(-c3ccccc3)c2nc1)=O

InChI

InChI=1S/C25H26N4O/c1-17(14-15-20-10-6-4-7-11-20)27-25(30)22-16-26-24-23(21-12-8-5-9-13-21)18(2)28-29(24)19(22)3/h4-13,16-17H,14-15H2,1-3H3,(H,27,30)/t17-/m0/s1

InChI Key

SXKOBSIDIIVKLU-KRWDZBQOSA-N

MDL Number (MFCD)

MFCD14986611

Chemical and Physical Properties

Saltdata

n/a

Molecular Weight

398.51

Hydrogen Bond Acceptors Count

4.00

Hydrogen Bond Donors Count

1.00

Rotatable Bond Count

7.00

Number of Nitrogen and Oxygen Atoms

5

Partition Coefficient, logP

4.060

Distribution Coefficient, logD

4.060

Water Solubility, LogSw

-4.31

Polar Surface Area

44.644

Acid Dissociation Constant (pKa)

13.38

Base Dissociation Constant (pKb)

3.02

Number of Chiral Centers

1.00

Percent sp3 carbon bonding

24.00

G210-2709 in Drug Discovery

Included in Screening Libraries

CNS Targets (44014 compounds)

Glucocorticoid receptors Library (4806 compounds)

Included in 1.7M Stock Database

Therapeutical areas:
  • Nervous system
  • Cancer
  • Nervous system
  • Hemic and lymphatic
  • Congenital
  • Metabolic
  • Endocrine
Targets:
  • Nuclear receptors
Mechanism of action:
  • Receptor's ligands

References: we are preparing a list of scientific research reports with G210-2709 chemical compound. It will be published here after verification.

Frequently Asked Questions

How to purchase chemical compound G210-2709?
Check Price and Availability of G210-2709, 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 G210-2709 you sell to drug discovery company or institution?
Available from 1 mg in Glass Vials or 96-tube racks.
Delivery options for G210-2709
ChemDiv sends parcels with Express services (UPS, WC).
  • 1–2 days for small orders
  • 2–4 weeks for large selections
Delivery formats for G210-2709
  • 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 G210-2709 available by request