BRD6688
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 562510

CAS#: 1404562-17-9

Description: BRD6688 is a selective HDAC2 inhibitor. It acts by enhancing the learning and memory processes.


Chemical Structure

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BRD6688
CAS# 1404562-17-9

Theoretical Analysis

MedKoo Cat#: 562510
Name: BRD6688
CAS#: 1404562-17-9
Chemical Formula: C16H18N4O
Exact Mass: 282.15
Molecular Weight: 282.340
Elemental Analysis: C, 68.06; H, 6.43; N, 19.84; O, 5.67

Price and Availability

Size Price Availability Quantity
1mg USD 190
5mg USD 430
10mg USD 760
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Synonym: BRD6688; BRD-6688; BRD 6688;

IUPAC/Chemical Name: N-[2-Amino-5-(4-pyridinyl)phenyl]-1-pyrrolidinecarboxamide

InChi Key: YZXBMJVMSBSGMM-UHFFFAOYSA-N

InChi Code: InChI=1S/C16H18N4O/c17-14-4-3-13(12-5-7-18-8-6-12)11-15(14)19-16(21)20-9-1-2-10-20/h3-8,11H,1-2,9-10,17H2,(H,19,21)

SMILES Code: O=C(N1CCCC1)NC2=CC(C3=CC=NC=C3)=CC=C2N

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 282.34 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Wagner FF, Zhang YL, Fass DM, Joseph N, Gale JP, Weïwer M, McCarren P, Fisher SL, Kaya T, Zhao WN, Reis SA, Hennig KM, Thomas M, Lemercier BC, Lewis MC, Guan JS, Moyer MP, Scolnick E, Haggarty SJ, Tsai LH, Holson EB. Kinetically Selective Inhibitors of Histone Deacetylase 2 (HDAC2) as Cognition Enhancers. Chem Sci. 2015 Jan 1;6(1):804-815. PubMed PMID: 25642316; PubMed Central PMCID: PMC4310013.