MedKoo Cat#: 574723 | Name: GKL-003
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Description:

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

GKL-003 is an inhibitor of Bacterial Transcription Initiation Complex formation.

Chemical Structure

GKL-003
GKL-003
CAS#1445801-61-5

Theoretical Analysis

MedKoo Cat#: 574723

Name: GKL-003

CAS#: 1445801-61-5

Chemical Formula: C34H28Cl2N4O6

Exact Mass: 658.1386

Molecular Weight: 659.52

Elemental Analysis: C, 61.92; H, 4.28; Cl, 10.75; N, 8.50; O, 14.56

Price and Availability

Size Price Availability Quantity
5mg USD 350.00 2 Weeks
10mg USD 650.00 2 Weeks
25mg USD 1,250.00 2 Weeks
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Related CAS #
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Synonym
GKL003; GKL-003; GKL 003
IUPAC/Chemical Name
3-(4-Chlorophenyl)-N'-(3-(4-chlorophenyl)-4,6-dimethoxy-1H-indole-7-carbonyl)-4,6-dimethoxy-1H-indole-7-carbohydrazide
InChi Key
VBILODCXAJTPGG-UHFFFAOYSA-N
InChi Code
InChI=1S/C34H28Cl2N4O6/c1-43-23-13-25(45-3)29(31-27(23)21(15-37-31)17-5-9-19(35)10-6-17)33(41)39-40-34(42)30-26(46-4)14-24(44-2)28-22(16-38-32(28)30)18-7-11-20(36)12-8-18/h5-16,37-38H,1-4H3,(H,39,41)(H,40,42)
SMILES Code
O=C(C1=C(OC)C=C(OC)C2=C1NC=C2C3=CC=C(Cl)C=C3)NNC(C4=C(OC)C=C(OC)C5=C4NC=C5C6=CC=C(Cl)C=C6)=O
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
>3 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
Product Data
Biological target:
GKL-003 is an inhibitor of Bacterial Transcription Initiation Complex formation.
In vitro activity:
This study has identified the region of RNAP to which these compounds bind and demonstrate that one compound, GKL003, has an inhibition constant in the low nanomolar range. This compound has activity against both Gram-positive and -negative organisms, including a community acquired methicillin-resistant strain of the major pathogen Staphylococcus aureus. Reference: ACS Chem Biol. 2013 Sep 20;8(9):1972-80. https://pubmed.ncbi.nlm.nih.gov/23751807/
In vivo activity:
TBD

Preparing Stock Solutions

The following data is based on the product molecular weight 659.52 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:
1. Ma C, Yang X, Kandemir H, Mielczarek M, Johnston EB, Griffith R, Kumar N, Lewis PJ. Inhibitors of bacterial transcription initiation complex formation. ACS Chem Biol. 2013 Sep 20;8(9):1972-80. doi: 10.1021/cb400231p. Epub 2013 Jul 5. PMID: 23751807.
In vitro protocol:
1. Ma C, Yang X, Kandemir H, Mielczarek M, Johnston EB, Griffith R, Kumar N, Lewis PJ. Inhibitors of bacterial transcription initiation complex formation. ACS Chem Biol. 2013 Sep 20;8(9):1972-80. doi: 10.1021/cb400231p. Epub 2013 Jul 5. PMID: 23751807.
In vivo protocol:
TBD
1. Ma C, Yang X, Kandemir H, et al. Inhibitors of bacterial transcription initiation complex formation. ACS Chem Biol. 2013;8(9):1972-1980. doi:10.1021/cb400231p