MedKoo Cat#: 555807 | Name: SSAA09E1
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Description:

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

SSAA09E1 is an inhibitor of SARS-CoV replication that block viral entry by three different mechanisms.

Chemical Structure

SSAA09E1
CAS#433212-75-0

Theoretical Analysis

MedKoo Cat#: 555807

Name: SSAA09E1

CAS#: 433212-75-0

Chemical Formula: C7H9N3S2

Exact Mass: 199.0238

Molecular Weight: 199.29

Elemental Analysis: C, 42.19; H, 4.55; N, 21.09; S, 32.17

Price and Availability

Size Price Availability Quantity
5mg USD 265.00 2 Weeks
10mg USD 450.00 2 Weeks
25mg USD 750.00 2 Weeks
50mg USD 1,250.00 2 Weeks
100mg USD 1,650.00 2 Weeks
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Related CAS #
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Synonym
SSAA09E1; SSAA09 E1; SSAA09-E1;
IUPAC/Chemical Name
[(Z)-1-Thiophen-2-ylethylideneamino]thiourea
InChi Key
PJVHAJJEMJNPHN-UITAMQMPSA-N
InChi Code
InChI=1S/C7H9N3S2/c1-5(9-10-7(8)11)6-3-2-4-12-6/h2-4H,1H3,(H3,8,10,11)/b9-5-
SMILES Code
S=C(N)N/N=C(C1=CC=CS1)/C
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
To be determined
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:
SSAA09E1 reduces infection of HEK293T cells transiently transfected with angiotensin-converting enzyme 2 (ACE2) by an HIV-based virus system pseudotyped with SARS-CoV spike glycoprotein (EC50 = 6.7 μM). SSAA09E1 also inhibits the proteolytic activity of cathepsin L (IC50 = 5.33 µM) but not cathepsin B when used at a concentration of 20 µM.
In vitro activity:
SSAA09E1 blocked the activity of the host protease cathepsin L, which is necessary for the processing of the SARS-CoV surface glycoprotein during viral entry. This inhibition occurs at a later stage in the viral entry process. Reference: J Virol. 2013 Jul;87(14):8017-28. https://pubmed.ncbi.nlm.nih.gov/23678171/
In vivo activity:
To be determined

Preparing Stock Solutions

The following data is based on the product molecular weight 199.29 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. Adedeji AO, Severson W, Jonsson C, Singh K, Weiss SR, Sarafianos SG. Novel inhibitors of severe acute respiratory syndrome coronavirus entry that act by three distinct mechanisms. J Virol. 2013 Jul;87(14):8017-28. doi: 10.1128/JVI.00998-13. Epub 2013 May 15. PMID: 23678171; PMCID: PMC3700180.
In vitro protocol:
1. Adedeji AO, Severson W, Jonsson C, Singh K, Weiss SR, Sarafianos SG. Novel inhibitors of severe acute respiratory syndrome coronavirus entry that act by three distinct mechanisms. J Virol. 2013 Jul;87(14):8017-28. doi: 10.1128/JVI.00998-13. Epub 2013 May 15. PMID: 23678171; PMCID: PMC3700180.
In vivo protocol:
To be determined
Adedeji AO, Severson W, Jonsson C, Singh K, Weiss SR, Sarafianos SG. Novel inhibitors of severe acute respiratory syndrome coronavirus entry that act by three distinct mechanisms. J Virol. 2013 Jul;87(14):8017-28. doi: 10.1128/JVI.00998-13. Epub 2013 May 15. PMID: 23678171; PMCID: PMC3700180.