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BLT-1 - 98%, high purity , CAS No.321673-30-7

    Grade & Purity:
  • ≥98%
In stock
Item Number
B412587
Grouped product items
SKU Size
Availability
Price Qty
B412587-10mg
10mg
3
$128.90
B412587-25mg
25mg
3
$272.90
B412587-50mg
50mg
3
$463.90
B412587-100mg
100mg
2
$787.90
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Basic Description

Synonyms 33M20 | Probes2_000409 | DTXSID80430563 | Probes1_000008 | Probes1_000093 | Probes2_000390 | BLT-1 | E74752 | EN300-68381 | (2Z)-2-(2-hexylcyclopentylidene)hydrazinecarbothioamide | EX-A4880 | [(2-hexylcyclopentylidene)amino]thiourea | Z275117012 | SCHEMB
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms BLT-1 is an inhibitor of HDL receptor SR-BI. BLT-1 is primarily used for phosphorylation and dephosphorylation applications.Block lipid transport-1 (BLT-1) is a specific inhibitor of the SR-BI (Scavenger receptor, class B, type I) mediated lipid transfer.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

BLT-1 (Block lipid transport-1) has been used as an inhibitor of the SR-BI (scavenger receptor, class B, type I) mediated lipid transfer to determine if miR-223-3p export from polymorphonuclear neutrophils (PMNs) to high-density lipoproteins (HDLs) is dependent on SR-BI-mediated lipid flux. It has also been used as a SR-BI inhibitor to study the effect of HDL on osteocalcin (OCN) expression in monocyte cell lines through SR-B1. BLT-1 may be used to study cell signaling pathways that have role in cholesterol influx and efflux.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic nitrogen compounds
Class Organonitrogen compounds
Subclass Hydrazines and derivatives
Intermediate Tree Nodes Thiosemicarbazides
Direct Parent Thiosemicarbazones
Alternative Parents Organosulfur compounds  Hydrocarbon derivatives  
Molecular Framework Aliphatic homomonocyclic compounds
Substituents Thiosemicarbazone - Hydrocarbon derivative - Organosulfur compound - Aliphatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as thiosemicarbazones. These are compounds containing the thiosemicarbazone functional group obtained by replacing the carbonyl group by a thiocarbonyl group.
External Descriptors Not available

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name [(E)-(2-hexylcyclopentylidene)amino]thiourea
INCHI InChI=1S/C12H23N3S/c1-2-3-4-5-7-10-8-6-9-11(10)14-15-12(13)16/h10H,2-9H2,1H3,(H3,13,15,16)/b14-11+
InChIKey OWGUSBISUVLUJF-SDNWHVSQSA-N
Smiles CCCCCCC1CCCC1=NNC(=S)N
Isomeric SMILES CCCCCCC\1CCC/C1=N\NC(=S)N
WGK Germany 3
Molecular Weight 241.4
Reaxy-Rn 11250336
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11250336&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number Certificate Type Date Item
A2420068 Certificate of Analysis Dec 19, 2023 B412587
A2420069 Certificate of Analysis Dec 19, 2023 B412587
A2420070 Certificate of Analysis Dec 19, 2023 B412587
A2420071 Certificate of Analysis Dec 19, 2023 B412587
A2420072 Certificate of Analysis Dec 19, 2023 B412587

Chemical and Physical Properties

Solubility DMSO: ≥13 mg/mL
Molecular Weight 241.400 g/mol
XLogP3 3.300
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 6
Exact Mass 241.161 Da
Monoisotopic Mass 241.161 Da
Topological Polar Surface Area 82.500 Ų
Heavy Atom Count 16
Formal Charge 0
Complexity 251.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 1
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 1

Solution Calculators

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