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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 321673-30-7 Chemical Structure| 321673-30-7

Structure of BLT-1
CAS No.: 321673-30-7

Chemical Structure| 321673-30-7

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BLT-1 is a specific inhibitor of the SR-BI (Scavenger receptor, class B, type I) mediated lipid transfer. The compound inhibits both cellular selective lipid uptake of HDL cholesteryl ether and efflux of cellular cholesterol to HDL.

Synonyms: Block lipid transport-1

4.5 *For Research Use Only !

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Product Details of BLT-1

CAS No. :321673-30-7
Formula : C12H23N3S
M.W : 241.40
SMILES Code : S=C(N)N/N=C1C(CCCCCC)CCC\1
Synonyms :
Block lipid transport-1
MDL No. :MFCD00571007

Safety of BLT-1

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P501-P270-P264-P301+P310+P330-P405
Class:6.1
UN#:2811
Packing Group:

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
COS7 cells 10 μM 1 hour BLT-1 inhibits SR-B1-mediated HDL-CE uptake but does not affect fatty acid uptake PMC6957692
HEK293 cells 10 μM 1 hour BLT-1 inhibits SR-B1-mediated HDL-CE uptake but does not affect fatty acid uptake PMC6957692
J774 macrophages 1 μM 2 hours To block SR-BI mediated cholesterol efflux PMC2866499
PCNSL cell lines (HKBML, TK) 10 µM 24 hours Inhibited lymphoma cell proliferation PMC9207360
COS cells 1 μM 1 hour Assess the effect of BLT-1 on HDL binding and lipid uptake activities of SR-BI mutants (C251S, C384S, C251/384S), showing complete resistance of C384S mutant to BLT-1 PMC3145699
LdlA[SR-BI] cells 1 μM 1 hour Evaluate the inhibitory effect of BLT-1 on SR-BI-mediated DiI-HDL lipid uptake, showing that BLT-1 inhibition of SR-BI is essentially irreversible PMC3145699
Human monocyte-derived macrophages (HMDMs) 10 μM 1 hour BLT-1 treatment increased miR-223-3p export to HDL in HMDMs PMC7477814
Polymorphonuclear neutrophils (PMNs) 10 μM 1 hour Chemical inhibition of cholesterol flux by BLT-1 inhibited HDL-induced pri-mir-223 expression in PMNs PMC7477814
Caco-2 cells 10 μM 2 hours To investigate the effect of BLT-1 on vitamin K uptake, results showed that BLT-1 significantly reduced the uptake of vitamin K. PMC6150738
P. falciparum (3D7 line) 500 μg/ml 24 hours To study HDL uptake and its competitive inhibition, HDL uptake was competitively inhibited by unlabeled HDL PMC8631964
B cell lymphoma cell lines (DAUDI, BALL1, TL-1, RAJI, SLVL) 10 µM 24 hours Inhibited lymphoma cell proliferation PMC9207360
ATLL cell lines (ATN-1, ED, ATL-T, ATL-2s, ATL-35T, MT-1) 10 µM 24 hours Inhibited lymphoma cell proliferation and induced apoptosis PMC9207360
HCMEC/D3 cells 1 µM 4 hours To evaluate the effect of BLT-1 on HDL-mediated protection of BBB integrity, showing that 1 µM BLT-1 partially counteracted the protective effects of HDLs PMC7796353
Primary bovine umbilical vein endothelial cells (BUVEC) 2 μM 48 hours To study the effect of BLT-1 on the proliferation of E. bovis and E. arloingi, results showed that BLT-1 significantly inhibited the replication of these parasites. PMC8622581
African green monkey kidney epithelial cells (MARC 145) 0.25-2 μM 48 hours To study the effect of BLT-1 on the proliferation of T. gondii, N. caninum, and B. besnoiti, results showed that BLT-1 significantly inhibited the replication of these parasites. PMC8622581

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
SCID mice Subcutaneous ED cell lymphoma model Intraperitoneal injection 20 mg/kg Administered daily from day 14 to day 32 Significantly suppressed tumor development and prolonged survival PMC9207360

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.14mL

0.83mL

0.41mL

20.71mL

4.14mL

2.07mL

41.43mL

8.29mL

4.14mL

References

 

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