(-)-Calanolide B
(-)-Calanolide B is a non-nucleoside reverse transcriptase (NNRT) inhibitor with an IC50 of 0.5 mM against HIV-1 RT. (-)-Calanolide B inhibits the replication of HIV-1 IIIb/LAV. (-)-Calanolide B is applicable to research related to HIV-1 infection.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- CAS. Nr.: 909-14-8
- Formel: C22H26O5
- Molecular Weight:370.44
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
Beschreibung
IC50 & Target
[1]|
HIV-1 RT 0.5 mM (IC50) |
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| CCRF-CEM | IC50 |
18.7 μM
Compound: (-)-1
|
Anti-HIV activity against HIV-I RFII strain in CEM cell line
Anti-HIV activity against HIV-I RFII strain in CEM cell line
|
[PMID: 8632437] |
| CEM-SS | EC50 |
0.2 μM
Compound: 2
|
Using the XTT assay for cell viability, effective concentration to protect human lymphoblastoid CEM-SS cells from the cytopathic effects of HIV-1 (RF strain) was determined
Using the XTT assay for cell viability, effective concentration to protect human lymphoblastoid CEM-SS cells from the cytopathic effects of HIV-1 (RF strain) was determined
|
[PMID: 8893846] |
| CEM-SS | IC50 |
5.9 μM
Compound: 2
|
Using the XTT assay for cell viability, inhibitory concentration to protect human lymphoblastoid CEM-SS cells from the cytopathic effects of HIV-1 (RF strain) was determined
Using the XTT assay for cell viability, inhibitory concentration to protect human lymphoblastoid CEM-SS cells from the cytopathic effects of HIV-1 (RF strain) was determined
|
[PMID: 8893846] |
| CEM-SS | EC50 |
0.2 μM
Compound: (-)-Calanolide B
|
Antiviral activity against HIV1 RF in human CEM-SS cells assessed as inhibition of virus-induced cytopathic effect
Antiviral activity against HIV1 RF in human CEM-SS cells assessed as inhibition of virus-induced cytopathic effect
|
[PMID: 11430019] |
| H9 | EC50 |
0.22 μM
Compound: 13
|
Antiviral activity against HIV1 infected in human H9 cells assessed as effect on virus-induced cytopathic effect by tetrazolium/formazan assay
Antiviral activity against HIV1 infected in human H9 cells assessed as effect on virus-induced cytopathic effect by tetrazolium/formazan assay
|
[PMID: 8792623] |
| H9 | IC50 |
9.8 μM
Compound: 13
|
Cytotoxicity against human H9 cells
Cytotoxicity against human H9 cells
|
[PMID: 8792623] |
| MT2 | IC50 |
5.89 μM
Compound: (-)-1
|
Anti-HIV activity against HIV-I A17 strain in MT2 cell line
Anti-HIV activity against HIV-I A17 strain in MT2 cell line
|
[PMID: 8632437] |
| MT2 | IC50 |
6.16 μM
Compound: (-)-1
|
Anti-HIV activity against HIV-I G910-6 strain in MT2 cell line
Anti-HIV activity against HIV-I G910-6 strain in MT2 cell line
|
[PMID: 8632437] |
| MT2 | IC50 |
6.21 μM
Compound: (-)-1
|
Anti-HIV activity against HIV-I H112-2 strain in MT2 cell line
Anti-HIV activity against HIV-I H112-2 strain in MT2 cell line
|
[PMID: 8632437] |
| MT2 | IC50 |
7.31 μM
Compound: (-)-1
|
Anti-HIV activity against HIV-I IIIB strain in MT2 cell line
Anti-HIV activity against HIV-I IIIB strain in MT2 cell line
|
[PMID: 8632437] |
In Vitro
Chemical Information
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CAS. Nr. 909-14-8
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Molecular Weight 370.44
-
Formel C22H26O5
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SMILES
CCCC(C1=C(O2)C3=C(O[C@H]([C@@H]([C@@H]3O)C)C)C4=C1OC(C)(C=C4)C)=CC2=O
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Structure Classification
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Initial Source
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Versand
Room temperature in continental US; may vary elsewhere.
-
Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Protokoll
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Research Protocol for Infectious Diseases
Infectious-disease experiments test how pathogens interact with host barriers, innate immune receptors, inflammatory signaling, pathogen replication, and tissue injury; pattern-recognition receptors such as TLRs, RIG-I-like receptors, NOD-like receptors, and inflammasomes detect microbial molecules and activate NF-κB, interferon, and cytokine responses. The central hypothesis is that infection severity reflects the balance between pathogen burden and host response: protective inflammation restricts pathogen growth, whereas excessive or mislocalized inflammation contributes to tissue damage and disease phenotype. Unresolved questions include which host pathways are protective versus pathogenic, why some infection models fail to translate to human disease, and which combined readouts best predict clinically relevant infection outcomes.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)