1. Anti-infection
  2. HIV
  3. L-870810

L-870810 是一种有效的 HIV-1 IN 链转移抑制剂,具有抗病毒活性。

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L-870810 Chemical Structure

L-870810 Chemical Structure

CAS No. : 410544-95-5

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

L-870810 is a potent HIV-1 IN chain transfer inhibitor with antiviral activity[1].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
C8166 CC50
123 μM
Compound: L-870810
Cytotoxicity against human C8166 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against human C8166 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 27810592]
C8166 CC50
132 μM
Compound: I-4, L-870810
Toxicity against human C8166 cells incubated for 72 hrs by MTT assay
Toxicity against human C8166 cells incubated for 72 hrs by MTT assay
[PMID: 23098137]
C8166 EC50
2.33 nM
Compound: L-870810
Antiviral activity against HIV1 3B infected in human C8166 cells assessed as reduction in virus-induced cytopathic effect by MTT assay
Antiviral activity against HIV1 3B infected in human C8166 cells assessed as reduction in virus-induced cytopathic effect by MTT assay
[PMID: 27810592]
C8166 EC50
5 nM
Compound: I-4, L-870810
Antiviral activity against HIV1 3B infected in human C8166 cells assessed as reduction in virus-induced cytopathogenicity measured after 3 days by syncytium reduction assay
Antiviral activity against HIV1 3B infected in human C8166 cells assessed as reduction in virus-induced cytopathogenicity measured after 3 days by syncytium reduction assay
[PMID: 23098137]
HCT-116 IC50
2 μM
Compound: I-4, L-870810
Cytotoxicity against p53 expressing human HCT116 cells incubated for 72 hrs by MTT assay
Cytotoxicity against p53 expressing human HCT116 cells incubated for 72 hrs by MTT assay
[PMID: 23098137]
HCT-116 IC50
2 μM
Compound: I-4, L-870810
Cytotoxicity against p53 deficient human HCT116 cells incubated for 72 hrs by MTT assay
Cytotoxicity against p53 deficient human HCT116 cells incubated for 72 hrs by MTT assay
[PMID: 23098137]
Lymphocyte CC50
2100 nM
Compound: L-870810
Cytotoxicity against human T lymphocyte cells infected with HIV1 BAL by XTT method in presence of 10% FBS
Cytotoxicity against human T lymphocyte cells infected with HIV1 BAL by XTT method in presence of 10% FBS
[PMID: 19104010]
Lymphocyte EC50
3 nM
Compound: L-870810
Antiviral activity against 0.001 MOI HIV1 BAL infected in human T lymphocyte cells by p24 antigen ELISA in presence of 10% FBS
Antiviral activity against 0.001 MOI HIV1 BAL infected in human T lymphocyte cells by p24 antigen ELISA in presence of 10% FBS
[PMID: 19104010]
Lymphocyte EC50
60 nM
Compound: L-870810
Antiviral activity against 0.001 MOI HIV1 BAL infected in human T lymphocyte cells by p24 antigen ELISA in presence of 10% FBS, HSA and alpha1-AGP
Antiviral activity against 0.001 MOI HIV1 BAL infected in human T lymphocyte cells by p24 antigen ELISA in presence of 10% FBS, HSA and alpha1-AGP
[PMID: 19104010]
MCF7 IC50
2 μM
Compound: I-4, L-870810
Cytotoxicity against human MCF7 cells incubated for 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells incubated for 72 hrs by MTT assay
[PMID: 23098137]
MDA-MB-435 IC50
6 μM
Compound: I-4, L-870810
Cytotoxicity against human MDA-MB-435 cells incubated for 72 hrs by MTT assay
Cytotoxicity against human MDA-MB-435 cells incubated for 72 hrs by MTT assay
[PMID: 23098137]
MT2 EC50
2 nM
Compound: L-870810
Antiviral activity against HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 10% FBS
Antiviral activity against HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 10% FBS
[PMID: 19104010]
MT2 EC50
200 nM
Compound: L-870810
Antiviral activity against 0.04 MOI HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 100% human serum
Antiviral activity against 0.04 MOI HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 100% human serum
[PMID: 19104010]
MT2 CC50
3000 nM
Compound: L-870810
Cytotoxicity against human MT2 cells infected with HIV1 3B by three fold dilution method in presence of 10% FBS
Cytotoxicity against human MT2 cells infected with HIV1 3B by three fold dilution method in presence of 10% FBS
[PMID: 19104010]
MT2 EC50
41 nM
Compound: L-870810
Antiviral activity against 0.01 MOI HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 100% human serum
Antiviral activity against 0.01 MOI HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 100% human serum
[PMID: 19104010]
MT2 EC50
43 nM
Compound: L-870810
Antiviral activity against HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 10% FBS, HSA and alpha1-AGP
Antiviral activity against HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 10% FBS, HSA and alpha1-AGP
[PMID: 19104010]
MT2 EC50
96 nM
Compound: L-870810
Antiviral activity against 0.02 MOI HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 100% human serum
Antiviral activity against 0.02 MOI HIV1 3B infected in human MT-2 cells by two fold dilution method in presence of 100% human serum
[PMID: 19104010]
MT4 EC50
0.004 μM
Compound: L-870810
Antiviral activity against HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
Antiviral activity against HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
[PMID: 18378713]
MT4 EC50
0.004 μM
Compound: L-870810
Antiviral activity against HIV 1 NL4.3 harboring integrase L74M mutant infected in human MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
Antiviral activity against HIV 1 NL4.3 harboring integrase L74M mutant infected in human MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
[PMID: 18378713]
MT4 EC50
0.0047 μM
Compound: L-870810
Antiviral activity against HIV1 3B infected in human MT4 cells assessed as reduction of virus-induced cytopathogenicity by MTT assay
Antiviral activity against HIV1 3B infected in human MT4 cells assessed as reduction of virus-induced cytopathogenicity by MTT assay
[PMID: 18351727]
MT4 EC50
0.005 μM
Compound: L-870810
Antiviral activity against HIV 1 3B infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
Antiviral activity against HIV 1 3B infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
[PMID: 18378713]
MT4 EC50
0.007 μM
Compound: L-870810
Antiviral activity against HIV 1 NL4.3 integrase S230N mutant infected in human MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
Antiviral activity against HIV 1 NL4.3 integrase S230N mutant infected in human MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
[PMID: 18378713]
MT4 EC50
0.018 μM
Compound: L-870810
Antiviral activity against HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay after 20 passages selected in presence of compound
Antiviral activity against HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay after 20 passages selected in presence of compound
[PMID: 18378713]
MT4 EC50
0.064 μM
Compound: L-870810
Antiviral activity against HIV 1 RIN HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay after 40 passages selected in presence of compound
Antiviral activity against HIV 1 RIN HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay after 40 passages selected in presence of compound
[PMID: 18378713]
MT4 EC50
0.073 μM
Compound: L-870810
Antiviral activity against HIV 1 NL4.3 integrase E92Q mutant infected in human MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
Antiviral activity against HIV 1 NL4.3 integrase E92Q mutant infected in human MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
[PMID: 18378713]
MT4 EC50
0.11 μM
Compound: L-870810
Antiviral activity against HIV 1 3B harboring integrase E92Q S230N double mutant infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 20 passages in presence of compound
Antiviral activity against HIV 1 3B harboring integrase E92Q S230N double mutant infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 20 passages in presence of compound
[PMID: 18378713]
MT4 EC50
0.17 μM
Compound: L-870810
Antiviral activity against HIV 1 3B harboring integrase L34M mutant infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 40 passages in presence of compound
Antiviral activity against HIV 1 3B harboring integrase L34M mutant infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 40 passages in presence of compound
[PMID: 18378713]
MT4 EC50
0.19 μM
Compound: L-870810
Antiviral activity against HIV 1 RIN HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay after 60 passages selected in presence of compound
Antiviral activity against HIV 1 RIN HIV 1 RIN harboring integrase gene infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay after 60 passages selected in presence of compound
[PMID: 18378713]
MT4 EC50
0.55 μM
Compound: L-870810
Antiviral activity against HIV 1 3B harboring integrase E92Q, S230N and L34M triple mutant infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 60 passages in presence of compound
Antiviral activity against HIV 1 3B harboring integrase E92Q, S230N and L34M triple mutant infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 60 passages in presence of compound
[PMID: 18378713]
MT4 IC50
1.1 μM
Compound: L-870810
Antiviral activity against HIV 1 3B infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 50 passages in presence of compound
Antiviral activity against HIV 1 3B infected in MT-4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay selected after 50 passages in presence of compound
[PMID: 18378713]
MT4 CC50
1600 nM
Compound: L-870810
Cytotoxicity against human MT4 cells infected with HIV1 3B by three fold dilution method in presence of 10% FBS
Cytotoxicity against human MT4 cells infected with HIV1 3B by three fold dilution method in presence of 10% FBS
[PMID: 19104010]
MT4 CC50
2.2 μM
Compound: L-870810
Cytotoxicity against human MT4 cells by MTT method
Cytotoxicity against human MT4 cells by MTT method
[PMID: 18351727]
MT4 CC50
2.25 μM
Compound: L-870810
Cytotoxicity against human MT4 cells by MTT assay
Cytotoxicity against human MT4 cells by MTT assay
[PMID: 18541726]
MT4 EC50
4 nM
Compound: L-870810
Antiviral activity against HIV1 3B infected in human MT-4 cells by two fold dilution method in presence of 10% FBS
Antiviral activity against HIV1 3B infected in human MT-4 cells by two fold dilution method in presence of 10% FBS
[PMID: 19104010]
SK-N-MC IC50
28000 nM
Compound: 5, L-870810
Inhibition of CGRP receptor in human SK-N-MC cells assessed as inhibition of CGRP-stimulated cAMP production after 1 hr
Inhibition of CGRP receptor in human SK-N-MC cells assessed as inhibition of CGRP-stimulated cAMP production after 1 hr
[PMID: 21982500]
SUP-T1 EC50
> 1000 nM
Compound: L-870810
Antiviral activity against HIV1 infected in SupT1 cells assessed as accumulation of late RT products after 12 hrs
Antiviral activity against HIV1 infected in SupT1 cells assessed as accumulation of late RT products after 12 hrs
[PMID: 19104010]
SUP-T1 EC50
1.3 nM
Compound: L-870810
Antiviral activity against HIV1 infected in SupT1 cells assessed as accumulation of integrated junction products after 48 hrs by Alu-PCR assay
Antiviral activity against HIV1 infected in SupT1 cells assessed as accumulation of integrated junction products after 48 hrs by Alu-PCR assay
[PMID: 19104010]
分子量

430.45

Formula

C20H19FN4O4S

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献

L-870810 相关分类

  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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L-870810
目录号:
HY-12109
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