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130

抑制剂 & 化合物

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Cat. No. Product Name Target Signaling Pathways
T4578 Tipranavir

PNU-140690

SARS-CoV; HIV Protease Microbiology/Virology; Proteases/Proteasome
Tipranavir 是一种蛋白酶抑制剂,对1种以上蛋白酶抑制剂耐药的HIV-1具有抑制作用 。Tipranavir 可有效抑制 HIV-1 蛋白酶 酶活性和二聚化,对抗多种蛋白酶抑制剂(PI)的HIV-1分离株具有有效的活性(IC50 为 66-410 nM)。Tipranavir 对SARS-CoV-2 3CLpro 活性有抑制作用。
T80672 1,4-Dihydroxynaphthalene

Naphthalene-1,4-diol

HSV Microbiology/Virology
1,4-Dihydroxynaphthalene 一种有效的 HSV-1蛋白酶抑制剂,对HCMV蛋白酶有抑制作用,可用于研究疱疹病毒。
T13268 USP7-IN-1

DUB Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
USP7-IN-1 是泛素蛋白特异性蛋白酶的选择性、可逆性抑制剂,IC50为 77 μM,可用于癌症研究。
T4338 USP7/USP47 inhibitor

USP7/47 inhibitor-1

DUB Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
USP7/USP47 inhibitor (USP7/47 inhibitor-1) 是一种选择性泛素特异性蛋白酶 7/47 抑制剂,EC50值分别为 0.42 μM 和 1.0 μM。
T4317 PF 429242

NPC1L1; Lipid Membrane transporter/Ion channel; Metabolism
PF 429242 是甾醇调节元件结合蛋白 (SREBP) 位点 1 蛋白酶的竞争性抑制剂 (IC50 = 0.175 μM)。它对位点 1 蛋白酶对一组丝氨酸蛋白酶具有选择性。 PF-429242 抑制 CHO 细胞中胆固醇的合成速率 (IC50 = 0.53 μM)。
T1623 Lopinavir

ABT-378,洛匹那韦

SARS-CoV; HIV Protease Microbiology/Virology; Proteases/Proteasome
Lopinavir (ABT-378) 是一种选择性肽模拟 HIV-1 蛋白酶的高效抑制剂。它通过阻止 HIV-1 的成熟而起作用,从而阻断其感染性。它也是 SARS-CoV 3CLpro 的抑制剂。
T9216 MLT-943

MLT943

MALT Immunology/Inflammation
ML-943 是选择性的、口服活性的MALT1 protease 抑制剂。它可抑制 PBMC 或全血中 IL-2 的分泌,PBMC 中抑制的IC50值为 0.07~0.09 μM,全血中抑制的IC50值为 0.6~0.8 μM)。它具有抗炎作用,可用于研究 FcgR 介导的炎症。
T22168 Vialinin A

Terrestrin A

DUB Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
Vialinin A (Terrestrin A) (Terrestrin A) 是一种具有抗氧化性质的对三苯化合物。Vialinin A (Terrestrin A) 是 TNF-α,USP4, USP5 和 SENP1 特异性蛋白酶 1 的有效抑制剂。Vialinin A (Terrestrin A) 可用于自身免疫疾病和癌症研究。
T9458 PF-00835231

SARS-CoV Microbiology/Virology
PF-00835231 是一种 CoV-2 半胱氨酸 3C 样蛋白酶抑制剂,对 SARS CoV-2 和 SARS CoV-1 3CLpro 的 IC50 分别为 0.27 nM 和 4 nM。它用于抗 SARS-CoV-2/COVID-19 的研究。
T12926 SJB3-019A

Others; DUB Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others; Ubiquitination
SJB3-019A 是一种有效的、有效的和新型的泛素特异性蛋白酶1(USP1)抑制剂,在 K562细胞中促进 ID1降解和细胞毒性的作用是 SJB2-043的5倍,IC50为0.0781 μM。SJB3-019A 抑制细胞增殖,使细胞凋亡。
T24362 L 756423

L756423,MK-944a,MK944a,L-756,423,L-756423,MK 944a

HIV Protease Microbiology/Virology; Proteases/Proteasome
L 756423 (L756423) 是一种新型有效且具有选择性和竞争性的HIV蛋白酶抑制剂,对 HIV-1 PR 的 Ki 值为0.049 nM。L 756423 能阻止HIV(IIIb)感染的 MT25 淋巴细胞在0.50-0.1nM处的扩散,可用于研究获得性免疫缺陷综合征(AIDS)。
T3226 Paritaprevir free base

ABT-450,Veruprevir,帕利瑞韦

HCV Protease Microbiology/Virology; Proteases/Proteasome
Paritaprevir free base (ABT-450) 是一种口服生物可利用的合成酰基磺酰胺抑制剂,可抑制丙型肝炎病毒 (HCV) 蛋白酶复合物,由非结构蛋白 3 和 4A (NS3/NS4A) 组成,对 HCV 基因型 1 具有潜在活性。 给药后,paritaprevir 可逆地结合 HCV NS3/NS4A 蛋白酶的活性中心和结合位点,并阻止 NS3/NS4A 蛋白酶介导的多蛋白成熟。这会破坏病毒蛋白的加工和病毒复制复合物的形成,从而抑制病毒在 HCV 基因型 1 感染的宿主细胞中的复制。 NS3 是一种丝氨酸蛋白酶,对于 HCV 多蛋白内多个位点的蛋白水解切割至关重要,并且在 HCV 核糖核酸 (RNA) 复制过程中起关键作用。 NS4A 是 NS3 的激活因子。 HCV 是属于黄病毒科的一种小的、有包膜的单链 RNA 病毒,感染与肝细胞癌 (HCC) 的发展有关。
T37173 MPro Inhibitor 11a

MProinhibitor 11a is an inhibitor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (MPro; IC50= 0.053 μM in a TR-FRET assay).1It reduces viral yield in the culture supernatant of SARS-CoV-2-infected Vero E6 cells (EC50= 0.53 μM). MProinhibitor 11a also reduces viral RNA copy numbers in the same model when used at concentrations ranging from 1.85 to 50 μM. 1.Dai, W., Zhang, B., Jiang, X.-M., et al.Structure-based design of antiviral drug candidates targeting the SARS-...
T9574 PF-07304814

Lufotrelvir,卢夫特韦

Lufotrelvir (PF-07304814) 是 PF-00835231 的磷酸盐前药,是一种有效的3CLpro 蛋白酶 (Mpro) 抑制剂,具有 抗SARS-CoV-2 病毒活性。Lufotrelvir 结合并抑制 SARS-CoV-2 3CLpro 活性,Ki 为 174nM。Lufotrelvir 是一种很有前途的单一抗病毒试剂,也可用于与针对冠状病毒生命周期其他关键阶段的其他抗病毒试剂的联合研究。
T36682 USP30 inhibitor 18

DUB Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
USP30 inhibitor 18 是有效的USP30选择性抑制剂,IC50为 0.02 μM。它增加蛋白质泛素化并加速线粒体自噬。
T26446 A 77003

A-77003,Abbott 77003,A77003

A 77003 is a HIV-1 protease inhibitor. A77003 impairs HIV-1 protease-mediated Gag processing.
T26445 A 76889

A76889,A-76889

A 76889 is an inhibitor of HIV-1 protease.
T24008 DMP 323

JCR424,DMP-323,JCR-424,JCR 424,DMP323

DMP 323 is a potent inhibitor of HIV-1 protease.
T70518 CGP-53437

CGP-53437 is a novel HIV-1 protease inhibitor, also potently inhibiting major aspartyl peptidase 1 (May1), a secreted Cryptococcus neoformans protease.
T15683 L-689502

HIV Protease Microbiology/Virology; Proteases/Proteasome
L-689502 is a potent HIV-l protease inhibitor (IC50: 1 nM).
T24266 KNI-1657

KNI-1657 is a potent and selective HIV-1 protease inhibitor (Anti-HIV-1 pNL4-3, EC50: 3 nM). KNI-1657 is a highly potent HIV-1 Protease Inhibitor against Lopinavir.
T36306 FT206

FT206 is a carboxamide inhibitor of ubiquitin-specific protease[1].
T26451 A 80987

A80987,A-80987

A 80987 is an inhibitor of HIV-1 protease.
T24737 Rpi 856 A

Rpi856 A,Rpi 856 B,Rpi-856 A,Rpi-856 B,Rpi856 B

Rpi 856 A is a retrovirus protease inhibitor. It is effective against HIV-1 and HTLV-1 proteases.
T30839 Cgp 53820

Cgp53820,Cgp-53820

CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.
T26440 A 74704

A-74704,A74704

A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.
T13417 ZYZ-488

Others Others
ZYZ-488 is a competitive inhibitor of apoptotic protease activating factor-1 (Apaf-1).
T26128 Rpi 856 C

Rpi-856 C,Rpi856 C,Rpi-856 D,Rpi856 D,Rpi 856 D

Rpi 856 C is a retrovirus protease inhibitor from Streptomyces that is effective against HIV-1 and HTLV-1 proteases.
T30841 Cgp 57813

Cgp-57813,Cgp57813

CGP 57813 is a lipophilic compound, which can be used as an inhibitor of HIV-1 protease.
T40068 SENP1-IN-1

SENP1-IN-1

SENP1-IN-1 is a distinct inhibitor of the deSUMOylation protease 1 (SENP1), designed to enhance tumor radiosensitivity.
T10082 DPP-IV-IN-1

Others Others
DPP-IV-IN-1 is an effective inhibitor of dipeptidyl peptidase IV (DPP-IV), a serine protease (IC50: 4.6 nM).
T63949 HIV-1 protease-IN-2

HIV-1 protease-IN-2 是 HIV-1 protease 的有效抑制剂 (IC50: 2.53 nM)。HIV-1 protease-IN-2 对 DRV (达芦那韦)敏感或耐药性 HIV-1 突变体均表现出抗病毒效果。
T70717 KNI 174

KNI 174 is a new type of anti‐AIDS drug used as an HIV‐1 protease inhibitor
T28306 PD 099560

PD099560,PD-099560

PD 099560 is a non-peptide inhibitor of HIV-1 protease, a significant target enzyme in AIDS research.
T40067 SENP1-IN-4

SENP1-IN-4

SENP1-IN-4, a distinct inhibitor of the deSUMOylation protease 1 (SENP1), is designed to enhance tumor radiosensitivity.
T40066 SENP1-IN-3

SENP1-IN-3

SENP1-IN-3 is a distinct inhibitor of the deSUMOylation protease 1 (SENP1), designed to enhance tumor radiosensitivity.
T40069 SENP1-IN-2

SENP1-IN-2

SENP1-IN-2, a distinct inhibitor of the deSUMOylation protease 1 (SENP1), is designed to enhance tumor radiosensitivity.
T14295 Antipain

Others Others
Antipain is a protease inhibitor isolated from Actinomycetes. Antipain inhibits N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced transformation and increases chromosomal aberrations[1][2].
T30585 Brecanavir

GW-640385,GW-640385X,UNII-E367I8C7FI,CHEMBL206031,GW-0385

Brecanavir is a tyrosyl-based arylsulfonamide, high affinity, protease inhibitor (PI) for the treatment of human immunodeficiency virus type 1.
T15163 DPC-681

DPH-153893

Others Others
DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).
T74939 HIV protease-IN-1

HIVprotease-IN-1 (compound 1·succinate) 是一种有效的HIV 蛋白酶 (HIV protease) 非肽抑制剂,可用于艾滋病的研究。
T63453 HIV-1 protease-IN-1

HIV-1 protease-IN-1 是 HIV-1 蛋白酶的有效抑制剂 (IC50: 90 pM)。HIV-1 protease-IN-1 对 B-HIV 具有抗病毒活性 (EC50: 89 nM)。HIV-1 protease-IN-1 能够作用于 C-HIV 毒株 ZM246 (EC50: 13.59 nM) 以及 C-HIV 株 Indie (EC50: 8.23 nM)。
T14187 ALLM

Calpain inhibitor II

Others Others
ALLM (Calpain inhibitor II), a potent calpain and cathepsin protease inhibitor, not only prevents neuronal cell death but also enhances chronic neurological function following spinal cord injury (SCI)[1][2].
T35043 Vedroprevir

GS9451,GS 9451,GS-9451

Vedroprevir, also known as GS9451, is a selective hepatitis C virus (HCV) NS3 protease inhibitor in the development of the treatment of genotype 1 (GT1) HCV infection.
T63733 HIV-1 protease-IN-6

HIV-1 protease-IN-6 (compound 17d) 是 HIV-1 蛋白酶 (HIV-1 protease) 的有效抑制剂 (IC50: 21 pM, Ki: 4.7 pM)。HIV-1 protease-IN-6 对 DRV (darunavir) 耐药病毒突变体具有显著的抗病毒效果 (antiviral activity),抑制强度甚至超过对野生型病毒。
T8675 Vaniprevir

Others Others
Vaniprevir is a macrocyclic hepatitis C virus NS3/4a protease inhibitor and is active against both the genotype 1 and genotype 2 NS3/4a protease enzymes. vaniprevir has good plasma exposure and excellent liver exposure in multiple species.
T76603 HIV-IN petide

HIV-IN petide 是HIV-1蛋白酶 (Ki=50 nM) 的竞争性抑制剂。
T38931 Calpain Inhibitor-1

Calpain Inhibitor-1 (compound 36) is a highly potent and selective inhibitor of Calpain 1 (Cal1), which is a cysteine protease. It exhibits an IC50 value of 100 nM and a Ki value of 2.89 μM.
T75871 FSLLRY-NH2 TFA

FSLLRY-NH2 TFA 是蛋白酶激活受体2(PAR2)抑制剂。
T79295 HIV-1 protease-IN-9

HIV Protease Microbiology/Virology; Proteases/Proteasome
HIV-1protease-IN-9 (compound 5b)为HIV-1蛋白酶抑制剂,具有0.028 nM的Ki值和66.8 nM的IC50,表现出显著的抗病毒活性。

化合物

Tipranavir
Cat.No: T4578
Synonym: PNU-140690
Target: SARS-CoV, HIV Protease
1,4-Dihydroxynaphthalene
Cat.No: T80672
Synonym: Naphthalene-1,4-diol
Target: HSV
USP7-IN-1
Cat.No: T13268
Synonym:
Target: DUB
USP7/USP47 inhibitor
Cat.No: T4338
Synonym: USP7/47 inhibitor-1
Target: DUB
PF 429242
Cat.No: T4317
Synonym:
Target: NPC1L1, Lipid
Lopinavir
Cat.No: T1623
Synonym: ABT-378,洛匹那韦
Target: SARS-CoV, HIV Protease
MLT-943
Cat.No: T9216
Synonym: MLT943
Target: MALT
Vialinin A
Cat.No: T22168
Synonym: Terrestrin A
Target: DUB
PF-00835231
Cat.No: T9458
Synonym:
Target: SARS-CoV
SJB3-019A
Cat.No: T12926
Synonym:
Target: Others, DUB
L 756423
Cat.No: T24362
Synonym: L756423,MK-944a,MK944a,L-756,423,L-756423,MK 944a
Target: HIV Protease
Paritaprevir free base
Cat.No: T3226
Synonym: ABT-450,Veruprevir,帕利瑞韦
Target: HCV Protease
MPro Inhibitor 11a
Cat.No: T37173
Synonym:
Target:
PF-07304814
Cat.No: T9574
Synonym: Lufotrelvir,卢夫特韦
Target:
USP30 inhibitor 18
Cat.No: T36682
Synonym:
Target: DUB
A 77003
Cat.No: T26446
Synonym: A-77003,Abbott 77003,A77003
Target:
A 76889
Cat.No: T26445
Synonym: A76889,A-76889
Target:
DMP 323
Cat.No: T24008
Synonym: JCR424,DMP-323,JCR-424,JCR 424,DMP323
Target:
CGP-53437
Cat.No: T70518
Synonym:
Target:
L-689502
Cat.No: T15683
Synonym:
Target: HIV Protease
KNI-1657
Cat.No: T24266
Synonym:
Target:
FT206
Cat.No: T36306
Synonym:
Target:
A 80987
Cat.No: T26451
Synonym: A80987,A-80987
Target:
Rpi 856 A
Cat.No: T24737
Synonym: Rpi856 A,Rpi 856 B,Rpi-856 A,Rpi-856 B,Rpi856 B
Target:
Cgp 53820
Cat.No: T30839
Synonym: Cgp53820,Cgp-53820
Target:
A 74704
Cat.No: T26440
Synonym: A-74704,A74704
Target:
ZYZ-488
Cat.No: T13417
Synonym:
Target: Others
Rpi 856 C
Cat.No: T26128
Synonym: Rpi-856 C,Rpi856 C,Rpi-856 D,Rpi856 D,Rpi 856 D
Target:
Cgp 57813
Cat.No: T30841
Synonym: Cgp-57813,Cgp57813
Target:
SENP1-IN-1
Cat.No: T40068
Synonym: SENP1-IN-1
Target:
DPP-IV-IN-1
Cat.No: T10082
Synonym:
Target: Others
HIV-1 protease-IN-2
Cat.No: T63949
Synonym:
Target:
KNI 174
Cat.No: T70717
Synonym:
Target:
PD 099560
Cat.No: T28306
Synonym: PD099560,PD-099560
Target:
SENP1-IN-4
Cat.No: T40067
Synonym: SENP1-IN-4
Target:
SENP1-IN-3
Cat.No: T40066
Synonym: SENP1-IN-3
Target:
SENP1-IN-2
Cat.No: T40069
Synonym: SENP1-IN-2
Target:
Antipain
Cat.No: T14295
Synonym:
Target: Others
Brecanavir
Cat.No: T30585
Synonym: GW-640385,GW-640385X,UNII-E367I8C7FI,CHEMBL206031,GW-0385
Target:
DPC-681
Cat.No: T15163
Synonym: DPH-153893
Target: Others
HIV protease-IN-1
Cat.No: T74939
Synonym:
Target:
HIV-1 protease-IN-1
Cat.No: T63453
Synonym:
Target:
ALLM
Cat.No: T14187
Synonym: Calpain inhibitor II
Target: Others
Vedroprevir
Cat.No: T35043
Synonym: GS9451,GS 9451,GS-9451
Target:
HIV-1 protease-IN-6
Cat.No: T63733
Synonym:
Target:
Vaniprevir
Cat.No: T8675
Synonym:
Target: Others
HIV-IN petide
Cat.No: T76603
Synonym:
Target:
Calpain Inhibitor-1
Cat.No: T38931
Synonym:
Target:
FSLLRY-NH2 TFA
Cat.No: T75871
Synonym:
Target:
HIV-1 protease-IN-9
Cat.No: T79295
Synonym:
Target: HIV Protease
Cat. No. Product Name Target Signaling Pathways
T4S0181 Hinokiflavone

日本扁柏黄酮,扁柏双黄酮

MMP; BCL; E1/E2/E3 Enzyme Apoptosis; Proteases/Proteasome; Ubiquitination
Hinokiflavone 是pre-mRNA 剪接活性的新型调节剂,通过抑制剪接体装配来阻止pre-mRNA 底物的剪接,特别是阻止 B complex 的形成。它是SUMO protease 蛋白酶抑制剂,能够抑制前哨蛋白特异性蛋白酶 1 的活性。
TN1059 Ganoderic acid B

IL Receptor; HIV Protease; JAK; STAT Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Proteases/Proteasome; Stem Cells
Ganoderic acid B 是从灵芝中分离的一种三萜类天然产物。它是端粒酶抑制剂,抑制 Epstein-Barr 病毒抗原的活化。它是 HIV-1 蛋白酶抑制剂。
TN5171 Tricetin

Apoptosis; Others; Nrf2 Apoptosis; Immunology/Inflammation; Others
Tricetin 是一种从石榴中分离出的类黄酮。Tricetin 是 Keap1-Nrf2 蛋白相互作用(PPI)的强效竞争性抑制剂,通过激活 Nrf2/HO-1 信号通路和阻止线粒体依赖性细胞凋亡通路,保护帕金森病患免受 6-OHDA 诱导的神经毒性的影响。Tricetin 通过 Akt/GSK-1β途径抑制鼻咽癌的迁移和指示性蛋白酶早老素-1(PS-1)表达。Tricetin 抑制由Egr-1介导的氧化LDL 诱导的内皮炎症,保护大鼠软骨细胞免受IL-1β诱导的炎症和细胞凋亡。
T5S0983 Absinthin

Absinthiin,Absynthin,洋艾素

HIV Protease Microbiology/Virology; Proteases/Proteasome
Absinthin (Absynthin) 是结构独特的三萜类化合物,是艾草苦味高的原因。它是苦味受体hTAS2R46的激动剂,它利用 hTAS2R46 介导的受体特异性机制抑制组胺诱导的细胞内 Ca2+升高。
TN4347 Jacoumaric acid

HIV Protease Microbiology/Virology; Proteases/Proteasome
Jacoumaric acid is a lead molecule from the library or database of natural compounds as a HIV-1 protease inhibitor.
T10928 Cytochalasin A

HIV Protease Microbiology/Virology; Proteases/Proteasome
Cytochalasin A is a cell-permeable fungal toxin and is an oxidized derivative of cytochalasin B. Cytochalasin A is an inhibitor of HIV-1 protease (IC50 = 3 μM), inhibits actin polymerization and interferes with microtubule assembly by reacting with sulfhy
T73900 (±)-Alliin

(±)-Alliin 是大蒜的主要活性成分。(±)-Alliin 被认为是SARS-CoV-2 (Mpro)的虚拟抑制剂。
T75648 Rivulariapeptolides 1155

Rivulariapeptolides 1155 是一种有效的丝氨酸蛋白酶 (serine protease) 抑制剂,对糜蛋白酶、弹性蛋白酶、蛋白蛋白酶 K 的 IC50分别为 41.84、4.94、56.54 nM。
T79947 10-Hydroxyaloin A

SARS-CoV Microbiology/Virology
10-Hydroxyaloin A有效抑制SARS-CoV-2,与SARS-CoV-2 Mpro活性位点显著结合。
T75649 Rivulariapeptolides 1185

Rivulariapeptolides 1185 是一种高效的选择性丝氨酸蛋白酶抑制剂,其对胰凝蛋白酶、弹性蛋白酶和蛋白酶 K 的 IC50分别为 13.17 nM、23.59 nM 和 55.26 nM。
T75651 Rivulariapeptolides 988

Rivulariapeptolides 988作为一种高效选择性丝氨酸蛋白酶抑制剂,对胰凝蛋白酶、弹性蛋白酶和蛋白酶K的IC50分别为95.46 nM、15.29 nM和85.50 nM。
T75652 Molassamide B

Molassamide B,丝氨酸蛋白酶抑制剂,对胰凝乳蛋白酶、弹性蛋白酶及蛋白酶 K 具有显著抑制活性,其IC50值分别为24.65、11.69和5.42 nM。
T75650 Rivulariapeptolides 1121

Rivulariapeptolides 1121,作为一种高效的选择性丝氨酸蛋白酶抑制剂,对胰凝蛋白酶、弹性蛋白酶和蛋白酶K展示出了显著的抑制活性,其IC50值分别为35.52 nM、13.24 nM和48.05 nM。
T72508 Palmatine hydroxide

Palmatine hydroxide 是不可逆的口服活性IDO-1抑制剂,其对HEK 293-hIDO-1 和 rhIDO-1的IC50值分别为3 μM和157 μM。该化合物还能非竞争性抑制(WNV)NS2B-NS3蛋白酶,IC50值为96 μM。Palmatine hydroxide展现了抗癌、抗炎、神经保护、抗细菌和抗病毒的活性。

天然产物

Hinokiflavone
Cat.No: T4S0181
Synonym: 日本扁柏黄酮,扁柏双黄酮
Target: MMP, BCL, E1/E2/E3 Enzyme
Ganoderic acid B
Cat.No: TN1059
Synonym:
Target: IL Receptor, HIV Protease, JAK, STAT
Tricetin
Cat.No: TN5171
Synonym:
Target: Apoptosis, Others, Nrf2
Absinthin
Cat.No: T5S0983
Synonym: Absinthiin,Absynthin,洋艾素
Target: HIV Protease
Jacoumaric acid
Cat.No: TN4347
Synonym:
Target: HIV Protease
Cytochalasin A
Cat.No: T10928
Synonym:
Target: HIV Protease
(±)-Alliin
Cat.No: T73900
Synonym:
Target:
Rivulariapeptolides 1155
Cat.No: T75648
Synonym:
Target:
10-Hydroxyaloin A
Cat.No: T79947
Synonym:
Target: SARS-CoV
Rivulariapeptolides 1185
Cat.No: T75649
Synonym:
Target:
Rivulariapeptolides 988
Cat.No: T75651
Synonym:
Target:
Molassamide B
Cat.No: T75652
Synonym:
Target:
Rivulariapeptolides 1121
Cat.No: T75650
Synonym:
Target:
Palmatine hydroxide
Cat.No: T72508
Synonym:
Target:
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