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79

抑制剂 & 化合物

21

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Cat. No. Product Name Target Signaling Pathways
T21512 MMP-2/MMP-9 Inhibitor I

MMP Proteases/Proteasome
MMP-2/MMP-9-IN-1 是一种有效的、具有高选择性和可口服的 IV 型胶原酶 (MMP-9MMP-2) 抑制剂,对 MMP-9MMP-2具有抑制作用, IC50分别为 0.24 和 0.3 1μM。MMP-2/MMP-9-IN-1 在肿瘤生长和转移的动物模型中展现出口服活性,可用于研究癌症。
T8310 MMP-9-IN-1

MMP Proteases/Proteasome
MMP-9-IN-1 是特异性的基质金属蛋白酶-9 抑制剂,选择性靶向 MMP-9 的血红素域,对其他 MMP 无影响。
T77617 MMP-9-IN-6

MMP Proteases/Proteasome
MMP-9-IN-6 是一种 MMP-9 抑制剂,其 IC50 值为50 μM, 具有较好的抗溃疡功效。MMP-9-IN-6 具有潜在的抗肿瘤活性,可用于研究组织重塑、伤口修复和动脉粥样硬化。
T36712 BPHA

MMP-2/MMP-9 Inhibitor II

MMP Proteases/Proteasome
BPHA (MMP-2/MMP-9 Inhibitor II) 是一种有效的、具有选择性和口服活性的抑制剂,对MMP-2、MMP-9MMP-14 具有抑制作用,IC50 分别为 12 nM、16 nM 和 17 nM。BPHA 不抑制 MMP-1、-3 和 -7 (IC50 分别为 974、>1000 和 795 nM)。BPHA 具有抗血管生成和抗肿瘤活性。
T37726 MMP-9 Inhibitor I

MMP-9 inhibitor I is an inhibitor of matrix metalloproteinase-9 (MMP-9) that is selective over MMP-1 and MMP-13 (IC50s = 5, 1,050, and 113 nM, respectively). It also decreases the activity of TNF-α converting enzyme (TACE) in a dose-dependent manner (IC50 = 0.54 μM). MMP-9 inhibitor I decreases TNF-α secretion stimulated by LPS in BV-2 microglial cells when used at concentrations of 50 and 100 μM.
T37172 MMP-9/MMP-13 Inhibitor I

MMP-9/MMP-13 Inhibitor I 是 MMP-9MMP-13 双重抑制剂,IC50 均为 0.9 nM。MMP-9/MMP-13 Inhibitor I 对 MMP-9/MMP-13 的选择性是其他 MMP 的 20 倍以上。
T2009 SB-3CT

MMP Proteases/Proteasome
SB-3CT 是一种可透过血脑屏障的、竞争性的金属蛋白酶MMP-2和MMP-9抑制剂,Ki 分别为 13.9 nM、600 nM。他对明胶酶具有高选择性。它具有神经保护和抗癌作用。
T72069 MMP-9-IN-7

MMP-9-IN-7抑制前基质金属蛋白酶活化,可用于预防、治疗或改善 MMP9和/或 MMP13介导的综合征。
T22115 SM-7368

NF-κB NF-κB
NF-κB Activation Inhibitor III 是一种NF-kB 抑制剂,抑制 TNF-α 诱导的MMP-9上调,靶向抑制下游的MAPK p38,可用于靶向 TNF-α 介导的肿瘤侵袭和转移的化疗研究。
TP1015 NFAT Inhibitor

VIVIT peptide

Others Others
NFAT Inhibitor (VIVIT peptide) 是NFAT 的细胞渗透性肽抑制剂,能够选择性抑制钙调磷酸酶介导的NFAT 脱磷酸作用。
T64083 MMP-9-IN-5

MMP-9-IN-5 是一种 MMP-9 抑制剂,其 IC50 值为 4.49 nM,能够与 MMP-9 形成氢键。MMP-9-IN-5 也抑制 AKT 活性,其 IC50 值为 1.34 nM。MMP-9-IN-5 表现出细胞毒性,可诱导细胞凋亡 (apoptosis),能够用于研究癌症。
T63155 MMP-9-IN-3

MMP-9-IN-3 是一种 MMP-9 抑制剂 (IC50: 5.56 nM),可与 MMP-9 形成氢键。MMP-9-IN-3 对 AKT 的活性具有抑制作用 (IC50: 2.11 nM)。MMP-9-IN-3 具有细胞毒性,能够诱导细胞凋亡。MMP-9-IN-3 能够用于研究癌症。
T63994 MMP-9-IN-4

MMP-9-IN-4 是 MMP-9 抑制剂,能够与 MMP-9 形成 H-π 相互作用,IC50 值为 7.46 nM。MMP-9-IN-4 还能够抑制 AKT 活性,其 IC50 值为 8.82 nM。MMP-9-IN-4 能够诱导细胞凋亡 (apoptosis),显示出细胞毒性,能够用于研究癌症。
T81777 MMP-9-IN-8

MMP-9-IN-8(Compound 3)是MMP-9抑制剂,10 μM浓度下抑制活性为42.16%,50 μM时达58.28%。该化合物展现抗癌活性,能诱导MCF-7细胞凋亡,IC50为23.42 μM。
T62555 MMP-2/9-IN-1

MMP-2/9-IN-1 (Compound 4a) 是一种有效的 MMP-2 (IC50: 56 nM) 和 MMP-9 (IC50: 38 nM) 双重抑制剂。MMP-2/9-IN-1 对肿瘤生长具有抑制作用,明显诱导癌细胞凋亡 (apoptosis),抑制细胞迁移,并抑制细胞周期进程导致 DNA 片段化。
T6885 Marimastat

BB2516,马立马司他,KB-R8898,TA2516

MMP Proteases/Proteasome
Marimastat (BB2516) 是一种血管生成和转移抑制剂,限制血管的生长和生成。它是一种广谱的,具有口服活性的MMPs 抑制剂,有效抑制 MMP-9 , MMP-1, MMP-2, MMP-14, MMP-7,用于癌症的研究。
T16966 S 3304

MMP Proteases/Proteasome
S 3304 是一种新型的基质金属蛋白酶抑制剂,能够特异的抑制MMP-2和MMP-9的活性。
TP1741L Histatin 5 acetate

Histatin 5 acetate (115966-68-2 Free base)

MMP Proteases/Proteasome
Histatin 5 acetate 抑制宿主基质金属蛋白酶 MMP-2 和 MMP-9 的活性,IC50 分别为 0.57 和 0.25 μM。
T4783 JNJ0966

MMP Proteases/Proteasome
JNJ0966 是高选择性 MMP-9酶原抑制剂,其 IC50=440 nM。
T61271 MMP2-IN-3

MMP Proteases/Proteasome
MMP2-IN-3是一种有效的基质金属蛋白酶(MMP-2)抑制剂( IC50 值:31 μM)。MMP2-IN-3 抑制 MMP-9MMP-8 ,其 IC50 分别为 26.6 和 32 μM。
T14322 ARP-100

MMP-2 Inhibitor III

MMP Proteases/Proteasome
ARP-100 (MMP-2 Inhibitor III) 是选择性基质金属蛋白酶MMP-2抑制剂 (IC50=12 nM)。它对 MMP-1 (>50 μM),MMP-3 (4.5 μM),MMP-7 (>50 μM) 和MMP-9 (0.2 μM) 的抑制活性较小。它与 MMP-2 的 S1'口袋相互作用,并在体外对基质胶的侵袭模型中显示抗侵袭特性。
TP1501L CTTHWGFTLC, CYCLIC acetate(244082-19-7 free base)

MMP Proteases/Proteasome
CTTHWGFTLC, CYCLIC acetate(244082-19-7 free base) 是基质金属蛋白酶 (MMP)-2 和 MMP-9 的抑制剂。它也被称为IV 型胶原酶或明胶酶。明胶酶是癌症治疗干预的潜在靶点,这些酶的抑制剂可以防止肿瘤进展。
T2743 Ilomastat

Galardin,GM6001,伊洛马司他

MMP Proteases/Proteasome
Ilomastat (GM6001) 是广谱的基质金属蛋白酶 (MMP) 抑制剂,可抑制 MMP 的活性,IC50值分别为 1.5 nM (MMP-1),1.1 nM (MMP-2),1.9 nM (MMP-3),0.5 nM (MMP-9),对人皮肤成纤维细胞胶原酶 (MMP-1) 的Ki=为 0.4 nM。
T6011 Batimastat

巴马司他,BB94

MMP Proteases/Proteasome
Batimastat (BB94) 是广谱MMP 抑制剂,能够抑制MMP-1 (IC50:3 nM),MMP-2 (IC50:4 nM),MMP-9 (IC50:4 nM),MMP-7 (IC50:6 nM) 和 MMP-3 (IC50:20 nM)。
T0407 Edaravone

依达拉奉右莰醇,依达拉奉,MCI-186

Apoptosis; MMP; Free radical scavengers Apoptosis; oxidation-reduction; Proteases/Proteasome
Edaravone (MCI-186) 是一种新型自由基清除剂,能够抑制大鼠与 MMP-9有关的脑出血。
TP1446 Histatin 5 (TFA)(115966-68-2,free)

Histatin 5 (TFA)

MMP Proteases/Proteasome
Histatin 5 (TFA)(115966-68-2,free) (Histatin 5 (TFA)) 抑制宿主基质金属蛋白酶 MMP-2 和 MMP-9 的活性,IC50 分别为 0.57 和 0.25 μM。
T10461 Batimastat sodium salt

BB-94 sodium salt

MMP Proteases/Proteasome
Batimastat (BB-94) sodium salt is a broad-spectrum MMP inhibitor (IC50s: 3, 4, 4, 6, and 20 nM for MMP-1, MMP-2, MMP-9, MMP-7, and MMP-3).
T76618 VPLSLYSG

VPLSLYSG 是一种可被基质金属蛋白酶-9 (MMP-9)、MMP-1和MMP-2降解的八肽。VPLSLYSG 在MMP 底物中有潜在应用。
T28147 ND-378

ND-378 is a potent and selective inhibitor of MMP-2 with no inhibition on MMP-9 and MMP-14.
T13358 XL-784

MMP Proteases/Proteasome
XL-784 is a selective inhibitor of matrix metalloproteinases (MMP)(IC50s of ~1900, 0.81, 120, 10.8, 18, 0.56 nM for MMP-1,MMP-2,MMP-3,MMP-8,MMP-9,MMP-13,respectively).
T12539 Prinomastat hydrochloride

KB-R9896 hydrochloride,AG3340 hydrochloride

MMP Proteases/Proteasome
Prinomastat hydrochloride is a orally active inhibitor of metalloproteinase (MMP)(MMP-1, MMP-3 and MMP-9 with IC50s of 79, 6.3 and 5.0 nM , respectively),with Antitumor avtivity.
T37983 GM 1489

GM 1489 is a broad-spectrum inhibitor of matrix metalloproteinases (MMPs) with Ki values of 0.002, 0.1, 0.5, 0.2, and 20 μM for MMP-1, MMP-8, MMP-2, MMP-9, and MMP-3, respectively. It reduces 5-aza-2'-deoxycytidine-induced increases in MMP-1, MMP-2, MMP-3, MMP-7, MMP-9, and MMP-14 expression as well as cell invasion in AsPC-1, BxPC-3, Hs766T, MiaPaCa2, and PANC-1 cancer cells. Topical administration of GM 1489 (100 μg) inhibits increases in ear thickness and epidermal hyperplasia induced by phor...
T36362 Dnp-PLGMWSR (trifluoroacetate salt)

Dnp-PLGMWSR is a fluorogenic substrate for matrix metalloproteinase-2 (MMP-2) and MMP-9. The activity of MMP-2 and MMP-9 can be quantified by measuring tryptophan fluorescence that is unquenched upon peptide hydrolysis that removes the N-terminal dinitrophenol (Dnp) group.
T36360 Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2

Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2

Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2 is a fluorogenic substrate for matrix metalloproteinase-1 (MMP-1) and MMP-9. Upon cleavage by MMP-1 or MMP-9, N-methylanthranilic acid (Nma) is unquenched and its fluorescence can be used to quantify MMP activity. Nma displays excitation/emission spectra of 340/440 nm, respectively.
T70051 MMI-166

MMI-166 is a selective matrix metalloproteinase (MMP) inhibitor that prevents tumor invasion and metastasis by downregulating the activity of MMP-2 and MMP-9.
T76017 CTTHWGFTLC, CYCLIC TFA

CTTHWGFTLC, CYCLIC TFA 是一种基质金属蛋白酶 MMP-2和MMP-9的环肽抑制剂。对MMP-9的IC50约为 8 μM。
T16986 Tanomastat

BAY 12-9566

MMP Proteases/Proteasome
Tanomastat is an orally bioavailable and non-peptidic biphenyl matrix metalloproteinases inhibitor. For MMP-2, MMP-3, MMP-9, MMP-13 the Ki values are 11, 143, 301, and 1470 nM respectively.
T24775 SD-2590 HCl

SD2590 HCl,SD-2590 Hydrochloride,SD2590 Hydrochloride,SD 2590 Hydrochloride

SD-2590 HCl is an MMP-2,-3, -9, -8, 13, and -14 inhibitor.
T22685 CP-471474

CP 471474

Others Others
Broad spectrum MMP inhibitor (IC<sub>50</sub> values are 0.7, 0.9, 13, 16 and 1170 nM for MMP-2, MMP-13, MMP-9, MMP-3 and MMP-1 respectively). Attenuates early left ventricular dilation after experimental myocardial infarction in mice.
T13357 XL-784 free base

Others Others
XL-784 free base is a selective inhibitor of matrix metalloproteinases (MMP), (IC50s of ~1900, 0.81, 120, 10.8, 18, 0.56 nM for MMP-1,MMP-2,MMP-3,MMP-8,MMP-9,MMP-13,respectively).
T12539L Prinomastat

KB-R9896,普啉司他,AG3340

MMP Proteases/Proteasome
Prinomastat inhibits MMP-2, MMP-3 and MMP-9 (Kis: 0.05 nM, 0.3 nM and 0.26 nM, respectively). Prinomastat crosses the blood-brain barrier. It also has antitumor activity. Prinomastat is a broad-spectrum, potent, orally active metalloproteinase inhibitor (
T75755 Histatin 5 TFA

Histatin 5 TFA 抑制宿主基质金属蛋白酶MMP-2和MMP-9活性,IC50s 分别为 0.57 和 0.25 μM。
T28146 ND-336

ND336,ND-336 hydrochloride,ND 336

ND-336 is a highly selective inhibitor ofMMP-2, MMP-9 and MMP-14. ND-336 accelerates diabetic wound healing by lowering inflammation and by enhancing angiogenesis and re-epithelialization of the wound.
T25925 p-DDAP

pDDAP,p-Dodecylaminophenol

p-DDAP is an anti-invasive agent that acts by significantly suppressing cell invasion, and the activity and mRNA expression of matrix metalloproteinase-9 (MMP-9).
T76269 Dnp-PLGLWA-DArg-NH2 TFA

Dnp-PLGLWA-DArg-NH2 TFA 作为MMP-1和MMP-9的荧光底物,能够用于定量测定MMPs的活性(Ex=280 nm, Em=360 nm)。
T82022 IVMT-Rx-3

NF-κB NF-κB
IVMT-Rx-3是针对SDCBP的PDZ1和PDZ2结构域,特别是MDA-9/Syntenin的抑制剂。该化合物能够中断MDA-9/Syntenin与Src之间的互动,减少NF-κB的激活,并且降低MMP-2/MMP-9的表达量,从而抑制了黑色素瘤的转移。
T69875 ProMMP-9 inhibitor-3c

ProMMP-9 inhibitor-3c is a potent and specific proMMP-9 inhibitor which disrupts f MMP-9 homodimerization and prevents association of proMMP-9 with both α4β1 integrin and CD44 and results in the dissociation of EGFR.
T60551 MMP2-IN-2

MMP2-IN-2 (化合物 42) 是一种有效且选择性的MMP-2(基质金属蛋白酶)抑制剂,其IC50值为 4.2 μM。它 对MMP-13、MMP-9MMP-8也具有抑制活性,IC50值分别为 12、23.3 和 25 μM。
T41179 CL 82198 hydrochloride

CL 82198 hydrochloride is a selective inhibitor of MMP-13 (89% inhibition at 10μg/mL) that displays no activity at MMP-1, MMP-9 or TACE. Inhibitsin vitroinvasion by the human pituitary adenoma cell line HP75. Rescues paclitaxel induced axon degradation and reduces associated neurotoxicity in zebrafish.
T72719 Tubulin/MMP-IN-2

Tubulin/MMP-IN-2是一种针对微管蛋白和基质金属蛋白酶的双重抑制剂,能有效抑制微管蛋白聚合并触发细胞凋亡。该化合物对MMP-2、MMP-3及MMP-9展现出明显的抑制效果,其IC50值分别为24.95 μM、31.60 μM与22.37 μM。Tubulin/MMP-IN-2主要应用于癌症研究领域。

化合物

MMP-2/MMP-9 Inhibitor I
Cat.No: T21512
Synonym:
Target: MMP
MMP-9-IN-1
Cat.No: T8310
Synonym:
Target: MMP
MMP-9-IN-6
Cat.No: T77617
Synonym:
Target: MMP
BPHA
Cat.No: T36712
Synonym: MMP-2/MMP-9 Inhibitor II
Target: MMP
MMP-9 Inhibitor I
Cat.No: T37726
Synonym:
Target:
MMP-9/MMP-13 Inhibitor I
Cat.No: T37172
Synonym:
Target:
SB-3CT
Cat.No: T2009
Synonym:
Target: MMP
MMP-9-IN-7
Cat.No: T72069
Synonym:
Target:
SM-7368
Cat.No: T22115
Synonym:
Target: NF-κB
NFAT Inhibitor
Cat.No: TP1015
Synonym: VIVIT peptide
Target: Others
MMP-9-IN-5
Cat.No: T64083
Synonym:
Target:
MMP-9-IN-3
Cat.No: T63155
Synonym:
Target:
MMP-9-IN-4
Cat.No: T63994
Synonym:
Target:
MMP-9-IN-8
Cat.No: T81777
Synonym:
Target:
MMP-2/9-IN-1
Cat.No: T62555
Synonym:
Target:
Marimastat
Cat.No: T6885
Synonym: BB2516,马立马司他,KB-R8898,TA2516
Target: MMP
S 3304
Cat.No: T16966
Synonym:
Target: MMP
Histatin 5 acetate
Cat.No: TP1741L
Synonym: Histatin 5 acetate (115966-68-2 Free base)
Target: MMP
JNJ0966
Cat.No: T4783
Synonym:
Target: MMP
MMP2-IN-3
Cat.No: T61271
Synonym:
Target: MMP
ARP-100
Cat.No: T14322
Synonym: MMP-2 Inhibitor III
Target: MMP
CTTHWGFTLC, CYCLIC acetate(244082-19-7 free base)
Cat.No: TP1501L
Synonym:
Target: MMP
Ilomastat
Cat.No: T2743
Synonym: Galardin,GM6001,伊洛马司他
Target: MMP
Batimastat
Cat.No: T6011
Synonym: 巴马司他,BB94
Target: MMP
Edaravone
Cat.No: T0407
Synonym: 依达拉奉右莰醇,依达拉奉,MCI-186
Target: Apoptosis, MMP, Free radical scavengers
Histatin 5 (TFA)(115966-68-2,free)
Cat.No: TP1446
Synonym: Histatin 5 (TFA)
Target: MMP
Batimastat sodium salt
Cat.No: T10461
Synonym: BB-94 sodium salt
Target: MMP
VPLSLYSG
Cat.No: T76618
Synonym:
Target:
ND-378
Cat.No: T28147
Synonym:
Target:
XL-784
Cat.No: T13358
Synonym:
Target: MMP
Prinomastat hydrochloride
Cat.No: T12539
Synonym: KB-R9896 hydrochloride,AG3340 hydrochloride
Target: MMP
GM 1489
Cat.No: T37983
Synonym:
Target:
Dnp-PLGMWSR (trifluoroacetate salt)
Cat.No: T36362
Synonym:
Target:
Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2
Cat.No: T36360
Synonym: Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2
Target:
MMI-166
Cat.No: T70051
Synonym:
Target:
CTTHWGFTLC, CYCLIC TFA
Cat.No: T76017
Synonym:
Target:
Tanomastat
Cat.No: T16986
Synonym: BAY 12-9566
Target: MMP
SD-2590 HCl
Cat.No: T24775
Synonym: SD2590 HCl,SD-2590 Hydrochloride,SD2590 Hydrochloride,SD 2590 Hydrochloride
Target:
CP-471474
Cat.No: T22685
Synonym: CP 471474
Target: Others
XL-784 free base
Cat.No: T13357
Synonym:
Target: Others
Prinomastat
Cat.No: T12539L
Synonym: KB-R9896,普啉司他,AG3340
Target: MMP
Histatin 5 TFA
Cat.No: T75755
Synonym:
Target:
ND-336
Cat.No: T28146
Synonym: ND336,ND-336 hydrochloride,ND 336
Target:
p-DDAP
Cat.No: T25925
Synonym: pDDAP,p-Dodecylaminophenol
Target:
Dnp-PLGLWA-DArg-NH2 TFA
Cat.No: T76269
Synonym:
Target:
IVMT-Rx-3
Cat.No: T82022
Synonym:
Target: NF-κB
ProMMP-9 inhibitor-3c
Cat.No: T69875
Synonym:
Target:
MMP2-IN-2
Cat.No: T60551
Synonym:
Target:
CL 82198 hydrochloride
Cat.No: T41179
Synonym:
Target:
Tubulin/MMP-IN-2
Cat.No: T72719
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T5S1026 Apigenin-7-glucuronide

Apigenin 7-O-glucuronide,芹菜素-7-葡萄糖醛酸

MMP Proteases/Proteasome
Apigenin-7-glucuronide (Apigenin 7-O-glucuronide) 能够抑制基质金属蛋白酶的活性,其对 MMP-3 (IC50:12.87 μM),MMP-8 (IC50:22.39 μM),MMP-9 (IC50:17.52 μM),MMP-13 (IC50:0.27 μM)。
T6S0325 Glycitein

黄豆黄素,Glycetein

Apoptosis; Others Apoptosis; Others
Glycitein (Glycetein) 是一种大豆异黄酮,可研究抗氧化和细胞凋亡。
T7044 Norepinephrine

去甲肾上腺素,Levophed,Levonoradrenaline,Aktamin,Nor-Epirenan,Levonor,Arterenol

MMP; Endogenous Metabolite; Adrenergic Receptor; Autophagy Autophagy; GPCR/G Protein; Metabolism; Neuroscience; Proteases/Proteasome
Norepinephrine (Levophed) 是β1选择性的肾上腺素能受体激动剂,EC50值为 5.37 μM。它可上调鼻咽癌肿瘤细胞中血管内皮生长因子、基质金属蛋白酶MMP-2和MMP-9的表达。
T6S0444 Salvianolic acid A

丹酚酸 A,Dan Phenolic Acid A

MMP Proteases/Proteasome
Salvianolic acid A (Dan Phenolic Acid A) 能够提高抑制基质金属钛酶 9 和抗炎作用,进而保护血脑屏障。
T5S1262 Methylophiopogonanone A

Others Others
Methylophiopogonanone A 是从Ophiopogon japonicas 提取到的黄酮类化合物,具有抗炎和抗氧化的特性。它通过调节 MMP-9 和紧密连接蛋白的表达来减轻 BBB 破坏的能力,具有治疗脑 I/R 损伤的潜力。
T3850 Luteolin 7-O-glucuronide

Luteolin-7-glucuronide,木犀草素-7-O-葡萄糖醛酸苷

MMP Proteases/Proteasome
Luteolin 7-O-glucuronide (Luteolin-7-glucuronide) 是一种自由基清除剂,能够抑制基质金属蛋白酶的活性,其对 MMP-1,MMP-3,MMP-8,MMP-9MMP-13的IC50值分别为 17.63,7.99,11.42,12.85,0.03 μM。
T3729 Ethyl gallate

Nipagallin A,Phyllemblin,gallic acid ethyl ester,没食子酸乙酯

MMP; NF-κB; Akt; Antibacterial Cytoskeletal Signaling; Microbiology/Virology; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome
Ethyl gallate (gallic acid ethyl ester) 是一种非类黄酮酚过氧化氢清除剂。
T5740 25(R,S)-Ruscogenin

(25RS)鲁斯可皂苷元,(25RS)-Ruscogenin

Others; HIF Angiogenesis; Chromatin/Epigenetic; Others
25(R,S)-Ruscogenin 能够调节 PI3K/Akt/mTOR 信号通路,抑制 MMP-2、MMP-9、uPA、VEGF 和 HIF-1α 的表达,阻碍肝癌转移。 它能够抑制 TLR4信号通路,减轻 LPS 诱导的肺内皮细胞凋亡。
T2973 Astragaloside IV

AST-IV,黄芪甲苷IV,AS-IV,黄芪皂苷 IV

MMP; ERK; Estrogen/progestogen Receptor; JNK Endocrinology/Hormones; MAPK; Proteases/Proteasome
Astragaloside IV (AS-IV) 是从黄芪中分离得到的一种皂苷,抑制ERK1/2和JNK 激活,在乳腺癌细胞 MDA-MB-231 中,下调(MMP)-2和(MMP)-9的信号通路。
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。
T5S2059 Glaucine

Calcium Channel; Dopamine Receptor; Influenza Virus; Adrenergic Receptor; PDE GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience
Glaucine 是从海罂粟中分离的一种生物碱,具有镇咳、抗炎和支气管扩张作用。它是具有口服活性的磷酸二酯酶 4 选择性抑制剂。它还是非选择性的 α-肾上腺素受体拮抗剂,具有抗氧化和抗病毒活性。
T3S1641 Esculentoside H

TNF; NF-κB; JNK Apoptosis; MAPK; NF-κB
Esculentoside H 是一种皂苷,分离自多年生植物 Phytolacca esculent 的根提取物中,具有抗肿瘤作用。它的机制与 TNF 释放能力有关。它能够阻断 JNK1/2和 NF-κB 信号介导的基质金属蛋白酶-9 (MMP-9) 表达,抑制结肠癌细胞迁移。
T4034 Solamargine

Solamargin,δ-Solanigrine,澳洲茄边碱

Apoptosis; p38 MAPK; P-gp; STAT Apoptosis; JAK/STAT signaling; MAPK; Membrane transporter/Ion channel; Neuroscience; Stem Cells
Solamargine (δ-Solanigrine) 是一种来源于茄属植物的类固醇 Solasodine 的衍生物,诱导非选择性细胞毒性和 P-gp 抑制作用。它通过下调 MMP-2 和 MMP-9 的表达和活性来显著抑制 HepG2 细胞的迁移和侵袭,在多种癌症中均表现出抗癌活性。
TN1879 Lucideric acid A

Lucidenic acid A,赤芝酸A

MMP; p38 MAPK; JNK MAPK; Proteases/Proteasome
Lucideric acid A (Lucidenic acid A) 是分离自灵芝的天然产物,可抑制 PMA 诱导的MMP-9活性,具有抵抗肝癌细胞侵袭的作用。
T5S0053 Coptisine

黄连碱,Coptisin

Indoleamine 2,3-Dioxygenase (IDO) Metabolism
Coptisine (Coptisin) 是一种从黄连中分离到的生物碱,是非竞争性的IDO 抑制剂,Ki=为 5.8 μM,IC50=6.3 μM。
T6S1699 Shogaol

[6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol

Lipoxygenase; Autophagy Autophagy; Metabolism
6-Shogaol (6-Shogaol) 是从生姜中分离的一种天然产物,具有抗癌、抗炎和抗氧化的多种生物活性。
T72730 D-Isofloridoside

D-Isofloridoside 是多糖前体之一,具有清除自由基、抑制ROS 表达、抑制MMP-2和MMP-9的活性。
T14121 Actinonin

(-)-Actinonin

Aminopeptidase Metabolism
Actinonin ((-)-Actinonin) is a naturally occurring antibacterial agent produced by Actinomyces and a potent reversible peptide deformylase (PDF) inhibitor with a Ki of 0.28 nM, it also is an apoptosis inducer. Actinonin inhibits aminopeptidase M, aminopeptidase N and leucine aminopeptidase, it also inhibits MMP-1, MMP-3, MMP-8, MMP-9, and hmeprin α with Ki values of 300 nM, 1,700 nM, 190 nM, 330 nM, and 20 nM, respectively. Actinonin has antiproliferative and antitumor activities[1][2][3][4][5].
TN1881 Lucidenic acid C

赤芝酸 C,赤芝酸C

MMP Proteases/Proteasome
Lucidenic acid C has anti-invasive effect, it shows significant inhibitory effects on PMA-induced MMP-9 activity and invasion of HepG(2 )cells.
TN4046 Excisanin A

MMP; FAK; PARP; GSK-3; NF-κB; Wnt/beta-catenin; Akt; Caspase; PI3K; Prostaglandin Receptor; JNK Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; MAPK; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells; Tyrosine Kinase/Adaptors
ExcisaninA may be a potent inhibitor of AKT signaling pathway in tumor cells, it can inhibit invasion by suppressing MMP-2 and MMP-9 expression, it may be a potential anti-metastatic chemotherapeutic agent for the treatment of breast cancer. Excisanin A shows comparable inhibitory effects on the LPS-induced production of NO and PGE2, and activation of NF-kappaB without affecting cell viability.Excisanin A induces apoptosis in colon cancer cell line SW620 as determined by Annexin V staining, the ...
TN1998 Notoginsenoside T5

三七皂苷T5

MMP Proteases/Proteasome
Total panax notoginsenosides (TPNS) are the main active ingredients in San-Chi, the root of(Burk) F.H. Chen, which belongs to the Araliaceae family and has been used in traditional Chinese medicine to treat atherosclerosis;TPNS can prevent atherosclerosis

天然产物

Apigenin-7-glucuronide
Cat.No: T5S1026
Synonym: Apigenin 7-O-glucuronide,芹菜素-7-葡萄糖醛酸
Target: MMP
Glycitein
Cat.No: T6S0325
Synonym: 黄豆黄素,Glycetein
Target: Apoptosis, Others
Norepinephrine
Cat.No: T7044
Synonym: 去甲肾上腺素,Levophed,Levonoradrenaline,Aktamin,Nor-Epirenan,Levonor,Arterenol
Target: MMP, Endogenous Metabolite, Adrenergic Receptor, Autophagy
Salvianolic acid A
Cat.No: T6S0444
Synonym: 丹酚酸 A,Dan Phenolic Acid A
Target: MMP
Methylophiopogonanone A
Cat.No: T5S1262
Synonym:
Target: Others
Luteolin 7-O-glucuronide
Cat.No: T3850
Synonym: Luteolin-7-glucuronide,木犀草素-7-O-葡萄糖醛酸苷
Target: MMP
Ethyl gallate
Cat.No: T3729
Synonym: Nipagallin A,Phyllemblin,gallic acid ethyl ester,没食子酸乙酯
Target: MMP, NF-κB, Akt, Antibacterial
25(R,S)-Ruscogenin
Cat.No: T5740
Synonym: (25RS)鲁斯可皂苷元,(25RS)-Ruscogenin
Target: Others, HIF
Astragaloside IV
Cat.No: T2973
Synonym: AST-IV,黄芪甲苷IV,AS-IV,黄芪皂苷 IV
Target: MMP, ERK, Estrogen/progestogen Receptor, JNK
Hinokiflavone
Cat.No: T4S0181
Synonym: 日本扁柏黄酮,扁柏双黄酮
Target: MMP, BCL, E1/E2/E3 Enzyme
Glaucine
Cat.No: T5S2059
Synonym:
Target: Calcium Channel, Dopamine Receptor, Influenza Virus, Adrenergic Receptor, PDE
Esculentoside H
Cat.No: T3S1641
Synonym:
Target: TNF, NF-κB, JNK
Solamargine
Cat.No: T4034
Synonym: Solamargin,δ-Solanigrine,澳洲茄边碱
Target: Apoptosis, p38 MAPK, P-gp, STAT
Lucideric acid A
Cat.No: TN1879
Synonym: Lucidenic acid A,赤芝酸A
Target: MMP, p38 MAPK, JNK
Coptisine
Cat.No: T5S0053
Synonym: 黄连碱,Coptisin
Target: Indoleamine 2,3-Dioxygenase (IDO)
Shogaol
Cat.No: T6S1699
Synonym: [6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol
Target: Lipoxygenase, Autophagy
D-Isofloridoside
Cat.No: T72730
Synonym:
Target:
Actinonin
Cat.No: T14121
Synonym: (-)-Actinonin
Target: Aminopeptidase
Lucidenic acid C
Cat.No: TN1881
Synonym: 赤芝酸 C,赤芝酸C
Target: MMP
Excisanin A
Cat.No: TN4046
Synonym:
Target: MMP, FAK, PARP, GSK-3, NF-κB, Wnt/beta-catenin, Akt, Caspase, PI3K, Prostaglandin Receptor, JNK
Notoginsenoside T5
Cat.No: TN1998
Synonym: 三七皂苷T5
Target: MMP
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