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PDF下载 Protease Inhibitors 蛋白酶抑制剂
单组分蛋白酶抑制剂 Single component Protease Inhibitors
|
Cat.No.
|
Product
|
M.W.
|
De
|
Solubility Stability
|
ConcentrationRangea)
|
Size
|
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12745.02
12745.03
|
AEBSF-HCl
[30827-99-7]
|
239.7
|
Irreversible inhibitor of Thrombin and other serine proteases. Inhibits by acylation of the active site of the enzyme. Much less toxic than PMSF and DFP.
凝血酶及其他丝氨酸蛋白酶的不可逆抑制剂，将活性位点酰基化。比PMSF 和DFP毒性小得多。
|
H2O,Aqueous solutions are stable between pH 5-6
|
0.1 - 2 µM
|
500mg
1g
|
|
12309.01
|
Amastatin-HCl
[100938-10-1]
|
511
|
Non-toxic reversible metallo -protease inhibitor. Inhibits many membrane-bound peptidases which are critical regulators of peptide hormones, e.g. aminopeptidase A and M, but not aminopeptidase B. Inhibits also leucine minopeptidase
金属蛋白酶可逆的抑制剂，无毒。可抑制许多肽激素类的膜结合肽，如氨基肽酶A和M（但不包括氨基肽酶B），也抑制亮氨酸氨基肽酶。
|
Ethanol
0.5 % AcOH |
1 - 100 µM
|
1mg
|
|
12548.03
|
ε-Aminocaproic acid
[60-32-2]
|
131.2
|
Highly active inhibitor of fibrinolysin and chymotrypsin.
溶纤维蛋白酶和胰凝乳蛋白酶的高活性抑制剂。
|
H2O
|
1 - 20 µM
|
100g
|
|
13684.01
|
α-Antichymot-ypsin from human plasma
[141176-92-3]
|
68000
|
Glycoprotein that inhibits chymotrypsin-like proteases (above all human neutrophil cathepsin G) by forming stable complexes. Acute phase protein; concentration in plasma increases after events like inflammation or tissue damage
通过形成稳定的复合物抑制胰凝乳蛋白酶类（包括所有嗜中性人组织蛋白酶G）的糖蛋白。急性时相蛋白；在发炎或组织损伤时在血浆中浓度会增加。
|
Aqueous buffers
|
Used at equimolar concentration
|
1mg
|
|
13685.01
13685.02
|
Antipain-HCL
[37682-72-7]
|
678.2
|
Reversible inhibitor of serine and cysteine proteases. Inhibits papain and trypsin more specificly than leupeptin. Plasmin is inhibited only slightly. Also involved in inhibition of RNA synthesis
丝氨酸和半胱氨酸蛋白酶可逆的抑制剂。比亮抑酶肽抑制木瓜蛋白酶和胰蛋白酶的专一性更高。
|
H2O
Methanol DMSO
|
1 - 100 µM
|
5mg
25mg
|
|
13695.01
|
Antithrombin III from human plasma
[90170-80-2]
|
ca. 60000
|
Glycoprotein that plays a major role in controlling serine proteases in the blood clotting cascade. Inactivates above all thrombin by forming an extremely stable complex, an effect which is enhanced by heparin. Inhibits also other proteases of the coagulation cascade like plasmin, kallikrein, factor IXa, Xa, XIa & XIIa.
主要在血液凝结中控制丝氨酸蛋白酶的糖蛋白。通过形成非常稳定的复合物抑制凝血酶的活性，可增强肝素钠的作用。也可抑制其他凝集类的蛋白酶，如纤维蛋白溶酶、激肽释放酶、IXa, Xa, XIa 和 XIIa因子。
|
H2O
|
Used at equimolar concentrations
|
1mg
|
|
13694.01
|
α1-Antitrypsin from human plasma α1-proteinase inhibitor
[9041-92-3]
|
ca.
53000
|
Glycoprotein that is mainly involved in the control of neutrophil elastase activity. Inhibits also most of other mammalian serine proteases but at a lower rate. Blocks the action of target enzymes by binding nearly irreversibly to their active site.
主要控制嗜中性酯酶活性的糖蛋白。也抑制大多数其他哺乳动物丝氨酸蛋白酶但速率低。与附近目标酶的活性位点不可逆的结合。
|
H2O
Aqueous buffers |
Used at equimolar concentra tions
|
5mg
|
|
13718.01
13718.02
13718.03
|
Aprotinin (Trypsin inhibitor from bovine lung)
[9087-70-1]
|
ca.
6500
|
Basic single-chain polypeptide that inhibits numerous serine proteases by binding to the active site of the enzyme, form ing tight complexes. It inhibits above all plasmin, kallikrein, trypsin, chymotrypsin and urokinase but not carboxypeptidase A and B, papain, pepsin, subtilisin, thrombin and factor X. Used in cell culture to prevent proteolytic damage to cells and to extend lifetime of cells.
基本的单链多肽，通过与酶的活性位点紧密结合形成复合物，抑制大多数的丝氨酸蛋白酶。抑制所有的纤维蛋白溶酶、激肽释放酶、胰蛋白酶、胰凝乳蛋白酶和尿激酶，但不包括羧肽酶A和B、木瓜蛋白酶、胃蛋白酶、枯草菌蛋白酶、凝血酶和X因子。用于细胞培养中防止细胞蛋白的水解并延长细胞寿命。
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H2O,Aqueous buffers. Sterile iltered solutions at pH 5-8 are stable for several months. Denatures at pH > 12
|
In cell culture: 0.01 - 3 µg/mL; in other applications: 10 - 250 µg/mL
|
10mg
25mg
100mg
|
|
13985.01
|
Arphamenine A
[144110-37-2]
|
387.4
|
Inhibitor of the metallo-protease Aminopeptidase B
金属蛋白酶氨基肽酶B的抑制剂
|
H2O, MeOH
|
IC50:
0.006 µg/mL |
5mg
|
|
13986.01
|
Arphamenine B
[144110-38-3]
|
403.4
|
Inhibitor of the metallo-protease Aminopeptidase B
金属蛋白酶氨基肽酶B的抑制剂
|
H2O, MeOH
|
IC50:
0.002 µg/mL |
5mg
|
|
14525.01
14525.02
|
Benzamidine-HCl
[1670-14-0]
|
174.6
|
Potent inhibitor of thrombin and trypsin
凝血酶和胰蛋白酶有效的抑制剂
|
H2O
|
0.1 - 50 µM
|
5g
25g
|
|
14980.02
|
Bestatin-HCl
[65391-42-6]
|
344.8
|
Metalloprotease inhibitor with multi-pharmacological functions. Inhibits cell surface aminopeptidases (notably B) and leucine aminopeptidase. Inhibitor of leukotriene A4 hydrolase and of enkephalin degradation in cell preparations from brain. Has anticarcinogenic and immunomodulating properties.
多种药理学功能的金属蛋白酶抑制剂。抑制细胞表面氨基肽酶（特别是B）和亮氨酸氨基肽酶。白三烯A4水解酶和脑细胞降解产生的脑啡肽的抑制剂。有抗癌和免疫调节功能。
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Methanol
(5 mg/mL) |
1 - 150 µM
Mitogenic effects at nmolar concentrations |
5mg
|
|
15520.02
|
CA-074
N/A
|
383.4
|
Inhibitor of Cathepsin B
组织蛋白酶B的抑制剂
|
DMSO
|
0.01 - 1 µM
|
5mg
|
|
15521.02
|
CA-074-Me
N/A
|
397.5
|
Proinhibitor for intracellular Cathepsin B. Membrane-permeable analog of CA-074
细胞内组织蛋白酶B的抑制剂前体。与CA-074膜渗透性类似。
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DMSO
|
1 µM
|
5mg
|
|
15700.01
|
Calpain Inhibitor I
[11004-82-1]
|
367.2
|
Tripeptide aldehyde. Specific inhibitor of the Ca2+-dependent cysteine protease calpain I and of cathepsin B and L.
三肽醛。Ca2+依赖性半胱氨酸蛋白酶钙蛋白酶I和组织蛋白酶B 和 L专属抑制剂
|
Ethanol,
Methanol, DMF, DMSO (10mg/mL) |
1 - 50 µM
|
25mg
|
|
15710.01
|
Calpain Inhibitor II
[136632-32-1]
|
385.2
|
Tripeptide aldehyde. Specific inhibitor of the Ca2+-dependent cysteine protease calpain II and of cathepsin B and L.
三肽醛。Ca2+依赖性半胱氨酸蛋白酶钙蛋白酶II和组织蛋白酶B 和 L专属抑制剂
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Ethanol, Methanol, DMF, DMSO(10 mg/mL)
|
1 -50 µM
|
25mg
|
|
52150.01
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Cathepsin Inhibitor Z-Phe-Gly-NHO- Bz-pMe
N/A
|
489.5
|
Specific inhibitor of Cathepsin B/L/S and Papain
组织蛋白酶B/L/S和木瓜蛋白酶的专属抑制剂
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DMSO, EtOH, Acetonitrile
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Ki:
0.15 - 16 µM |
1mg
|
|
17158.01
17158.02
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Chymostatin
[9076-44-2]
|
ca.
600
|
Peptide-derived aldehyde (mixture of 3 components). Reversible inhibitor of chymotrypsin-like serine and some cysteine proteases
肽醛（含三种组分）。胰凝乳蛋白酶类丝氨酸和某些半胱氨酸蛋白酶可逆的抑制剂。
|
DMSO
Acetic acid |
10 - 100 µM
|
5mg
25mg
|
|
77205.01
|
DFP
(Diisopropylfluoro phosphate)
[55-91-4]
|
184.2
|
A potent irreversible inhibitor of serine proteases and acetyl choline esterase. Highly toxic!
丝氨酸蛋白酶和乙酰胆碱酯酶高效的不可逆抑制剂。剧毒！
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Isopropanol; aqueous solutions are unstable
|
10 - 100 µM
|
1g
|
|
20600.01
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Diprotin A
[90614-48-5]
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341.5
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Reversible inhibitor of the metallo-protease Dipeptidylaminopeptidase IV
金属蛋白酶二肽氨基肽酶IV的可逆抑制剂
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H2O
|
Ki:2.2 µM
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50mg
|
|
21100.01
21100.02
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E-64
[66701-25-5]
|
357.4
|
Non-competitive irreversible inhibitor of papain and other cysteine proteases. Forms a thioether bond with the sulfhydryl group in the active center of the enzyme. Useful for active site titration: one mole of E-64 inhibits one mole of protease.
木瓜蛋白酶和其他半胱氨酸蛋白酶非竞争性不可逆的抑制剂。与酶活性中心的巯基形成硫醚键。用于活性位点的滴定：1mol的E-64抑制1mol的蛋白酶。
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H2O, DMSO Mixtures of water and ethanol
|
1 - 10 µM
|
5mg
25mg
|
|
21102.01
21102.02
|
E-64d (EST)
[88321-09-9]
|
342.4
|
Membrane-permeable analog of E-64c
与E-64c膜渗透性类似
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DMSO
|
1 µM
|
1mg
5mg
|
|
21000.01
21000.02
|
Ebelactone A
[76808-16-7]
|
338.5
|
Non-toxic inhibitor for esterases, acylpeptide hydrolase, lipase and N-formylmethionine aminopeptidase.
酯酶、酰基肽水解酶、脂肪酶和N-甲酰甲硫氨酸氨基肽酶无毒的抑制剂
|
Methanol
(200 mg/mL)
|
1 - 10 µM
|
1mg
5mg
|
|
21001.01
21001.02
|
Ebelactone B
[76808-15-6]
|
352.5
|
Non-toxic inhibitor for esterase, lipase and N-formyl-methionine aminopeptidase. Inhibits also carboxypeptidase Y-like exopeptidase.
酯酶、脂肪酶和N-甲酰甲硫氨酸氨基肽酶无毒的抑制剂。也抑制羧肽酶Y类外肽酶。
|
Methanol
(200 mg/mL)
|
1 - 10 µM
|
1mg
5mg
|
|
11280.01
11280.02
11280.03
|
EDTA-Na2
[6381-92-6]
|
372.3
|
Reversible inhibitor of metalloproteases
金属蛋白酶的可逆抑制剂
|
H2O (pH 8)
|
1 - 10 µM
|
100g
1kg
5kg
|
|
11290.01
11290.02
|
EGTA
[67-42-5]
|
380.4
|
Inhibits metalloproteases.. Reveals high selectivity for Ca2+ over Mg2+ ions.
Ca2+ over Mg2+ ions.
抑制金属蛋白酶。对Ca2+ 的选择性高于 Mg2+。
|
NH4OH, NaOH
|
1 - 10 µM
|
5g
50g
|
|
20947.01
|
Elastatinal
[51798-45-9]
|
512.6
|
Inhibitor of Elastase
弹性蛋白酶的抑制剂
|
H2O, MeOH, DMSO
|
Ki: 0.21 µM
(with-Ac-Ala-Ala-Ala-OMe as substrate) |
5mg
|
|
27736.01
|
Leuhistin
[129085-76-3]
|
241.3
|
Inhibitor of Aminopeptidase M
氨基肽酶M的抑制剂
|
H2O, DMSO,
EtOH, MeOH |
IC50:
0.2 µg/ml |
5mg
|
|
51867.02
51867.03
|
Leupeptin-hemisulfate
[24365-47-7]
|
475.6
|
Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.
三肽醛。丝氨酸和半胱氨酸蛋白酶可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酸酯酶D和C的活化。
|
H2O Stable for sereval months when stored in aliquots at -20 °C
|
1 - 100 µM
|
10mg
50mg
|
|
28301.01
|
α2-Macroglo-bulin from human plamas
[95568-41-5]
|
725000
|
Glycoprotein composed of 4 identical subunits. Broad-range endoproteinase inhibitor. Inhibits by forming a »trap« around the enzyme allowing only small substrate molecules to enter and to be cleaved by the entrapped protease.
含4个相同亚单位的糖蛋白。主要的内蛋白酶抑制剂。由截留酶在酶周围形成一个只能通过小分子底物的缺口。
|
H2O Stable for several months when stored in aliquots at -20 °C
|
Used at equimolar concentrations
|
1mg
|
|
31682.01
31682.02
|
4-(2-Aminoethyl) -benzenesulfonyl fluoride hydrochloride PEFABLOC® SC
[30827-99-7]
|
239.5
|
Water-soluble and relativly non-toxic irreversible inhibitor ofthrombin and other serine proteases. Inhibits by acylation of the active site of the enzyme.
水溶性的无毒不可逆抑制剂，通过酶活性位点的酰基化抑制制凝血酶和其他丝氨酸蛋白酶。
|
H2O(20 g/100 ml) Stable for several months between pH 5 - 6; limited stability above pH 7.5
|
0.1 - 5 mM in cell culture:
0.1 - 0.25 µM |
100mg
500mg
|
|
52682.02
52682.03
52682.04
|
Pepstatin A
[26305-03-3]
|
685.9
|
Pentapeptide derivative. Reversible inhibitor of aspartic proteases, e.g. pepsin, cathepsin D, chymosin,rennin.
五肽的衍生物。可逆的抑制天冬氨酸蛋白酶，如胃蛋白酶、组织蛋白酶D、凝乳酶
|
Methanol
(1 mg/mL) DMSO |
1 - 10 µM
|
5mg
25mg
100mg
|
|
31985.01
|
Phebestin
N/A
|
441.5
|
Inhibitor of Aminopeptidase N.
氨基肽酶N的抑制剂
|
H2O, DMSO, MeOH
|
IC50:
0.18 µg/ml |
1mg
|
|
32395.02
32395.03
32395.04
|
PMSF
Phenylmethyl sulfonyl fluoride [329-98-6]
|
174.2
|
Irreversibly inhibits serine proteases by sulfonylation of the serine residue in the active site of the protease. Inhibits also papain (reversible by DTT treatment) and acetylcholin-esterase. Does not inhibit metallo-, aspartic- and most cysteine proteases.
通过蛋白酶活性位点丝氨酸残基的磺酰化，不可逆的抑制丝氨酸蛋白酶。也抑制木瓜蛋白酶（用DTT处理可逆）和乙酰胆碱酯酶。但不抑制金属蛋白酶、天冬氨酸蛋白酶和大多数半胱氨酸蛋白酶。
|
Isopropanol, ethanol, methanol. (100 - 200mM) Unstable in aqueous solution
|
0.1 - 1 µM
|
5g
25g
100g
|
|
32753.01
|
Phosphoramidon
[119942-99-3]
|
587.5
|
Specific inhibitor of thermolysin and neutral endopeptidase-24.11 (ANP Degradation Enzyme). Inhibits also the activity of Endothelin Converting Enzyme, collagenase and metallo-endoproteinases from many microorganisms. Does not inhibit serine, cysteine and aspartic proteases.
嗜热菌蛋白酶和中性内蛋白酶-24.11（ANP降解酶）的专属抑制剂。也抑制内源性内皮素转化酶、胶原酶和微生物来源的金属内蛋白酶活性。
|
H2O
(20 mg/mL) DMSO Methanol |
1 - 100 µM
|
5mg
|
|
17013.02
17013.03
17013.04
|
TLCK
(1-Chloro-3-tosylamido -7-amino-2-heptanone HCl) [4238-41-9]
|
369.3
|
Irreversibly inhibits trypsin but not chymotrypsin by alkylating the histidine residue in the active site of the enzyme. Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain. TLCK does not react with zymogens or in active protease-inhibitor complexes.
通过乙酰化酶活性位点剩余的组氨酸，不可逆的抑制胰蛋白酶（但不含胰凝乳蛋白酶）。也抑制其他的丝氨酸和半胱氨酸蛋白酶，如菠萝蛋白酶、无花果蛋白酶和木瓜蛋白酶。不与酶原或活性蛋白酶抑制剂复合物反应。
|
1 mM HCl, DMSO H2O
(20mg/mL). Aqueous solutions are unstable above pH 7 |
10 - 1000 µM
|
100mg
250mg
1g
|
|
17016.02
17016.03
|
TPCK
(1-Chloro-3-tosylamido-4-phenyl-2-butanone) [402-71-1]
|
351.8
|
Irreversibly inhibits chymotrypsin but not trypsin by specifically reacting with histidine. Inhibits also other serine and cysteine protease such as bromelain, ficin and papain.
通过与组氨酸专一性反应，不可逆的抑制胰凝乳蛋白酶（但不含胰蛋白酶）。也抑制其他的丝氨酸和半胱氨酸蛋白酶，如菠萝蛋白酶、无花果蛋白酶和木瓜蛋白酶。
|
Ethanol (20 mg/mL) sparingly soluble in water; unstable at alkaline pH
|
10 - 1000 µM
|
250mg
1g
|
|
37310.03
|
Trypsin inhibitor from egg white
(Ovomucoid) 9035-81-8
|
ca. 28000
|
Monomeric Glycoprotein. Inhibits bovine (but not human) trypsin in a 1:1 molar ratio. Inhibition is reversible and pH dependant.
单体糖蛋白，1：1的浓度可逆的抑制牛（非人）胰蛋白酶，并与pH有关。
|
H2O,1mM HCl(1mg/mL) Very stable between pH 3 - 7 against heat and 9 M urea. Unstable at alkaline pH
|
Used at equimolar concentrations
(10-100 µg/ml) |
100mg
|
|
37328.01
|
Trypsin inhibitor from soybean
9035-81-8
|
ca. 22000
|
Monomeric protein. Reversible serine protease inhibitor. Inhibits trypsin, factor Xa, plasmin and plasma kallikrein, but not tissue kallikrein.
单体蛋白，丝氨酸蛋白酶的可逆抑制剂。抑制胰蛋白酶、因子Xa、血纤维蛋白溶解酶和血浆激肽释放酶（非组织激肽释放酶）
|
H2O(1mg/mL) Sensitive to heat and high pH
|
Used at equimolar concentrations (10-100 µg/ml)
|
50mg
|
混合蛋白酶抑制剂 Protease Inhibitor Mixes
- Protease Inhibitor Mix G
- 含5种成份的水溶性蛋白酶抑制剂，广泛的应用于半光氨酸、丝氨酸和金属蛋白酶的抑制，除常规使用还可用于需避免有机溶剂的环境。
- Protease Inhibitor Mix M
- 含6种成份，广泛用于天冬氨酸、半光氨酸和丝氨酸蛋白酶及氨基肽酶肽酶（金属蛋白酶）活性的抑制。特别适用于哺乳动物组织提取。
- Protease Inhibitor Mix P
- 含6种成份，广泛用于天冬氨酸、半光氨酸和丝氨酸蛋白酶、氨基肽酶肽酶及金属蛋白酶活性的抑制。特别适用于植物组织提取。
- Protease Inhibitor Mix FY
- 含4种成份，广泛用于天冬氨酸、半光氨酸和丝氨酸蛋白酶金属蛋白酶活性的抑制，特别适用于真菌及酵母提取物，可防止蛋白水解。
- Protease Inhibitor Mix B
- 含5种成份，广泛用于天冬氨酸、半光氨酸和丝氨酸蛋白酶、氨基肽酶肽酶及金属蛋白酶活性的抑制。特别适用于细菌提取物。
- Protease Inhibitor Mix HP
- 含4种成份的水溶性蛋白酶抑制剂，广泛适用于半光氨酸和丝氨酸蛋白酶的抑制，不含金属螯合物。推荐用于纯化聚组氨酸标记蛋白，以及其他需避免金属螯合剂的情况。
所有的蛋白酶抑制剂混合物均为冻干粉末，使稳定性提高，操作更简便，粉末可完全溶解。用1ml水或1ml 90% DMSO重新溶解后得到的溶液，足够用于100ml的细胞溶解物或蛋白溶液的处理。溶解的蛋白酶抑制剂混合物可分装，并在-20 °C储存4周以上。
|
Cat.No.
|
Product
|
Protease Inhibitor
|
Acting against
|
Size
|
|
39101.01
39101.02 39101.03 |
Protease Inhibitor Mix G
(general applications ; soluble in water)
|
AEBSF-HCl
Aprotinin from boving lung
E-64
EDTA-Disodium
Leupeptin
|
Serine proteases
Serine proteases
Cysteine proteases
Metallo proteases
Cysteine proteases & Trypsin-like Serine proteases
|
1 vial
5 vials 10 vials |
|
39102.01
39102.02 39102.03 |
Protease Inhibitor Mix M
(Mammalian cells; soluble in 90% DMSO,1 ml 90% DMSO per vial is included)
|
AEBSF-HCl
Aprotinin from boving lung
Bestain
E-64
Leupeptin
Pepstain A
|
Serine proteases
Serine proteases
Aminopeptidase B & Leucine Aminopetidase
Cysteine proteases
Cysteine proteases & Trypsin-like Serine proteases
Aspartic Protease
|
1 vial
5 vials 10 vials |
|
39103.01
39103.02 39103.03 |
Protease Inhibitor Mix P
(Plant cells; soluble in 90%DMSO, 1 ml 90% DMSO per vial is included)
|
AEBSF-HCl
E-64
Bestain
1,10-Phenanthroline
Pepstain A
Leupeptin
|
Serine proteases
Cysteine proteases
Aminopeptidase B & Leucine Aminopetidase
Metallo proteases
Aspartic Protease
Cysteine proteases & Trypsin-like Serine proteases
|
1 vial
5 vials 10 vials |
|
39104.01
39104.02 39104.03 |
Protease Inhibitor Mix FY
(Fungi and yeast cells; soluble in 90%DMSO, 1 ml 90% DMSO per vial is included)
|
AEBSF-HCl
E-64
Pepstain A
1,10-Phenanthroline
|
Serine proteases
Cysteine proteases
Aspartic Protease
Metallo proteases
|
1 vial
5 vials 10 vials |
|
39105.01
39105.02 39105.03 |
Protease Inhibitor Mix B
(Bacterial cells; soluble in 90%DMSO, 1 ml 90% DMSO per vial is included)
|
AEBSF-HCl
E-64
Pepstain A
EDTA-Disodium
Bestain
|
Serine proteases
Cysteine proteases
Aspartic Protease
Metallo proteases
Aminopeptidase B & Leucine Aminopetidase
|
1 vial
5 vials 10 vials |
|
39106.01
39106.02 39106.03 |
Protease Inhibitor Mix HP
(Recombinant proteins; soluble in water)
|
AEBSF-HCl
Aprotinin from boving lung
E-64
Leupeptin
|
Serine proteases
Serine proteases
Cysteine proteases
Cysteine proteases & Trypsin-like Serine proteases
|
1 vial
5 vials 10 vials |
Other Enzyme Inhibitors 其他酶抑制剂
|
Cat.No.
|
Product Name
|
CAS
|
Size
|
|
10017.01
10017.02
10017.03
|
Acarbose from Actinoplanes sp. ca. 100 FIP-AIU/mg contact dried amorph
|
56180-94-0
|
100mg
500mg
1g
|
|
16570.01
16570.02
|
Chelerythrine chloride research grade
|
3895-92-9
|
1mg
5mg
|
|
17700.01
|
Cyclopiazonic acid research grade
|
N/A
|
5mg
|
|
15160.01
|
Elastase Inhibitor I
|
N/A
|
1mg
|
|
22177.01
|
Genistein research grade
|
446-72-0
|
25mg
|
|
26020.01
|
Hypericin research grade
|
548-04-9
|
1mg
|
|
27750.02
|
Levamisole.HCl analytical grade
|
16595-80-5
|
5g
|
|
32010.01
32010.02
|
1,10-Phenanthroline analytical grade
|
66-71-7
|
5g
25g
|
|
33767.01
33767.02
|
Proteasome Inhibitor MG-115
|
N/A
|
1mg
5mg
|
|
33766.01
33766.02
|
Proteasome Inhibitor MG-132
|
N/A
|
1mg
5mg
|
|
33765.01
33765.02
|
Proteasome Inhibitor PSI
|
N/A
|
1mg
5mg
|
|
26856.01
|
Protein Kinase Inhibitor K-252a research grade
|
97161-97-2
|
0.1mg
|
|
26865.01
|
Protein Kinase Inhibitor K-252b research grade
|
99570-78-2
|
0.1mg
|
|
26873.01
|
Protein Kinase Inhibitor KT 5720 research grade
|
108068-98-0
|
0.1mg
|
|
26874.01
|
Protein Kinase Inhibitor KT 5823 research grade
|
126643-37-6
|
0.1mg
|
|
35385.01
35385.02
|
Staurosporine research grade
|
62996-74-1
|
0.1mg
0.5mg
|
|
36000.01
|
Thapsigargin research grade
|
67526-95-8
|
1mg
|
|
38385.01
38385.02
38385.03
|
Wortmannin from Penicillium fumiculosum research grade
|
19545-26-7
|
1mg
5mg
10mg
|
