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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11615 |
IDO-IN-12
|
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-12 是吲哚胺 2,3-双加氧酶抑制剂。 | |||
T39598 |
4-Chlorocatechol
|
Others | Others |
4-Chlorocatechol, a significant degradation product of 4-chloro-2-aminophenol (4C2AP), serves as a substrate for both catechol 1,2-dioxygenases and chlorocatechol dioxygenase [1] [2]. | |||
T11901 |
IDO1-IN-5
|
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO1-IN-5 是可透过血脑屏障的、选择性的IDO1抑制剂,能够与缺乏血红素的 apo-IDO1 结合,但无法与成熟血红素的 IDO1 结合。 | |||
T11616 |
IDO-IN-13
GS-4361 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-13 (GS-4361) 是 indoleamine 2,3-dioxygenase 1 抑制剂,EC50=17 nM。 | |||
T10199 |
GNF-PF-3777
8-Nitrotryptanthrin |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
GNF-PF-3777 (8-Nitrotryptanthrin) 是人吲哚胺2,3-双加氧酶 2 (hIDO2) 抑制剂,能够降低IDO2活性,Ki=为 0.97 μM。 | |||
T9164 |
BMS-986242
BMS986242 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
BMS-986242 是具有口服具有活力、强效的、选择性的 indoleamine-2,3-dioxygenase 1 抑制剂,可用于研究癌症。 | |||
T2647 |
IDO5L
INCB024360 analogue,INCB14943 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO5L (INCB024360 analogue) 是一种有效的吲哚胺-2,3-双加氧酶 (IDO) 抑制剂,IC50=67 nM。 | |||
T4532 |
Linrodostat
BMS-986205 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Linrodostat (BMS-986205) 是选择性的、不可逆的吲哚胺 2,3-双加氧酶 1(IDO1) 抑制剂,能够有效抑制 IDO1-HEK293 细胞,其IC50=1.1 nM。它在晚期癌症中具有良好的药理特性。 | |||
T4307 |
PF-06840003
EOS200271,PF 06840003 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
PF-06840003 (EOS200271) 是口服具有活力的、选择性的IDO-1抑制剂,抑制 hIDO-1, dIDO-1和 mIDO-1 的IC50分别为 0.41 μM, 0.59 μM,和 1.5 μM。 | |||
TQ0071 |
Navoximod
GDC-0919,NLG-919 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Navoximod (GDC-0919) 是 IDO(indoleamine-(2,3)-dioxygenase) 抑制剂,Ki=7 nM/,EC50=75 nM。 | |||
T3548 |
Epacadostat
INCB 024360,艾卡哚司他,IDO Inhibitor 1 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Epacadostat (INCB 024360) 是选择性的IDO1抑制剂,IC50=71.8 nM。 | |||
T7181 |
IDO-IN-1
4-氨基-N-(3-溴-4-氟苯基)-N'-羟基-1,2,5-恶二唑-3-甲脒 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-1 是吲哚胺-2,3-双加氧酶抑制剂,IC50=59 nM。 | |||
T1847 |
Necrostatin-1
Nec-1,Necrostatin 1 |
Indoleamine 2,3-Dioxygenase (IDO); Ferroptosis; Autophagy; RIP kinase | Apoptosis; Autophagy; Metabolism; NF-κB |
Necrostatin-1 (Nec-1) 是一种坏死性凋亡抑制剂和 RIP1 抑制剂,具有特异性。Necrostatin-1 抑制 TNF-α 诱导的坏死性凋亡。Necrostatin-1 也可以抑制 IDO。 | |||
T1806 |
IDO-IN-7
NLG919,Navoximod,NLG-919 analogue,GDC-0919 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-7 (NLG-919 analogue) 是 IDO1 抑制剂,IC50=38 nM。 | |||
T4142 |
PCC0208009
IDO inhibitor 1,DO-IN-2,IDO-IN-2 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
PCC0208009 (IDO-IN-2) 是一种有效的 IDO 抑制剂,其在 HeLa 细胞中的 IC50=4.52 nM。它调节 ACC 和杏仁核的突触可塑性,减少神经性疼痛和合并症。 | |||
T6543 |
Indoximod
NLG-8189,Indoximod (NLG-8189),1-Methyl-D-tryptophan,吲哚莫德 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Indoximod (Indoximod (NLG-8189)) 是一种具有口服具有活力的吲哚胺2,3-双加氧酶(IDO) 途径抑制剂。它在调节 mTOR 中充当 Trp 模拟物。它是一种可用于癌症研究的免疫代谢佐剂。 | |||
T40421 |
4,5-Dichlorocatechol
|
Others | Others |
4,5-Dichlorocatechol 是广谱的pseudomonas chlororaphisRW71 氯邻苯二酚 1,2-二加氧酶的底物。对于Pseudomonas putidaAC27 菌株双加氧酶和AcidovoraxPS14 菌株双加氧酶的Ki 都为 30 nM。 | |||
T1684 |
Nitisinone
尼替西农,NTBC,SC0735,Nitisone |
Others; Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB; Others |
Nitisinone (SC0735) 是一种 4-羟基苯丙酮酸双加氧酶抑制剂。 | |||
T20513 |
IDO1-IN-1
IDO1 inhibitor 1,2 HzBTZ,2-肼基苯并噻唑,IDO1IN1,2-HzBTZ,IDO1-inhibitor-1 |
IDO | Metabolism |
IDO1-IN-1 (2 HzBTZ) 是一种吲哚胺 2,3-双加氧酶 1 (IDO1) 抑制剂。 | |||
T7660 |
IDO inhibitor 1
4-[[2-[(氨基磺酰基)氨基]乙基]氨基]-N'-(3-溴-4-氟苯基)-N-羟基-1,2,5-恶二唑-3-甲脒 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO inhibitor 1 是一种有效的吲哚胺-2,3 双加氧酶 (IDO) 抑制剂 (IC50 <100 nM)。具有潜在的免疫调节和抗肿瘤活性。 | |||
T16951 |
Sulcotrione
|
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Sulcotrione 属于β-三酮类除草剂,对羟基苯基丙酮酸双加氧酶有抑制作用。 | |||
T39476 |
NLG802
|
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
NLG802 是 indoximod 的前药,indoximod 是一种口服活性的吲哚胺2,3-双加氧酶(IDO)抑制剂。 | |||
T20318 |
Benzylideneaniline
N-苄叉苯胺,N-Benzylideneaniline |
Others | Others |
Benzylideneaniline (N-Benzylideneaniline) 是一种有效的木质芪-α,β-双加氧酶抑制剂,它是氧化裂解木质芪中心双键的关键酶。 | |||
T36624L |
α-Hydroxyglutaric Acid Lithium
α-Hydroxyglutaric Acid Lithium(2889-31-8 Free base) |
Decarboxylase; Endogenous Metabolite; mTOR | Metabolism; Others; PI3K/Akt/mTOR signaling |
α-Hydroxyglutaric Acid Lithium 在微生物和动物体内有谷氨酸转化而来,是 α-酮戊二酸依赖性双加氧酶和 5-甲基胞嘧啶羟化酶抑制剂,对 ATP 合酶和 mTOR 信号传导有抑制作用。 | |||
T4410 |
LM10
|
Others | Others |
LM10 是有效的色氨酸 2,3-双加氧酶的抑制剂。色氨酸 2,3-双加氧酶是一种无关的肝酶,它可通过犬尿氨酸途径降解色氨酸。它对研究癌症疾病具有潜在的研究价值。 | |||
T61202 |
TDO-IN-1
|
Others | Others |
TDO-IN-1 是一种具有口服活性、有效性和选择性的色氨酸 2,3-双加氧酶 (TDO)抑制剂 ,对吲哚胺-2,3-双加氧酶 具有抑制作用。TDO-IN-1 具有抗肿瘤活性, 能够通过逆转肿瘤组织的局部免疫耐受来发挥作用。 | |||
T6820 |
D-α-Hydroxyglutaric acid disodium
D-alpha-Hydroxyglutaric acid disodium salt,(R)-2-羟基戊二酸二钠盐,Disodium (R)-2-Hydroxyglutarate |
ATPase; Others; Reactive Oxygen Species; Endogenous Metabolite; mTOR | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB; Others; PI3K/Akt/mTOR signaling |
D-α-Hydroxyglutaric acid disodium (Disodium (R)-2-Hydroxyglutarate) 是神经代谢疾病 D-2-羟基戊二酸尿症中积累的主要代谢产物,可增加活性氧的产生。它是 α-酮戊二酸 (α-KG) 的弱竞争拮抗剂,可抑制多种α-KG 依赖性双加氧酶,Ki 为 10.87 mM。 | |||
T11623 |
IDO/TDO-IN-1
|
Others | Others |
IDO/TDO-IN-1 is an orally active dual indoleamine-2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO) inhibitor (IC50s: 9.7 and 47 nM). | |||
T11618 |
IDO-IN-4
|
Others | Others |
IDO-IN-4 is an indoleamine 2,3-dioxygenase 1 (IDO-1) inhibitor. | |||
T11620 |
IDO-IN-6
NLG-1486 |
IDO | Metabolism |
IDO-IN-6 is an indoleamine 2,3-dioxygenase (IDO) inhibitor. | |||
T74992 |
NU223612
|
Others | Others |
NU223612 是一种有效的PROTAC(PROTACs),可降解吲哚胺 2,3-双加氧酶 1 (IDO1) (Indoleamine 2,3-Dioxygenase (IDO)),Kd 为 640 nM。NU223612 通过CRBN 介导的蛋白酶体降解有效降解IDO1蛋白。NU223612 以 290 nM 的亲和力与 CRBN 结合。NU223612 可以穿过血脑屏障 (BBB)。 | |||
T11619 |
IDO-IN-5
NLG-1489 |
IDO | Metabolism |
IDO-IN-5 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM). | |||
T11617 | IDO-IN-3 | IDO | Metabolism |
IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM). | |||
T11621 |
IDO-IN-8
NLG-1487 |
IDO | Metabolism |
IDO-IN-8 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM). | |||
T70189 |
Navoximod phosphate
|
Others | Others |
Navoximod phosphate is an indoleamine 2,3-dioxygenase (IDO) inhibitor, immunomodulator and antineoplastic. | |||
T11622 |
IDO-IN-9
|
IDO | Metabolism |
IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.011 μM (Kinase) and 0.0018 μM (Hela Cell). | |||
T40493 |
3,6-Dichlorocatechol
|
Others | Others |
3,6-Dichlorocatechol serves as a substrate for the broad-spectrum chlorocatechol 1,2-dioxygenase found in pseudomonas chlororaphis RW71. | |||
T40497 |
3,4-Dichlorocatechol
|
Others | Others |
3,4-Dichlorocatechol serves as a substrate for the broad-spectrum chlorocatechol 1,2-dioxygenase enzyme found in pseudomonas chlororaphis RW71. | |||
T11614 | IDO-IN-11 | IDO | Metabolism |
IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell). | |||
T38781 |
3,5-Dichlorocatechol
|
Others | Others |
3,5-Dichlorocatechol serves as a substrate for the broad-spectrum chlorocatechol 1,2-dioxygenase found in pseudomonas chlororaphis RW71. | |||
T14531 |
Benzobicyclon
|
Others | Others |
Benzobicyclon is a pro-herbicide and it acts as an inhibitor of 4-hydroxyphenylpyruvate dioxygenase (4-HPPD) in plant, and leads to bleaching and death[1]. | |||
T68792 |
Abamine
|
Others | Others |
Abamine is an inhibitor of 9-Cis-Epoxycarotenoid dioxygenase (NCED), the key regulatory enzyme in the plant hormone abscisic acid (ABA) biosynthesis pathway. | |||
T73437 |
DP00477
|
Others | Others |
DP00477,一种高效IDO1(indoleamine 2,3-dioxygenase 1)抑制剂,IC50为7.0 µM,展现在癌症研究中的潜力。 | |||
T60698 |
Roxyl-9
|
Others | Others |
Roxyl-9 是一种 IDO1 (吲哚胺2,3-双加氧酶1) 抑制剂。 | |||
T12668 |
(Rac)-IDO1-IN-5
|
Others | Others |
(Rac)-IDO1-IN-5 is a racemate of IDO1-IN-5, a potent, selective, and brain-penetrating inhibitor of Indoleamine 2,3-Dioxygenase 1 (IDO1) activity. It specifically binds to apo-IDO1, which lacks heme, instead of mature heme-bound IDO1. | |||
T37329 |
PROTAC IDO1 Degrader-1
PROTAC IDO1 Degrader-1 |
PROTACs | PROTAC |
PROTAC IDO1 Degrader-1 is the first potent IDO1 (indoleamine 2,3-dioxygenase 1) degrader that hijacks IDO1 to CRBN E3 ligase to introduce IDO1 into UPS and eventually achieve ubiquitination and degradation (DC50=2.84 μM). PROTAC IDO1 Degrader-1 moderately improves the tumor-killing activity of H ER2 CAR-T cells[1]. PROTAC IDO1 Degrader-1 (compound 2c) (10 μM; 24 hours) notably decreases IDO1 level induced by IFN-γ[1].PROTAC IDO1 Degrader-1 and IFN-γ (5 ng/mL) are incubated with HeLa cells for 24... | |||
T82082 |
IDO1-IN-23
|
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO1-IN-23(化合物41)是一种有效的人类IDO1抑制剂,具备13 μM的IC50值。 | |||
T39888 |
IDO1-IN-7
IDO1-IN-7 |
Others | Others |
IDO1-IN-7, a potent and selective indoleamine-2,3-dioxygenase-1 (IDO1) inhibitor, exhibits high potency with an IC 50 of 6.1 nM in the cellular assay (SKOV3). Apart from its inhibitory properties, IDO1-IN-7 also demonstrates immunomodulatory effects, contributing to its potential applications in cancer research. | |||
T60266 |
(Rac)-Indoximod
|
Others | Others |
(Rac)-Indoximod (1-Methyl-DL-tryptophan) is a potent inhibitor of indoleamine 2,3-dioxygenase (IDO). Combined treatment with IFN-γ and (Rac)-Indoximod significantly suppresses the activity of α-SMA-expressing human cardiac myofibroblasts (hCMs) and promotes apoptosis by up-regulating the genes IRF-1, Fas, and FasL. Moreover, this co-treatment effectively improves cardiac fibrosis[1]. | |||
T74369 |
Topramezone
|
Others | Others |
Topramezone为高效的4-羟基苯基丙酮酸双加氧酶(4-HPPD)抑制剂,作为除草剂(herbicide),适用于防治玉米中的阔叶杂草和禾本科杂草出苗后。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4S0051 |
Coptisine sulfate
|
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Coptisine Sulfate 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。 | |||
T3S1967 |
(S)-Indoximod
N-ME-Tryptophan,Abrine,相思豆碱,L-Abrine |
Others; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism; Others |
(S)-Indoximod (L-Abrine) 是一种吲哚胺-2,3-双加氧酶 (IDO) 抑制剂,可用于研究癌症。 | |||
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。 | |||
T2718 |
Palmatine chloride
|
Others; Indoleamine 2,3-Dioxygenase (IDO); Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Others |
Palmatine chloride 是口服具有活力的不可逆 IDO-1抑制剂。它能够减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,并改善 DSS 诱发的结肠炎。 | |||
T5S0056 |
Coptisine chloride
盐酸黄连碱,氯化黄连碱,Q-100696,NSC-119754 |
Indoleamine 2,3-Dioxygenase (IDO); Influenza Virus; Antibacterial | Metabolism; Microbiology/Virology |
Coptisine chloride (NSC-119754) 是从黄连中分离到的一种生物碱,是一种非竞争性 IDO 抑制剂,Ki 值为 5.8 μM,IC50值为 6.3 μM。它是一种 H1N1 神经氨酸酶抑制剂,可用于甲型流感病毒感染,IC50为 104.6 μg/mL。 | |||
T5S0802 |
Palmatine
巴马汀,Berbericinine,Burasaine |
Indoleamine 2,3-Dioxygenase (IDO); AChR; AChE; Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Neuroscience |
Palmatine (Burasaine) 是口服具有活力的、不可逆IDO-1抑制剂。它可以减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,从而改善DSS (Dextran Sulphate Sodium Salt) 诱发的结肠炎。它有用于结肠炎的研究潜力。 | |||
T8214 |
Kushenol E
苦参醇E,Flemiphilippinin D |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Kushenol E (Flemiphilippinin D) 是一种分离自Sophora flavescens 中的类黄酮,是一种IDO1的非竞争性抑制剂,其IC50=7.7 µM,Ki=为 9.5 µM,具有抗肿瘤特性。 | |||
T4779 |
4-Methylcatechol
p-Methylcatechol,3,4-二羟基甲苯,Homocatechol,4-methylbenzene-1,2-diol,3,4-Dihydroxytoluene |
Others; Endogenous Metabolite | Metabolism; Others |
4-Methylcatechol (3,4-Dihydroxytoluene) 是 p-toluate 的代谢物,它是 Catechol 2,3-Dioxygenase 的自杀性底物抑制剂。 | |||
T5066 |
Nε,Nε,Nε-Trimethyllysine chloride
Lys(Me)3-OH Chloride,Nε,Nε,Nε-Trimethyllysine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Nε,Nε,Nε-Trimethyllysine chloride (Lys(Me)3-OH Chloride) 是肠道菌群依赖性形成 N,N,N-trimethyl-5-aminovaleric acid (TMAVA) 的前体。 | |||
T4858 |
4-Hydroxyphenylpyruvic acid
4-羟苯基丙酮酸,4-Hydroxyphenylpyruvic acid |
Endogenous Metabolite | Metabolism |
4-Hydroxyphenylpyruvic acid 是一种苯丙氨酸代谢的中间产物,是一种酶抑制剂。 | |||
T72508 |
Palmatine hydroxide
|
Others | Others |
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。 | |||
T82822 |
Brassicanate A sulfoxide
|
||
Brassicanate A sulfoxide 表现出除草效果,它能抑制植物中必需氨基酸的生物合成路径。该化合物通过结合并抑制多种酶的活性来发挥其作用,包括二羟酸脱水酶 (DHAD)、羟甲基丙酮酸双加氧酶 (HPPD)、乙酰乳酸合酶 (ALS)、PYL家族蛋白及转运抑制剂响应 1 (TIR1)。Brassicanate A sulfoxide 可以从甘蓝 (Brassica oleracea) 中提取获得。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02928 |
IDO Protein, Human, Recombinant
IDO-1,Indoleamine 2,3‑dioxygenase,indoleamine 2,3-<... |
Human | E. coli |
IDO Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 45.2 kDa and the accession number is A0A348GSI3. | |||
TMPY-01821 |
IDO Protein, Human, Recombinant (His)
IDO,indoleamine 2,3-dioxygenase 1,Indoleamine 2,3‑<... |
Human | E. coli |
IDO Protein, Human, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 46 kDa and the accession number is P14902-1. | |||
TMPY-04176 |
HAAO Protein, Rat, Recombinant (His)
3-hydroxyanthranilate 3,4-dioxygenase |
Rat | E. coli |
HAAO Protein, Rat, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 34.8 kDa and the accession number is P46953. | |||
TMPY-02803 |
IDO2 Protein, Human, Recombinant (His)
indoleamine 2,3-dioxygenase 2,INDOL1 |
Human | E. coli |
IDO2 belongs to the indoleamine 2,3-dioxygenase family. Indoleamine 2,3-dioxgyenase (IDO), is a cytosolic haem protein which, together with the hepatic enzyme tryptophan 2,3-dioxygenase, catalyzes the conversion of tryptophan and other indole derivatives to kynurenines. In addition to classic IDO (IDO1), a new variant, IDO2, has recently been described. IDO2 is expressed in the liver, small intestine, spleen, placenta, thymus, lung, brain, kidney, and colon. IDO is widely distributed in human ti... | |||
TMPH-00047 |
DODA Protein, Amanita muscaria, Recombinant (His & Myc)
DOPA 4,5-dioxygenase,DODA |
Amanita muscaria | E. coli |
Extradiol dioxygenase that opens up the cyclic ring of DOPA between carbons 4 and 5 thus producing an unstable seco-DOPA that rearranges non-enzymatically to betalamic acid. Can also catalyze the formation of muscaflavin (a pigment found in the hygrocybe mushrooms family and of some amanita species only) by a 2,3-extradiol cleavage of DOPA. DODA Protein, Amanita muscaria, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight... | |||
TMPJ-01142 |
CDO1 Protein, Human, Recombinant (His)
CDO-I,CDO,Cysteine Dioxygenase Type I,CDO1,Cysteine... |
Human | E. coli |
Cysteine Dioxygenase Type 1 (CDO1) is a mammalian non-heme iron enzyme that belongs to the cysteine dioxygenase family. CDO1 is highly expressed in the liver and placenta, and has a low expression in heart, brain and pancreas. CDO1 can also be detected in hepatoblastoma HepG2 cells. CDO1 catalyzes the conversion of L-cysteine to cysteine sulfinic acid by incorporation of dioxygen. CDO1 is a vital regulator of cellular cysteine concentrations and has an essential role in maintaining the hepatic c... | |||
TMPY-06772 |
IDO Protein, Mouse, Recombinant (His)
Indo,indoleamine 2,3-dioxygenase 1,Ido |
Mouse | E. coli |
IDO Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 46.47 kDa and the accession number is P28776. | |||
TMPH-03159 |
DODA Protein, Portulaca grandiflora, Recombinant (His & Myc & SUMO)
DOPA 4,5-dioxygenase,DODA |
Portulaca grandiflora | E. coli |
Opens the cyclic ring of dihydroxy-phenylalanine (DOPA) between carbons 4 and 5, thus producing an unstable seco-DOPA that rearranges nonenzymatically to betalamic acid. DODA Protein, Portulaca grandiflora, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 49.9 kDa and the accession number is Q7XA48. | |||
TMPY-04909 |
HAAO Protein, Human, Recombinant (His & GST)
3-hydroxyanthranilate 3,4-dioxygenase,3-HAO,HAO |
Human | Baculovirus Insect Cells |
HAAO Protein, Human, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 60.4 kDa and the accession number is P46952-1. | |||
TMPH-03187 |
PHT3 Protein, Pseudomonas putida, Recombinant (His & Myc)
pht3,Phthalate 4,5-dioxygenase oxygenase subunit |
Pseudomonas putida | E. coli |
N/A. PHT3 Protein, Pseudomonas putida, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 56.7 kDa and the accession number is Q05183. | |||
TMPH-00025 |
DELTA-actitoxin-Aeq1a Protein, Acinetobacter baumannii, Recombinant (His & SUMO)
1,2-CTD,catA,Catechol 1,2-dioxygenase |
Acinetobacter baylyi | E. coli |
DELTA-actitoxin-Aeq1a Protein, Acinetobacter baumannii, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 50.3 kDa and the accession number is P07773. | |||
TMPH-03186 |
Metapyrocatechase Protein, Pseudomonas putida, Recombinant (His & Myc & SUMO)
Catechol 2,3-dioxygenase,xylE,CatO2ase,Metapyrocate... |
Pseudomonas putida | E. coli |
N/A. Metapyrocatechase Protein, Pseudomonas putida, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 55.2 kDa and the accession number is P06622. | |||
TMPY-03756 |
BBOX1 Protein, Human, Recombinant (His & GST)
butyrobetaine (γ), 2-oxoglutarate dioxygenase (γ-bu... |
Human | Baculovirus Insect Cells |
BBOX1, also known as gamma-BBH, belongs to thegamma-BBH/TMLD family. It is highly expressed in kidney and moderately expressed in liver. BBOX1 catalyzes the formation of L-carnitine from gamma-butyrobetaine, the last step in the L-carnitine biosynthetic pathway. Carnitine is essential for the transport of activated fatty acids across the mitochondrial membrane during mitochondrial beta-oxidation. BBOX1 is an inhibition target for mildronate which can be used to treatanginaandmyocardial infarctio... | |||
TMPH-00026 |
Catechol 1,2-dioxygenase Protein, Acinetobacter baylyi, Recombinant (His)
Equinatoxin-2,EqTII,DELTA-AITX-Aeq1a,Equinatoxin II,DELTA-ac... |
Actinia equina | E. coli |
Catechol 1,2-dioxygenase Protein, Acinetobacter baylyi, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 23.9 kDa and the accession number is P61914. | |||
TMPH-00577 |
AlkB Protein, E. coli, Recombinant (His & Myc & SUMO)
Alpha-ketoglutarate-dependent dioxygenase AlkB homo... |
E. coli | E. coli |
AlkB Protein, E. coli, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 44.1 kDa and the accession number is P05050. | |||
TMPJ-00938 |
4HPPD Protein, Human, Recombinant (His)
PPD,4HPPD,HPD,4-Hydroxyphenylpyruvate Dioxygenase,H... |
Human | E. coli |
4-Hydroxyphenylpyruvate Dioxygenase (4HPPD) belongs to the 4HPPD family. 4HPPD is a key enzyme in the degradation of tyrosine, which catalyzes the second reaction in the catabolism of tyrosine the conversation of 4-hydroxyphenylpyruvate to homogentisate. 4HPPD exists in homodimer forms, which uses zinc as a cofactor to catalyze the third step in the conversion of L-phenylalanine to fumarate and acetoacetic acid. When the active 4HPPD enzyme concentration is low in the human body, it results in h... | |||
TMPH-02839 |
PLOD2 Protein, Mouse, Recombinant (His & Myc)
Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2,L... |
Mouse | Baculovirus Insect Cells |
Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens. These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links. PLOD2 Protein, Mouse, Recombinant (His & Myc) is expressed in Baculovirus insect cells with C-6xHis-Myc tag. The predicted molecular weight is 85.2 kDa and the accession number is Q9R0B9. | |||
TMPH-02403 |
JBP1 Protein, Leishmania infantum, Recombinant (His & V5)
J-binding protein 1,Thymine dioxygenase JBP1,Thymid... |
Leishmania infantum | E. coli |
JBP1 Protein, Leishmania infantum, Recombinant (His & V5) is expressed in E. coli expression system with N-10xHis-V5 tag. The predicted molecular weight is 53.4 kDa and the accession number is A4HU70. | |||
TMPH-01501 |
HGD Protein, Human, Recombinant (His)
Homogentisicase,Homogentisic acid oxidase,Homogentisate 1,2-... |
Human | E. coli |
HGD Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 54.0 kDa and the accession number is Q93099. | |||
TMPH-00359 |
AlkB Protein, Caulobacter vibrioides, Recombinant (His & Myc)
Alpha-ketoglutarate-dependent dioxygenase AlkB homo... |
Caulobacter vibrioides | E. coli |
AlkB Protein, Caulobacter vibrioides, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 31.2 kDa and the accession number is B8GWW6. | |||
TMPH-02840 |
PLOD2 Protein, Mouse, Recombinant (E. coli, His & Myc)
Lysyl hydroxylase 2,Plod2,Procollagen-lysine,2-oxoglutarate ... |
Mouse | E. coli |
Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens. These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links. | |||
TMPH-01920 |
P4HA3 Protein, Human, Recombinant (His & SUMO)
Prolyl 4-hydroxylase subunit alpha-3,Procollagen-proline,2-o... |
Human | E. coli |
P4HA3 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli. | |||
TMPH-01919 |
P4HA1 Protein, Human, Recombinant (His)
P4HA1,Prolyl 4-hydroxylase subunit alpha-1,Procollagen-proli... |
Human | E. coli |
P4HA1 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPH-01899 |
ALKBH5 Protein, Human, Recombinant (His)
ABH5,Alkylated DNA repair protein alkB homolog 5,RNA demethy... |
Human | E. coli |
ALKBH5 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 48.2 kDa and the accession number is Q6P6C2. | |||
TMPH-00920 |
FTO Protein, Human, Recombinant (His & Myc)
U6 small nuclear RNA (2'-O-methyladenosine-N(6)-)-demethylas... |
Human | E. coli |
FTO Protein, Human, Recombinant (His & Myc) is expressed in E. coli. | |||
TMPY-01736 |
COX-2 Protein, Human, Recombinant (His)
GRIPGHS,PHS-2,hCox-2,COX-2,PGHS-2,prostaglandin-endoperoxide... |
Human | Baculovirus Insect Cells |
PTGS2, also known as COX-2, is s component of Prostaglandin-endoperoxide synthase (PTGS). PTGS, also known as cyclooxygenase, is the key enzyme in prostaglandin biosynthesis, and acts both as a dioxygenase and as a peroxidase. There are two isozymes of PTGS: a constitutive PTGS1 and an inducible PTGS2, which differ in their regulation of expression and tissue distribution. PTGS2 is overexpressed in many cancers. The overexpression of PTGS2 along with increased angiogenesis and GLUT-1 expression ... | |||
TMPH-03606 |
P3H 1 Protein, Streptomyces sp., Recombinant (His & Myc)
Proline 3-hydroxylase type I,L-proline cis-3-hydroxylase 1,P... |
Streptomyces | E. coli |
Dioxygenase that catalyzes the 2-oxoglutarate-dependent selective hydroxylation of free L-proline to cis-3-hydroxy-L-proline (cis-3-Hyp). D-proline, trans-4-hydroxy-L-proline, cis-4-hydroxy-L-proline, cis-4-hydroxy-D-proline, and 3,4-dehydro-DL-proline are not substrates. P3H 1 Protein, Streptomyces sp., Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 44.0 kDa and the accession number is P96010. | |||
TMPY-03658 |
ETHE1 Protein, Human, Recombinant (His)
YF13H12,HSCO,ethylmalonic encephalopathy 1 |
Human | E. coli |
ETHE1, also known as HSCO, is a sulfur dioxygenase that localizes within the mitochondrial matrix. ETHE1 probably plays an important role in metabolic homeostasis in mitochondria. It may also function as a nuclear-cytoplasmic shuttling protein that binds transcription factor RELA/NFKB3 in the nucleus and exports it to the cytoplasm. ETHE1 can suppresses p53-induced apoptosis by preventing nuclear localization of RELA. Mutations in ETHE1 gene result in ethylmalonic encephalopathy. Ethylmalonic en... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T36055 |
Nitisinone-13C6
Nitisinone-13C6 |
||
Nitisinone-13C6is intended for use as an internal standard for the quantification of nitisinone by GC- or LC-MS. Nitisinone is an inhibitor of 4-hydroxyphenylpyruvate dioxygenase (HPPD), which converts 4-hydroxyphenylpyruvate (HPPA) to homogentisate in the tyrosine catabolic pathway.1Nitisinone increases urinary levels of HPPA and 4-hydroxyphenyllactate (HPLA) in rats when administered at a dose of 10 mg/kg. Nitisinone (3 mg/kg) prevents the neonatal lethality of fumarylacetoacetate hydrolase (F... |