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61

抑制剂 & 化合物

6

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Cat. No. Product Name Target Signaling Pathways
T10917 LTB4-IN-1

Anti-inflammatory agent 2

LTR Immunology/Inflammation
LTB4-IN-1 (Anti-inflammatory agent 2) 是白三烯 (LTB4) 合成抑制剂,IC50 为 70 nM。
T78678 LTB4 antagonist 3

Leukotriene Receptor GPCR/G Protein
LTB4 antagonist 3 (compound 24e)为一种具有抗炎活性的LTB4拮抗剂,其IC50为477 nM。
T78677 LTB4 antagonist 2

Leukotriene Receptor GPCR/G Protein
LTB4 antagonist 2为甲酰胺化合物,白三烯B4 (LTB4) 拮抗剂,显示抗炎潜能。该化合物对LTB4受体亲和力高,IC50值为439 nM。
T72625 LTB4 antagonist 1

Leukotriene Receptor GPCR/G Protein
LTB4 antagonist 1为甲酰胺化合物,高效拮抗白三烯B4 (LTB4),IC50值为288 nM,呈现出明显的抗炎活性。
T79389 LTB4-IN-2

FLAP Immunology/Inflammation
LTB4-IN-2(Compound 6x)是一种选择性的5-脂氧合酶激活蛋白(FLAP)抑制剂,旨在抑制白三烯B4LTB4)的形成(IC50:1.15 μM),适用于抗炎研究。
T22946 LY255283

LY 255283

Leukotriene Receptor GPCR/G Protein
LY255283 是白三烯 B4 (LTB4) 受体的特异性拮抗剂,抑制人外周血多形核白细胞和由钙离子载体 A23187 激活的单核细胞中 LTB(4) 的产生。
T14045 Leukotriene B4

LTB4,5(S),12(R)-DiHETE

Others Others
Leukotriene B4 is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].
T17191 Bunaprolast

U66858

Lipoxygenase; LTR Immunology/Inflammation; Metabolism
Bunaprolast (U66858) 是一种新型有效的白三烯 B4 (LTB4) 抑制剂。Bunaprolast 具有氧化降解活性,对脂氧合酶 (lipoxygenase)和 TXB2 释放具有抑制作用。
T15002 CP-105696

Pfizer 105696

LTR Immunology/Inflammation
CP-105696 是一种具有强效性和选择性白三烯 B4 (LTB4) 受体拮抗剂,可用于研究异体移植物排斥反应。
T11487 Fiboflapon

GSK2190915,AM-803

FLAP Immunology/Inflammation
Fiboflapon (GSK2190915) 是一种可口服且具有有效性 5-脂氧合酶激活蛋白 (FLAP) 抑制剂,结合 FLAP 的效价为 2.9 nM,对人血中 LTB4 有抑制作用, IC50 值为 76 nM。
T28974 Ticolubant

Calcium Channel; LTR Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
Ticolubant 是一种具有口服活性的白三烯 B4 拮抗剂,对人类中性粒细胞 LTB4 受体具有很高的亲和力(Ki = 0.78 nM),能阻断 LTB4 诱导的 Ca2+ 迁移,IC50 为 6.6±1.5 nM,并在小鼠皮肤炎症模型中显示出局部抗炎活性。
T22358 Etalocib

LY293111,VML295

Apoptosis; Leukotriene Receptor; LTR Apoptosis; GPCR/G Protein; Immunology/Inflammation
Etalocib (LY293111) 是一种具有口服活性的白三烯(LTB4)受体的拮抗剂,抑制 [3H]LTB4结合的 Ki 值为 25 nM。它还可诱导凋亡。它抑制 LTB4诱导的钙动员,lC50值为 20 nM。
T10960L Darbufelone mesylate

CI-1004 mesylate

Prostaglandin Receptor; LTR GPCR/G Protein; Immunology/Inflammation
Darbufelone mesylate (CI-1004 mesylate) 对细胞中 PGF2α 和 LTB4 产生有抑制作用。Darbufelone mesylate 对 PGHS-2 有抑制作用,IC50 值为 0.19 μM,对 PGHS-1 的IC50 值为 20 μM。
T9878 Croconazole

Lipoxygenase; LTR Immunology/Inflammation; Metabolism
Croconazole 对中性粒细胞的 5-脂氧合酶 (5-LOX) 表现出剂量依赖性抑制活性。Croconazole 是一种抗真菌剂。Croconazole 对合成白三烯 B4 (LTB4) 和 5-羟基二十碳四烯酸 (5-HETE) 的 IC50 分别为 7.8 ± 1.7 和 7.6 ± 0.3 μM。
T68155 Tebufelone

Prostaglandin Receptor; LTR GPCR/G Protein; Immunology/Inflammation
Tebufelone 是一种体外高效的CO 抑制剂 ,是一种新型的非甾体抗炎药(NSAID),属于二叔丁基苯酚(DTBP)类,在各种动物模型中显示出强大的抗炎、镇痛和抗网膜炎特性。Tebufelone 能有效地抑制前列腺素(PGE2)的形成,阻止大鼠巨噬细胞(IC50 = 20 microM)和人类全血(IC50 = 22 microM)中脂氧酶途径的产物[白三烯(LTB4)]的体外形成。
T10960 Darbufelone

达布非酮,CI-1004

Prostaglandin Receptor; LTR GPCR/G Protein; Immunology/Inflammation
Darbufelone (CI-1004) 是 PGF2α 和 LTB4 的非竞争性双重抑制剂。 Dabfilon 有效抑制 PGHS-2,对 PGHS-2 和 PGHS-1 的 Ki 为 10 μM,IC50 为 0.19 μM 和 20 μM。
T11699 J-113863

CCR Immunology/Inflammation; Microbiology/Virology
J-113863 是选择性的 CCR1 (CD18)拮抗剂,有抗炎作用,对人和小鼠 CCR1受体的 IC50值分别为 0.9 和 5.8 nM。它是人 CCR3的强效拮抗剂,还是小鼠 CCR3的弱效拮抗剂,IC50分别为 0.58 和 460 nM。
T16395 ONO4057

ONO-LB457

Leukotriene Receptor GPCR/G Protein
ONO4057 是一种具有有效性和口服活性的 Leukotriene B4 受体拮抗剂,其 IC50 值为 0.7±0.3 μM。 ONO4057 对大鼠同种异体移植的免疫抑制作用。
T15801 LY210073

Others Others
LY210073 is an antagonist of the Leukotriene B4 (LTB4) receptor (IC50: 6.2 nM).
T10208 A-69412

N-1-(Fur-3-ylethyl)-N-hydroxyurea

Lipoxygenase Metabolism
A-69412 (N-1-(Fur-3-ylethyl)-N-hydroxyurea) 是一种特异性的 5-脂氧合酶 (5-LO) 的可逆抑制剂。 A-69412 能用于哮喘和溃疡性结肠炎,以及其他炎症和过敏症状的研究。
T15803 LY223982

SKF107324,CGS23131

Others Others
LY223982 is an effective and specific inhibitor of the leukotriene B4 receptor (IC50: 13.2 nM). It also can against [3H]LTB4 binding to LTB4 receptor.
T38087 20-hydroxy Leukotriene B4

20-hydroxy Leukotriene B4

20-hydroxy LTB4 is a metabolite of LTB4 in human neutrophils. In human leukocytes, LTB4 is inactivated by the enzyme LTB4 20-hydroxylase. 20-hydroxy LTB4 is not only much less active (~5%) compared to LTB4 in causing degranulation of PMNL, but actually inhibits LTB4-induced degranulation of human neutrophils (Ki = 13.3 nM). However, 20-hydroxy LTB4 is as active as LTB4 in contracting parenchymal strips from guinea pig lung. 20-hydroxy LTB4 retains considerable ligand binding affinity at the BLT2...
T11487L Fiboflapon sodium

GSK2190915 sodium salt,AM-803 sodium

LTR Immunology/Inflammation
Fiboflapon sodium (GSK2190915) is an orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.
T1544 Olsalazine disodium

Dipentum,奥沙拉秦钠,Olsalazine Sodium

Others; COX; Antibacterial; Antibiotic Immunology/Inflammation; Microbiology/Virology; Neuroscience; Others
Olsalazine disodium (Dipentum) 是抗炎化合物,可作用于溃疡性结肠炎和炎症性肠病。
T10543 BIIL-260 hydrochloride

Others Others
BIIL-260 hydrochloride is a potent and long-acting orally active antagonist of leukotriene B4 (LTB4) receptor with anti-inflammatory activity. It has a high affinity to the LTB4 receptor on isolated human neutrophil cell membranes (Ki: 1.7 nM).
T14210 Amelubant

BIIL 284

LTR Immunology/Inflammation
Amelubant (BIIL 284) is a prodrug of active metabolites BIIL 260 and BIIL 315. Anti-inflammatory activity[1]. Amelubant (BIIL 284) is a potent, oral and long acting LTB4 receptor antagonist, negligibly binds to LTB4 receptor, with Kis of 221 nM and 230 nM
T34555 SC 45694

SC45694,SC-45694

SC 45694 is a leukotriene B4 (LTB4) analog.
T37619 Leukotriene B4 Ethanolamide

The effects of Leukotriene B4 (LTB4) are mediated by two known receptors, BLT1 and BLT2. LTB4 is a high affinity ligand for BLT1, and many of its pro-inflammatory effects are believed to be transduced through this receptor. The BLT2 is more enigmatic, in that LTB4 is not a high-affinity ligand, nor is it clear that BLT2 activation promotes inflammation. LTB4 ethanolamide (LTB4-EA) is a theoretical 5-LO metabolite of arachidonoyl ethanolamide (AEA). In CHO cells transfected with human BLTR1, LTB4...
T37260 14,15-dehydro Leukotriene B4

14,15-dehydro Leukotriene B4

Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from arachidonic acid through the 5-lipoxygenase pathway. It promotes a number of leukocyte functions including aggregation, stimulation of ion fluxes, enhancement of lysosomal enzyme release, superoxide anion production, chemotaxis, and chemokinesis. At least two LTB4 receptors, termed BLT1 and BLT2, have been identified. 14,15-dehydro LTB4 is a LTB4 receptor antagonist that has a higher binding affinity for BLT1, demonstrating a Ki value ...
T22526 BML-111

5(S),6(R)-7-trihydroxymethyl Heptanoate

Others Others
inhibits leukotriene B4 (LTB4)-induced polymorphonuclear neutrophils (PMN) chemotaxis
T73793 20-Carboxy-Leukotriene B4

20-Carboxy-Leukotriene B4 (20-COOH LTB4) 是 Leukotriene B4 (LTB4) 的代谢物。20-Carboxy-Leukotriene B4 以高亲和力与 BLT1 受体结合。20-Carboxy-Leukotriene B4 抑制 LTB4 介导的中性粒细胞反应,迁移、脱粒、白三烯生物合成。
T37256 12-oxo Leukotriene B4

12-oxo Leukotriene B4

Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from arachidonic acid through the 5-LO pathway. It promotes a number of leukocyte functions including aggregation, stimulation of ion fluxes, enhancement of lysosomal enzyme release, superoxide anion production, chemotaxis, and chemokinesis. 12-oxo LTB4 is an initial metabolite of LTB4 formed via the LTB4 12-hydroxydehydrogenase pathway. It is rapidly converted to 10,11-dihydro-12-oxo-LTB4, followed by reduction of the 12-oxo group to give ...
T37970 12-epi Leukotriene B4

12-epi Leukotriene B4

Leukotriene B4 (LTB4) compounds are produced by both enzymatic and non-enzymatic processes. The products of enzymatic origin, via Leukotriene A4 (LTA4) hydrolase, are stereospecifically 12(R). Non-enzymatic hydrolysis products are 50:50 mixtures at C-12, but are almost exclusively trans at C-6. Thus, the non-enzymatic hydrolysis product of LTA4 is 6-trans-12-epi LTB4. 12-epi LTB4 is an isomer which would not be expected to occur in either non-enzymatic hydrolysis products, or in the enzymatic pr...
T38157 Ricinelaidic Acid

Ricinelaidic acid is a 12-hydroxy fatty acid and an antagonist of leukotriene B4 (LTB4) receptors (Ki = 2 μM in porcine neutrophil membranes). It inhibits chemotaxis and calcium flux induced by LTB4 in isolated human neutrophils (IC50s = 10 and 7 μM, respectively). Ricinelaidic acid (1 mg/kg, i.v.) inhibits bronchoconstriction induced by LTB4 in rats by 46%.
T15182 DW-1350

LTR Immunology/Inflammation
DW-1350 is an antagonist of LTB4 receptor.
T37618 Leukotriene B4 dimethyl amide

Leukotriene B4 dimethyl amide

LTB4 dimethyl amide is a moderate inhibitor of LTB4-induced degranulation of human neutrophils (Ki = 130 nM) and lysozyme release from rat PMNL. LTB4 dimethyl amide appears to be an antagonist of the LTB4 receptor on guinea pig lung membranes.
T70799 SC-50605

SC-50605 is a second-generation LTB4 receptor antagonist.
T71499 NZ-107

NZ-107 is an LTB4, LTC4 and LTD4 antagonist.
T28602 RO5101576

RO-5101576,RO 5101576

RO5101576 is a potent antagonist of LTB4 receptor.
T37617 Leukotriene B3

LTB3 is the LTA hydrolase metabolite of LTA3 in the leukotriene biosynthetic pathway. LTB3 and LTB4 are equipotent in their pro-inflammatory effects. However, LTB3 is five times less potent than LTB4 in eliciting chemotaxis of human neutrophils.
T71283 JNJ-40929837

JNJ-40929837 is an oral inhibitor of LTA4 hydrolase, which catalyzes LTB4 production.
T70563 KC-11404

KC-11404 is an LTB4 inhibitor for the treatment of b-cell leukemias and lymphomas, potently inhibiting histamine, platelet activating factor and 5-lipoxygenase.
T23895 WF 11605

WF11605,WF-11605

WF 11605 is an antagonist of leukotriene B4 produced by a fungus and is a specific antagonist of LTB4.
T15825 LY 178002

Retinoid Receptor Metabolism
LY 178002 is an effective inhibitor of 5-lipoxygenase (5-LPO), phospholipase A2 (IC50: 0.6 μM for 5-lipoxygenase). LY 178002 also inhibits cellular production of LTB4 by human polymorphonuclear leukocytes and displays relatively weak inhibition on cycloox
T37460 Lipoxin B4

Lipoxin B4

Lipoxin B4 (LXB4) is a positional isomer of LXA4 produced by the metabolism of 15-HETE or 15(S)-HpETE by human leukocytes. At a concentration of 100 nM, LXB4 inhibits polymorphonuclear leukocyte (PMN) migration stimulated by leukotriene B4 and inhibits LTB4-induced adhesion of PMNs with an IC50 value of 0.3 nM.
T37156 8(S),15(S)-DiHETE

8(S),15(S)-DiHETE is formed when 15(S)-HETE is subjected to further oxidation by 15-LO. It causes eosinophil chemotaxis with an ED50 value of 1.5 μM but is not chemotactic for neutrophils. 8(S),15(S)-DiHETE antagonizes the hyperalgesic activity of 8(R),15(S)-DiHETE and LTB4 in the rat hind paw pain model.
T24970 1'-Ethylascorbigen

1'-Ethylascorbigen releases ascorbic acid in acidic solution results in an increase in the cells' ability to produce PGE2 & LTB4. It has been shown to inhibit the growth of experimental murine tumors.
T71053 AHR-5333 mandelate

AHR-5333 mandelate is an anti-allergy compound which has been shown to protect against antigen-induced anaphylactic collapse and ascaris antigen-induced skin hypersensitivity. AHR-5333 mandelate has also been shown to inhibit 5-HETE, LTB4 and LTC4 synthesis.
T38308 Lipoxin B4 methyl ester

Lipoxin B4 (LXB4) methyl ester is a lipid soluble prodrug form of the transcellular metabolite LXB4 . LXB4 is a positional isomer of LXA4 produced by the metabolism of 15-HETE or 15-HpETE by human leukocytes. At a concentration of 100 nM, LXB4 inhibits polymorphonuclear leukocyte (PMN) migration stimulated by leukotriene B4 and inhibits LTB4-induced adhesion of PMNs with an IC50 value of 0.3 nM.
T37650 5(S),15(S)-DiHETE

5(S),15(S)-DiHETE is synthesized by 15-LO from 5(S)-HETE. It potentiates the degranulation of human PMNL in response to PAF, but not fMLP, calcium ionophore A23187, or LTB4. 5(S),15(S)-DiHETE is chemotactic for eosinophils with an ED50 value of 0.3 μM.

化合物

LTB4-IN-1
Cat.No: T10917
Synonym: Anti-inflammatory agent 2
Target: LTR
LTB4 antagonist 3
Cat.No: T78678
Synonym:
Target: Leukotriene Receptor
LTB4 antagonist 2
Cat.No: T78677
Synonym:
Target: Leukotriene Receptor
LTB4 antagonist 1
Cat.No: T72625
Synonym:
Target: Leukotriene Receptor
LTB4-IN-2
Cat.No: T79389
Synonym:
Target: FLAP
LY255283
Cat.No: T22946
Synonym: LY 255283
Target: Leukotriene Receptor
Leukotriene B4
Cat.No: T14045
Synonym: LTB4,5(S),12(R)-DiHETE
Target: Others
Bunaprolast
Cat.No: T17191
Synonym: U66858
Target: Lipoxygenase, LTR
CP-105696
Cat.No: T15002
Synonym: Pfizer 105696
Target: LTR
Fiboflapon
Cat.No: T11487
Synonym: GSK2190915,AM-803
Target: FLAP
Ticolubant
Cat.No: T28974
Synonym:
Target: Calcium Channel, LTR
Etalocib
Cat.No: T22358
Synonym: LY293111,VML295
Target: Apoptosis, Leukotriene Receptor, LTR
Darbufelone mesylate
Cat.No: T10960L
Synonym: CI-1004 mesylate
Target: Prostaglandin Receptor, LTR
Croconazole
Cat.No: T9878
Synonym:
Target: Lipoxygenase, LTR
Tebufelone
Cat.No: T68155
Synonym:
Target: Prostaglandin Receptor, LTR
Darbufelone
Cat.No: T10960
Synonym: 达布非酮,CI-1004
Target: Prostaglandin Receptor, LTR
J-113863
Cat.No: T11699
Synonym:
Target: CCR
ONO4057
Cat.No: T16395
Synonym: ONO-LB457
Target: Leukotriene Receptor
LY210073
Cat.No: T15801
Synonym:
Target: Others
A-69412
Cat.No: T10208
Synonym: N-1-(Fur-3-ylethyl)-N-hydroxyurea
Target: Lipoxygenase
LY223982
Cat.No: T15803
Synonym: SKF107324,CGS23131
Target: Others
20-hydroxy Leukotriene B4
Cat.No: T38087
Synonym: 20-hydroxy Leukotriene B4
Target:
Fiboflapon sodium
Cat.No: T11487L
Synonym: GSK2190915 sodium salt,AM-803 sodium
Target: LTR
Olsalazine disodium
Cat.No: T1544
Synonym: Dipentum,奥沙拉秦钠,Olsalazine Sodium
Target: Others, COX, Antibacterial, Antibiotic
BIIL-260 hydrochloride
Cat.No: T10543
Synonym:
Target: Others
Amelubant
Cat.No: T14210
Synonym: BIIL 284
Target: LTR
SC 45694
Cat.No: T34555
Synonym: SC45694,SC-45694
Target:
Leukotriene B4 Ethanolamide
Cat.No: T37619
Synonym:
Target:
14,15-dehydro Leukotriene B4
Cat.No: T37260
Synonym: 14,15-dehydro Leukotriene B4
Target:
BML-111
Cat.No: T22526
Synonym: 5(S),6(R)-7-trihydroxymethyl Heptanoate
Target: Others
20-Carboxy-Leukotriene B4
Cat.No: T73793
Synonym:
Target:
12-oxo Leukotriene B4
Cat.No: T37256
Synonym: 12-oxo Leukotriene B4
Target:
12-epi Leukotriene B4
Cat.No: T37970
Synonym: 12-epi Leukotriene B4
Target:
Ricinelaidic Acid
Cat.No: T38157
Synonym:
Target:
DW-1350
Cat.No: T15182
Synonym:
Target: LTR
Leukotriene B4 dimethyl amide
Cat.No: T37618
Synonym: Leukotriene B4 dimethyl amide
Target:
SC-50605
Cat.No: T70799
Synonym:
Target:
NZ-107
Cat.No: T71499
Synonym:
Target:
RO5101576
Cat.No: T28602
Synonym: RO-5101576,RO 5101576
Target:
Leukotriene B3
Cat.No: T37617
Synonym:
Target:
JNJ-40929837
Cat.No: T71283
Synonym:
Target:
KC-11404
Cat.No: T70563
Synonym:
Target:
WF 11605
Cat.No: T23895
Synonym: WF11605,WF-11605
Target:
LY 178002
Cat.No: T15825
Synonym:
Target: Retinoid Receptor
Lipoxin B4
Cat.No: T37460
Synonym: Lipoxin B4
Target:
8(S),15(S)-DiHETE
Cat.No: T37156
Synonym:
Target:
1'-Ethylascorbigen
Cat.No: T24970
Synonym:
Target:
AHR-5333 mandelate
Cat.No: T71053
Synonym:
Target:
Lipoxin B4 methyl ester
Cat.No: T38308
Synonym:
Target:
5(S),15(S)-DiHETE
Cat.No: T37650
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T21504 γ-Linolenic Acid methyl ester

Methyl gamma-linolenate,γ-亚麻酸甲酯

LTR Immunology/Inflammation
γ-Linolenic Acid methyl ester (Methyl gamma-linolenate) 是一种弱白三烯 B4 (LTB4) 受体拮抗剂。
T7786 Tryptanthrin

DNA gyrase DNA Damage/DNA Repair
Tryptanthrin 是一种口服具有活性的细胞内Leukotriene (LT) biosynthesis 抑制剂。 它能够降低大鼠胸膜炎模型中的 LTB4 水平,并抑制人全血中Leukotriene 的形成 (IC50= 10 µM)。
T3868 Agnuside

牡荆油,穗花牡荆苷,chasteberry oil

COX; Prostaglandin Receptor; P-gp GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience
Agnuside (chasteberry oil) 是从黄荆中分离得到的一种天然产物,可下调炎性介质PGE2和LTB4,减少细胞因子的表达,具有抗关节炎活性。
T13661 Docosatrienoic Acid

cis-13,16,19-docosatrienoic acid,(13Z,16Z,19Z)-13,16,19-Docosatrienoic acid

Others Others
Docosatrienoic acid is a rare omega-3 fatty acid; Ki value is 5×M, which inhibits the binding of LTB4 to porcine neutrophil membrane.
T4114 Diffractaic Acid

NSC 5901,地弗地衣酸,NSC 685595

Apoptosis; LTR Apoptosis; Immunology/Inflammation
Diffractaic Acid (NSC 685595) 是松萝的主要成分,具有止痛和解热效果,在各种疾病研究中可作为有效的促凋亡剂。
TN5164 trans-Hinokiresinol

IL Receptor; TNF; NOS; LTR Apoptosis; Immunology/Inflammation
Hinokiresinol is a novel inhibitor of LTB4 binding to the human neutrophils, it has antiallergic effect, it inhibits IgE-induced mouse passive cutaneous anaphylaxis reaction. Hinokiresinol (trans-hinokiresinol) and nyasol (cis-hinokiresinol) are estrogen

天然产物

γ-Linolenic Acid methyl ester
Cat.No: T21504
Synonym: Methyl gamma-linolenate,γ-亚麻酸甲酯
Target: LTR
Tryptanthrin
Cat.No: T7786
Synonym:
Target: DNA gyrase
Agnuside
Cat.No: T3868
Synonym: 牡荆油,穗花牡荆苷,chasteberry oil
Target: COX, Prostaglandin Receptor, P-gp
Docosatrienoic Acid
Cat.No: T13661
Synonym: cis-13,16,19-docosatrienoic acid,(13Z,16Z,19Z)-13,16,19-Docosatrienoic acid
Target: Others
Diffractaic Acid
Cat.No: T4114
Synonym: NSC 5901,地弗地衣酸,NSC 685595
Target: Apoptosis, LTR
trans-Hinokiresinol
Cat.No: TN5164
Synonym:
Target: IL Receptor, TNF, NOS, LTR
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