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271

抑制剂 & 化合物

6

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T1698	Carvedilol EP IMpurity E Carvedilol USP E,Carvedilol Impurity E,卡维地洛杂质	Others	Others
	Carvedilol EP IMpurity E (Carvedilol USP E) 用作药物中间体。
T1733	Ciprofloxacin EP IMpurity A Q-Acid,Fluoroquinolonic Acid,环丙羧酸,Ciprofloxacin Impurity A	Antibiotic	Microbiology/Virology
	Ciprofloxacin EP IMpurity A (Fluoroquinolonic Acid) 是一种抗生素和抗菌剂。
T8752	BAR 501 impurity	GPCR19	GPCR/G Protein
	BAR 501 impurity 在 BAR501 制剂中发现的一种杂质，可作为 G 蛋白偶联胆汁酸激活受体 (GP-BAR1) 的激动剂。 BAR501 杂质 (10 µM) 在 GP-BAR1 报告基因检测中诱导荧光素酶活性增加 150%。
T31204	Darapladib-impurity	Others	Others
	Darapladib-impurity 是 Darapladib 的杂质。Darapladib 对脂蛋白相关磷脂酶 A2 (Lp-PLA2)有抑制作用。
T11007L	Levofloxacin Hydrochloride Impurity A Levofloxacin Hydrochloride Impurity A(117707-40-1 Free base),左氧氟沙星杂质A(盐酸盐)	Antibacterial	Microbiology/Virology
	Levofloxacin Hydrochloride Impurity A 是一种喹诺酮类药物，具有广谱抗菌作用。
T9042	Teriflunomide impurity 3 4-Amino-N-(4-trifluoromethylphenyl)benzamide	COX	Immunology/Inflammation; Neuroscience
	Teriflunomide impurity 3 (4-Amino-N-(4-trifluoromethylphenyl)benzamide) 是一种选择性COX-1抑制剂，IC50为 30 µM。
T1690	BroMhexine IMpurity B	Others	Others
	BroMhexine IMpurity B 试剂用于制备 Ambroxol 和 Bromhexine (B678600) 代谢物 Ambroxol EP Impurity E。
T0667	Flecainide Impurity D	Others	Others
	Flecainide Impurity D 在工业中用作中间体。
T67853	Rivaroxaban Impurity Rivaroxaban-10	Factor Xa	Metabolism
	Rivaroxaban Impurity (Rivaroxaban-10) 是一种强效凝血因子Xa 抑制剂，IC50=66 nM。
T12962	Sofosbuvir impurity G	HCV Protease	Microbiology/Virology; Proteases/Proteasome
	Sofosbuvir impurity G 是 Sofosbuvir 的非对映异构体，是 Sofosbuvir 的杂质。其中 Sofosbuvir 能够抑制 HCVRNA 的复制，具有抗丙型肝炎病毒作用。
T0550	Domperidone EP Impurity A 5-氯-1,3-二氢-1-(4-哌啶基)-2H-苯并咪唑-2-酮	Others	Others
	Domperidone EP Impurity A 用作医药中间体。
T1357	TriMetazidine EP IMpurity-D	Others	Others
	TriMetazidine EP IMpurity-D 是合成 TriMetazidine 的起始原料，是合成多种化合物的中间体。
T3097	Mycophenolic Acid Impurity 马替麦考酚酸杂质,5,7-dihydroxy-4-methylphthalide	Others	Others
	Mycophenolic Acid Impurity (5,7-dihydroxy-4-methylphthalide) 是一种免疫抑制药物和有效的抗增殖剂，可用于代替旧的抗增殖剂 azathioprine。它通常用作三联疗法的一部分，包括钙调神经磷酸酶抑制剂（ciclosporin 或 tacrolimus）和prednisolone。它还可用于研究选择表达编码 XGPRT（黄嘌呤鸟嘌呤磷酸核糖基转移酶）的大肠杆菌基因的动物细胞。
T4196	Betahistine EP Impurity C NSC19005	Others; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience; Others
	Betahistine EP Impurity C (NSC19005) 是 Betahistine 的杂质。 Betahistine 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂，可用作血管扩张剂，用于类风湿性关节炎的研究。
T9084	Cetirizine Impurity B dihydrochloride De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride,西替利嗪杂质B二盐酸盐,西替利嗪杂质04	Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Cetirizine Impurity B dihydrochloride (De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride) 是 Cetirizine dihydrochloride 的杂质。Cetirizine 是一种抗组胺剂，是口服有活力的、特异性 H1受体拮抗剂。它能够抑制过敏反应期间嗜酸性粒细胞趋化，可以标记抗过敏特性。
T12961	Sofosbuvir impurity F 索非布韦杂质 F,Sofosbuvir 3',5'-Bis-(S)-phosphate	HCV Protease	Microbiology/Virology; Proteases/Proteasome
	Sofosbuvir impurity F (Sofosbuvir 3',5'-Bis-(S)-phosphate) 既是 Sofosbuvir 的非对映异构体，也是 Sofosbuvir 的杂质，Sofosbuvir 是 HCV RNA 复制的抑制剂。
T1689	Enalapril IMpurity B (+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine,依那普利杂质B	Others	Others
	Enalapril IMpurity B ((+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine) 是 Moexipril 中间体，是 Imidapril 的主要代谢物。
T21113	N2-Acetylaciclovir Aciclovir EP Impurity F	Antibacterial	Microbiology/Virology
	N2-Acetylaciclovir (Aciclovir EP Impurity F) 是抗病毒化合物Aciclovir 的衍生物，具有选择性T 细胞免疫毒性。
T32550	Lamivudine impurity A RS Lamivudine impurity A,Lamivudine specified impurity A
	Lamivudine impurity A RS is a bioactive chemical.
T39031	Olmesartan impurity
	Olmesartan impurity, a compound related to Olmesartan, is an angiotensin II receptor (AT1R) antagonist utilized in the study of high blood pressure. Olmesartan (RNH-6270) is the parent compound with similar properties and functions as an AT1R antagonist.
T20997	Amlodipine besilate impurity B Amlodipine EP Impurity B
	Amlodipine besilate impurity B is a biochemical.
T36076	Ciprofibrate impurity A
	Ciprofibrate impurity A is an impurity of Ciprofibrate. Ciprofibrate is a PPARα agonist[1]. [1]. Passilly, P., et al., Phosphorylation of peroxisome proliferator-activated receptor alpha in rat Fao cells and stimulation by ciprofibrate. Biochem Pharmacol, 1999. 58(6): p. 1001-8.
T40537	Ibuprofen Impurity K
	Ibuprofen Impurity K is a compound that serves as an impurity in Ibuprofen. Ibuprofen itself is an anti-inflammatory inhibitor specifically designed to target COX-1 and COX-2. It exhibits inhibitory activity with IC50 values of 13 μM and 370 μM for COX-1 and COX-2, respectively.
T40785	Gefitinib impurity 1
	Gefitinib impurity 1 is a compound derived from Gefitinib, a potent and selective EGFR tyrosine kinase inhibitor (IC 50 = 33 nM). This orally active compound selectively inhibits tumor cell growth stimulated by EGF (IC 50 = 54 nM) and inhibits EGFR autophosphorylation induced by EGF in tumor cells. Additionally, Gefitinib induces autophagy and exhibits antitumor activity.
T1364	7-Aminodeacetoxycephalosporanic acid 7-ADCA,Cephalexin Impurity B,Cefalexine EP IMpurity B,Deacetoxycephalosporanic Acid,头孢氨苄杂质B,7-Aminodesacetoxycephalosporanic acid	Antibiotic	Microbiology/Virology
	7-Aminodeacetoxycephalosporanic acid (Cefalexine EP IMpurity B) 是一种头孢菌素合成中的关键中间体。
T37704	Olanzapine Lactam Impurity
	Olanzapine lactam impurity is a potential impurity found in commercial preparations of olanzapine.1It is a degradation product formed by exposure to thermal or oxidative stress. 1.Baertschi, S.W., Brunner, H., Bunnell, C.A., et al.Isolation, identification, and synthesis of two oxidative degradation products of olanzapine (LY170053) in solid oral formulationsJ. Pharm. Sci.97(2)883-892(2008)
T36945	Cetirizine Impurity C
	Cetirizine Impurity C is an impurity of Cetirizine. Cetirizine is a second-generation antihistamine and the carboxylated metabolite of hydroxyzine. It acts as a specific, orally active, and long-acting antagonist of the histamine H1-receptor[1][2].
T36592	Impurity of Calcipotriol
	Impurity of Calcipotriol 是卡泊三醇的杂质，卡泊三醇是一种合成的 VitD3 类似。
T2692	A40926 Dalbavancin Impurity,达巴霉素杂质	Antibacterial	Microbiology/Virology
	A40926 (Dalbavancin Impurity) 是Dalbavancin 的前体，是一种糖肽抗生素。它抑制革兰氏阳性细菌，对淋病奈瑟氏球菌非常有效。
T37026	Mesalamine impurity P
	Mesalamine impurity P is an impurity of Mesalamine . 5-Aminosalicylic acid (Mesalamine) acts as a specific PPARγ agonist and also inhibits p21-activated kinase 1 (PAK1) and NF-κB[1]. [1]. Kyle Dammann, et al.PAK1 modulates a PPARγ/NF-κB cascade in intestinal inflammation.Biochim Biophys Acta. 2015 Oct;1853(10 Pt A):2349-60.
T37176	Edoxaban impurity 6
	Edoxaban impurity 6 is an impurity of Edoxaban. Edoxaban (DU-176) is a selective, potent and orally active factor Xa (FXa) inhibitor with Kis of 0.561 nM and 2.98 nM for free FXa and prothrombinase, respectively. Edoxaban is an anticoagulant agent and can be used for stroke prevention[1][2]. [1]. Furugohri T, et al. DU-176b, a potent and orally active factor Xa inhibitor: in vitro and in vivo pharmacological profiles. J Thromb Haemost. 2008 Sep;6(9):1542-9.[2]. Mendell J, Lee F, Chen S, The Effe...
T20995	Amlodipine besilate impurity D Amlodipine Related Compound A,Amlodipine impurity A
	Amlodipine besilate impurity D is a biochemical.
T40941	Olmesartan lactone impurity
	Olmesartan lactone impurity is a cyclic ester impurity derived from Olmesartan, which is an angiotensin II receptor (AT1R) antagonist with potential applications in the study of high blood pressure.
T37628	Ibuprofen impurity 1
	Ibuprofen impurity 1 is an Ibuprofen impurity. Ibuprofen is an anti-inflammatory inhibitor targeting COX-1 and COX-2 with IC50s of 13 μM and 370 μM, respectively[1]. [1]. Noreen Y, et al. Development of a radiochemical cyclooxygenase-1 and -2 in vitro assay for identification of natural products as inhibitors of prostaglandin biosynthesis. J Nat Prod. 1998 Jan;61(1):2-7.
T35430	Afatinib impurity 11
	Afatinib impurity 11 is an impurity of Afatinib. Afatinib is an irreversible EGFR family inhibitor with IC50s of 0.5 nM, 0.4 nM, 10 nM and 14 nM for EGFRwt, EGFRL858R, EGFRL858R/T790M and HER2, respectively[1]. [1]. Li D, et al. BIBW2992, an irreversible EGFR/HER2 inhibitor highly effective in preclinical lung cancer models. Oncogene. 2008 Aug 7;27(34):4702-11.
T40752	Ibuprofen Impurity F
	Ibuprofen Impurity F is a known impurity of Ibuprofen, which acts as an anti-inflammatory inhibitor that selectively targets both COX-1 and COX-2 enzymes. It exhibits inhibitory activity with IC50 values of 13 μM and 370 μM for COX-1 and COX-2, respectively.
T35728	Hydrochlorothiazide Impurity C
	Hydrochlorothiazide impurity C is a potential impurity found in commercial hydrochlorothiazide preparations. [1] Hydrochlorothiazide is a thiazide diuretic that inhibits the apical membrane sodium chloride cotransporter in the distal and collecting duct nephron segments.[2][3][4]
T37175	Edoxaban impurity 4
	Edoxaban impurity 4, an impurity of Edoxaban (DU-176), is a selective, potent, and orally active inhibitor of factor Xa (FXa), exhibiting Kis of 0.561 nM for free FXa and 2.98 nM for prothrombinase. As an anticoagulant agent, Edoxaban is utilized for stroke prevention[1][2].
T35876	Chlorthalidone Impurity G
	Chlorthalidone impurity G is a potential impurity found in commercial preparations of chlorthalidone that has moderate antihypertensive effects. Chlorthalidone is a thiazide-like diuretic that inhibits the Na+/Cl- cotransporter in the distal convoluted tubule of the kidney, which prevents reabsorption of sodium and chloride leading to a reduction in plasma volume and cardiac output. It also inhibits carbonic anhydrase (CA), including the isoforms CAVB, VII, IX, XII, and XIII (Kis = 2.8-23 nM) an...
T2025	HDAC-IN-7 HBI-8000,西达本胺杂质,CS055,Chidamide impurity	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC-IN-7 (HBI-8000) 是 Chidamide 的一种杂质。Chidamide 是一种可口服的 HDAC 酶 I 类 HDAC1/2/3 和 IIb 类 HDAC10 抑制剂。
T36006	Olmesartan medoxomil impurity C
	Olmesartan medoxomil impurity C is an Olmesartan medoxomil impurity. Olmesartan medoxomil is a potent and selective angiotensin AT1 receptor inhibitor with IC50 of 66.2 μM. [1]. Senda A, et al. Effects of Angiotensin II Receptor Blockers on Metabolism of Arachidonic Acid via CYP2C8. Biol Pharm Bull. 2015;38(12):1975-9. [2]. Shah S, et al. Simultaneous Quantitative Analysis of Olmesartan Medoxomil and Amlodipine Besylate in Plasma by High-performance Liquid Chromatography Technique. J Young Phar...
T29998	Amlodipine besilate impurity F Amlodipine Dimethyl Ester,Amlodipine USP Related Compound F,Amlodipine EP Impurity F
	Amlodipine besilate impurity F, also known as Amlodipine Dimethyl Ester, is a biochemical.
T10957	Dapagliflozin impurity	Others	Others
	Dapagliflozin impurity is the enantiomer of Dapagliflozin, Dapagliflozin is a sodium glucose transporter 2 inhibitor.
T39885	Captopril EP Impurity E
	Captopril EP Impurity E is an impurity of Captopril. Captopril, also known as SQ-14534, is an orally active angiotensin-converting enzyme (ACE) inhibitor that contains a thiol group. It has antihypertensive properties and competes with ACE with an inhibitor constant (IC 50 ) of 0.025 μM.
T20996	Amlodipine besilate impurity E Amlodipine Diethyl Ester,Amlodipine EP Impurity E,Amlodipine USP Related Compound E
	Amlodipine besilate impurity E is a biochemical.
T0614	4-Amino-5-Chloro-2-Methoxybenzoic Acid 甲氧氯普胺杂质C,Metoclopramide EP Impurity C	Others	Others
	4-Amino-5-Chloro-2-Methoxybenzoic Acid (Metoclopramide EP Impurity C) 是一种Metoclopramide 代谢物。
T11997	MELK-IN-1 Nintedanib Impurity L,MELK inhibitor 17,尼达尼布杂质L	MELK	PI3K/Akt/mTOR signaling
	MELK-IN-1 (MELK inhibitor 17)是一种母体胚胎亮氨酸拉链激酶的有效抑制剂，IC50=3 nM，Ki=0.39 nM。
T38577	Remdesivir O-desphosphate acetonide impurity
	Remdesivir O-desphosphate acetonide impurity is a contaminant found in Remdesivir. Remdesivir (GS-5734) is a nucleoside analogue known for its potent antiviral properties, particularly in inhibiting SARS-CoV-2 (COVID-19) infection in vitro.
T12957	Sofosbuvir impurity B	Others	Others
	Sofosbuvir impurity B is the less active impurity of Sofosbuvir. Sofosbuvir is an active HCV RNA replication inhibitor in the HCV replicon assay, with potent anti-hepatitis C virus (HCV) activity.
T12969	Sofosbuvir impurity N	HCV Protease	Microbiology/Virology; Proteases/Proteasome
	Sofosbuvir impurity N is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.

化合物

Carvedilol EP IMpurity E

Cat.No: T1698

Synonym: Carvedilol USP E,Carvedilol Impurity E,卡维地洛杂质

Target: Others

Ciprofloxacin EP IMpurity A

Cat.No: T1733

Synonym: Q-Acid,Fluoroquinolonic Acid,环丙羧酸,Ciprofloxacin Impurity A

Target: Antibiotic

BAR 501 impurity

Cat.No: T8752

Target: GPCR19

Darapladib-impurity

Cat.No: T31204

Target: Others

Levofloxacin Hydrochloride Impurity A

Cat.No: T11007L

Synonym: Levofloxacin Hydrochloride Impurity A(117707-40-1 Free base),左氧氟沙星杂质A(盐酸盐)

Target: Antibacterial

Teriflunomide impurity 3

Cat.No: T9042

Synonym: 4-Amino-N-(4-trifluoromethylphenyl)benzamide

Target: COX

BroMhexine IMpurity B

Cat.No: T1690

Target: Others

Flecainide Impurity D

Cat.No: T0667

Target: Others

Rivaroxaban Impurity

Cat.No: T67853

Synonym: Rivaroxaban-10

Target: Factor Xa

Sofosbuvir impurity G

Cat.No: T12962

Target: HCV Protease

Domperidone EP Impurity A

Cat.No: T0550

Synonym: 5-氯-1,3-二氢-1-(4-哌啶基)-2H-苯并咪唑-2-酮

Target: Others

TriMetazidine EP IMpurity-D

Cat.No: T1357

Target: Others

Mycophenolic Acid Impurity

Cat.No: T3097

Synonym: 马替麦考酚酸杂质,5,7-dihydroxy-4-methylphthalide

Target: Others

Betahistine EP Impurity C

Cat.No: T4196

Synonym: NSC19005

Target: Others, Histamine Receptor

Cetirizine Impurity B dihydrochloride

Cat.No: T9084

Synonym: De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride,西替利嗪杂质B二盐酸盐,西替利嗪杂质04

Target: Histamine Receptor

Sofosbuvir impurity F

Cat.No: T12961

Synonym: 索非布韦杂质 F,Sofosbuvir 3',5'-Bis-(S)-phosphate

Target: HCV Protease

Enalapril IMpurity B

Cat.No: T1689

Synonym: (+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine,依那普利杂质B

Target: Others

N2-Acetylaciclovir

Cat.No: T21113

Synonym: Aciclovir EP Impurity F

Target: Antibacterial

Lamivudine impurity A RS

Cat.No: T32550

Synonym: Lamivudine impurity A,Lamivudine specified impurity A

Olmesartan impurity

Cat.No: T39031

Amlodipine besilate impurity B

Cat.No: T20997

Synonym: Amlodipine EP Impurity B

Ciprofibrate impurity A

Cat.No: T36076

Ibuprofen Impurity K

Cat.No: T40537

Gefitinib impurity 1

Cat.No: T40785

7-Aminodeacetoxycephalosporanic acid

Cat.No: T1364

Synonym: 7-ADCA,Cephalexin Impurity B,Cefalexine EP IMpurity B,Deacetoxycephalosporanic Acid,头孢氨苄杂质B,7-Aminodesacetoxycephalosporanic acid

Target: Antibiotic

Olanzapine Lactam Impurity

Cat.No: T37704

Cetirizine Impurity C

Cat.No: T36945

Impurity of Calcipotriol

Cat.No: T36592

Cat.No: T2692

Synonym: Dalbavancin Impurity,达巴霉素杂质

Target: Antibacterial

Mesalamine impurity P

Cat.No: T37026

Edoxaban impurity 6

Cat.No: T37176

Amlodipine besilate impurity D

Cat.No: T20995

Synonym: Amlodipine Related Compound A,Amlodipine impurity A

Olmesartan lactone impurity

Cat.No: T40941

Ibuprofen impurity 1

Cat.No: T37628

Afatinib impurity 11

Cat.No: T35430

Ibuprofen Impurity F

Cat.No: T40752

Hydrochlorothiazide Impurity C

Cat.No: T35728

Edoxaban impurity 4

Cat.No: T37175

Chlorthalidone Impurity G

Cat.No: T35876

Cat.No: T2025

Synonym: HBI-8000,西达本胺杂质,CS055,Chidamide impurity

Target: HDAC

Olmesartan medoxomil impurity C

Cat.No: T36006

Amlodipine besilate impurity F

Cat.No: T29998

Synonym: Amlodipine Dimethyl Ester,Amlodipine USP Related Compound F,Amlodipine EP Impurity F

Dapagliflozin impurity

Cat.No: T10957

Target: Others

Captopril EP Impurity E

Cat.No: T39885

Amlodipine besilate impurity E

Cat.No: T20996

Synonym: Amlodipine Diethyl Ester,Amlodipine EP Impurity E,Amlodipine USP Related Compound E

4-Amino-5-Chloro-2-Methoxybenzoic Acid

Cat.No: T0614

Synonym: 甲氧氯普胺杂质C,Metoclopramide EP Impurity C

Target: Others

Cat.No: T11997

Synonym: Nintedanib Impurity L,MELK inhibitor 17,尼达尼布杂质L

Target: MELK

Remdesivir O-desphosphate acetonide impurity

Cat.No: T38577

Sofosbuvir impurity B

Cat.No: T12957

Target: Others

Sofosbuvir impurity N

Cat.No: T12969

Target: HCV Protease

Cat. No.	Product Name	Target	Signaling Pathways
TN5757	p-Hydroxybenzaldehyde glucoside 4-formylphenyl b-d-glucopyranoside,Gastrodin Impurity
	p-Hydroxybenzaldehyde glucoside (4-formylphenyl b-d-glucopyranoside) 是抑制天麻素衍生物，具有镇痛活性，可以用于研究神经源性疼痛。
TN7045	N-phenethylbenzamide N-(2-Phenylethyl)benzamide,Solina New Impurity 21,N-苯乙基-苯甲酰胺,4-(DICHLOROMETHYL)PYRIDINE HCL	Others	Others
	N-phenethylbenzamide (Solina New Impurity 21) 是一种天然产物。
TN7036	N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamide (9Z,12Z,15Z)-N-[(3-Methoxyphenyl)methyl]-9,12,15-octadecatrienamide,间-甲氧基苄基-亚麻酰胺,Macamide Impurity 14	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamide (Macamide Impurity 14) 是一种从玛卡中分离得到的玛卡酰胺。它能够激活典型的Wnt/β‐catenin 信号通路，诱导间充质干细胞成骨分化和随后的骨形成，可用于研究骨质疏松症。
TN7064	Candicine 4-Hydroxy-N-Benzeneethanaminium,N, N, N-trimethyltyramine chloride,Candicin,N-Methylhordenine,Tyramine Impurity 1,4-羟基-N,N,N-三甲基-苯乙铵,2-(4-hydroxyphenyl)ethyl-trimethylazanium	Others	Others
	Candicine (N, N, N-trimethyltyramine chloride) 是来自 Stapelia gigantea 的天然产品。
TN6498	Stevia impurity (13-[(2-O-6-deoxy-Î²-D-glucopyranosyl-3-O-Î²-D-glucopyranosyl-Î²-D-glucopyranosyl)oxy]ent-kaur-16-en-19-oic acid Î²-D-glucopyranosyl ester)
	Stevia impurity (13-[(2-O-6-deoxy-Î²-D-glucopyranosyl-3-O-Î²-D-glucopyranosyl-Î²-D-glucopyranosyl)oxy]ent-kaur-16-en-19-oic acid Î²-D-glucopyranosyl ester) 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN6498，CAS号为 1309929-72-3。
TN1352	N-(3-Methoxybenzyl-(9z,12z)-octadecadienamide 12顺-亚油酸酰胺,(9Z,12Z)-N-(3-Methoxybenzyl)octadeca-9,12-dienamide,n-3-methoxybenzyl-9z-12z-octadecadienamide,玛卡酰胺杂质10	Drug Metabolite	Metabolism
	N-(3-Methoxybenzyl-(9z,12z)-octadecadienamide ((9Z,12Z)-N-(3-Methoxybenzyl)octadeca-9,12-dienamide) 是一种 Macamide 杂质，可能用于代谢疾病的研究。

天然产物

p-Hydroxybenzaldehyde glucoside

Cat.No: TN5757

Synonym: 4-formylphenyl b-d-glucopyranoside,Gastrodin Impurity

N-phenethylbenzamide

Cat.No: TN7045

Synonym: N-(2-Phenylethyl)benzamide,Solina New Impurity 21,N-苯乙基-苯甲酰胺,4-(DICHLOROMETHYL)PYRIDINE HCL

Target: Others

N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamide

Cat.No: TN7036

Synonym: (9Z,12Z,15Z)-N-[(3-Methoxyphenyl)methyl]-9,12,15-octadecatrienamide,间-甲氧基苄基-亚麻酰胺,Macamide Impurity 14

Target: Wnt/beta-catenin

Cat.No: TN7064

Synonym: 4-Hydroxy-N-Benzeneethanaminium,N, N, N-trimethyltyramine chloride,Candicin,N-Methylhordenine,Tyramine Impurity 1,4-羟基-N,N,N-三甲基-苯乙铵,2-(4-hydroxyphenyl)ethyl-trimethylazanium

Target: Others

Stevia impurity (13-[(2-O-6-deoxy-Î²-D-glucopyranosyl-3-O-Î²-D-glucopyranosyl-Î²-D-glucopyranosyl)oxy]ent-kaur-16-en-19-oic acid Î²-D-glucopyranosyl ester)

Cat.No: TN6498

N-(3-Methoxybenzyl-(9z,12z)-octadecadienamide

Cat.No: TN1352

Synonym: 12顺-亚油酸酰胺,(9Z,12Z)-N-(3-Methoxybenzyl)octadeca-9,12-dienamide,n-3-methoxybenzyl-9z-12z-octadecadienamide,玛卡酰胺杂质10

Target: Drug Metabolite

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