96
25
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23965 |
DAT 582
DAT582,DAT-582 |
||
DAT 582 is a novel serotonin3 receptor antagonist. It is also an effective and long-lasting antiemetic agent | |||
T70527 |
DAT-230
|
||
DAT-230 is a promising microtubule inhibitor that has great potential for the treatment of fibrosarcoma in vitro and in vivo. DAT-230 exhibited potent anti-proliferative activity against various cancer cells. DAT-230 -treatment in HT-1080 cells resulted in microtubule de-polymerization and G2/M phase arrest preceding apoptosis. Phosphor-cdc2 (thr14/tyr15) reduction, cyclin B1 accumulation and aberrant spindles denoted the cyclin B1-cdc2 complex active and M phase arrest in HT-1080 cells treated ... | |||
T25290 |
DAT1
DAT-1,DAT 1 |
||
DAT1 is an antimitotic and antiangiogenic that acts by binding to the colchicine binding site of tubulin. | |||
T0322 |
Fipexide
|
Dopamine Receptor; AChR | GPCR/G Protein; Neuroscience |
Fipexide 是对氯苯乙酸衍生物,是哌嗪化学类的精神活性药物,作为促智药物,有用于老年痴呆的研究潜力。它可降低了纹状体腺苷酸环化酶的活性,通过多巴胺能神经传递对认知表现出积极的作用。 | |||
T6414 |
Bisacodyl
比沙可啶,Fenilaxan,Dulcolax,Brocalax |
Others | Others |
Bisacodyl (Fenilaxan) 是刺激性缓泻剂,可直接作用于结肠以产生排便。它能够直接激活结肠巨噬细胞来增加 PGE2的分泌。PGE2充当旁分泌因子并减少结肠中 AQP3 的表达,抑制水从腔向血管一侧的转移,进而产生通便作用。 | |||
T22714 |
Decynium 22
|
Others | Others |
Decynium 22 是有机阳离子转运蛋白和单胺转运蛋白的抑制剂,具有抗抑郁作用。 | |||
T70525 | ARC39 | ||
ARC39 is acid sphingomyelinase inhibitor (IC50 =20 nM). | |||
T1871 |
GBR 12935 dihydrochloride
GBR12935,GBR-12935,GBR 12935 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
GBR 12935 dihydrochloride (GBR 12935) 是一种多巴胺再吸收抑制剂。 | |||
T1993 |
J-147
J147 |
Epigenetic Reader Domain; Dopamine Receptor; Monoamine Oxidase | Chromatin/Epigenetic; GPCR/G Protein; Neuroscience |
J-147 是一种高效的、具有口服活性的、可透过血脑屏障神经保护剂,可增强认知能力。它抑制单胺氧化酶 B 和多巴胺转运体,EC50分别为 1.88 μM 和 0.649 μM。它有研究阿尔茨海默氏症的潜力。 | |||
T11087 |
DOV-216,303 Free Base
DOV-216303 |
Dopamine Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
DOV-216,303 Free Base (DOV-216303) 是血清素、去甲肾上腺素和多巴胺再摄取的抑制剂,IC50 为 14、20 和 78 nM。 DOV-216,303 Free Base 具有抗抑郁作用。 | |||
T39429 |
AHN 1-055 hydrochloride
3α-Bis-(4-fluorophenyl) Methoxytropane hydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
AHN 1-055 hydrochloride (3α-Bis-(4-fluorophenyl) Methoxytropane hydrochloride) 与多巴胺转运蛋白具有高亲和力,是多巴胺摄取抑制剂,IC50为 71 nM。 | |||
T10758L |
Centanafadine hydrochloride
EB-1020 hydrochloride |
Dopamine Receptor; Serotonin Transporter; Adrenergic Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Centanafadine hydrochloride (EB-1020 hydrochloride) 是一种去甲肾上腺素(NE)/多巴胺(DA)转运的双抑制剂,还能抑制5-羟色胺(serotonin)转运体。它对人 NE,DA 和5-羟色胺转运体的 IC50值分别为6 nM,38 nM 和 83 nM。 | |||
T3526 |
Dasotraline hydrochloride
SEP-225289 hydrochloride,达索曲林盐酸盐 |
Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
Dasotraline hydrochloride (SEP-225289 hydrochloride) 是具有阻断多巴胺 (IC50=4 nM),去甲肾上腺素 (IC50=6 nM) 和三羟色胺转运蛋白 (IC50=11 nM)的三重再摄取抑制剂。 | |||
T7745 |
Diclofensine hydrochloride
4-(3,4-二氯苯)-7-甲氧基-2-甲基-1,2,3,4-四氢异喹啉盐酸盐,Ro 8-4650 hydrochloride |
Others; Dopamine Receptor | GPCR/G Protein; Neuroscience; Others |
Diclofensine hydrochloride (Ro 8-4650 hydrochloride) 是一种高效单胺再摄取抑制剂,在大鼠脑突触体中能够阻断多巴胺 (IC50=0.74 nM)、去甲肾上腺素 (IC50=2.3 nM) 和 5-羟色胺 (IC50=3.7 nM)。 | |||
T2092 |
Amitifadine hydrochloride
DOV-21947 hydrochloride,EB-1010 hydrochloride |
Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
Amitifadine hydrochloride (EB-1010 hydrochloride) 是一种 5-羟色胺-去甲肾上腺素-多巴胺的再摄取抑制剂(SNDRI),其在 HEK 293 细胞中测得的 IC50值分别为 12, 23, 96 nM。 | |||
T69807 |
EGFR-IN-451
|
||
EGFR-IN-451 is an EGFR inhibitor, attenuating Ang II-induced Kidney Fibrosis. | |||
T7153 |
Vanoxerine dihydrochloride
GBR-12909 dihydrochloride,伐诺司林二盐酸盐,I893 dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) 是一种竞争性的、有效的、选择性的多巴胺再摄取抑制剂,能够与多巴胺转运体 (DAT) 上的靶点结合。 | |||
T0991 |
Desipramine hydrochloride
NSC-114901,Desmethylimipramine,盐酸去甲咪嗪,JB-8181,EX-4355,Norimipramine,G-35020 |
Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Desipramine hydrochloride (Norimipramine) 是一种二苯并氮杂类衍生物三环类抗抑郁药,可作为选择性去甲肾上腺素再摄取抑制剂。 它还显示出较弱的 5-羟色胺再摄取抑制、α1 阻断、抗组胺和抗胆碱能作用。 | |||
T7341 |
Diclofensine
Ro 8-4650,(+/-)-双氮奋兴 |
Dopamine Receptor; Monoamine Transporter | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Diclofensine (Ro 8-4650) 是一种高效单胺再摄取抑制剂,在大鼠脑突触体中能够阻断多巴胺 (IC50=0.74 nM)、去甲肾上腺素 (IC50=2.3 nM) 和 5-羟色胺 (IC50=3.7 nM)。 | |||
T29534 |
ABT-925 fumarate dihydrate
ABT 925,LU201640,ABT925,ABT-925,BSF201640,DAT201 |
||
ABT-925 is a selective dopamine D3 receptor (DRD3) antagonist with an in vitro affinity approximately 100 times higher for dopamine D3 receptors than for D2 receptors. | |||
T1970 |
Gedatolisib
PF-05212384,PKI-587 |
PI3K; mTOR | PI3K/Akt/mTOR signaling |
Gedatolisib (PF-05212384) 是一种高效的双重 PI3Kα (IC50:0.4 nM),PI3Kγ (IC50:5.4 nM) 和 mTOR (IC50:1.6 nM)抑制剂。它在 mTOR 复合物mTORC1和mTORC2中同样有效。 | |||
T7747 |
Datelliptium chloride hydrochloride
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Datelliptium chloride hydrochloride 是一种衍生自玫瑰树碱的 DNA 嵌入剂,具有抗肿瘤活性。 | |||
T23631 |
Adatanserin
WY-50324,WY 50324,WAY SEB 324,WY50324 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Adatanserin (WY 50324) 是一种混合型 5-HT1A 受体部分激动剂,也是一种 5-HT2A 和 5-HT2C 受体拮抗剂,具有潜在的神经保护活性,可用于研究焦虑和抑郁症。 | |||
T39630 |
Zandatrigine
NBI-921352,XEN901 |
Sodium Channel | Membrane transporter/Ion channel |
Zandatrigine (NBI-921352) 是钠通道蛋白 8 型亚基 α 的阻断剂,可用于癫痫治疗的神经系统病理学研究。 | |||
T13110 |
Tedatioxetine hydrobromide
Lu AA 24530 hydrobromide |
Dopamine Receptor; 5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) 是一种血清素-去甲肾上腺素-多巴胺再摄取抑制剂 ,也是 5-HT2A、5-HT2C、5-HT3 和 α1A-肾上腺素能受体的拮抗剂,可用于治疗抑郁症和焦虑症。 | |||
T19668 |
Tiomolibdate diammonium
Ammonium molybdenum sulfide,Ammonium tetrathiomolybdate,NSC 286644,ATTM,四硫钼酸铵,Coprexa |
Others | Others |
Tiomolibdate diammonium (NSC-286644) 是超氧化物歧化酶 1 (SOD1) 的抑制剂,具有抗血管生成和抗肿瘤活性。 Tiomolibdate diammonium 抑制铜酶的活性,包括 SOD1 和 COX。 | |||
T5159 |
Olodaterol hydrochloride
BI-1744 HCl,盐酸奥达特罗,BI 1744 hydrochloride |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Olodaterol hydrochloride (BI-1744 HCl) 是一种长效的、选择性 β2-adrenoceptor(β2-AR) 激动剂 (EC50=0.1 nM;pKi= 9.14 for human β2-adrenoceptor),可用于慢性阻塞性肺疾病 (COPD) 和肺纤维化的研究。 | |||
T23445 |
Anxiolytic/nonsedative agent-1
TCS 1205 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Anxiolytic/nonsedative agent-1 (TCS 1205) 是一种有效的选择性 GABAA 激动剂。Anxiolytic/nonsedative agent-1 对牛脑膜中的 BzR 显示出明显的亲和力,对 α1β2γ2、α2β2γ2、α5β3γ2 的 Kis 分别为 14、121、239 nM。Anxiolytic/nonsedative agent-1 在体外表现出 α2 选择性功效,在体内表现出抗焦虑选择性作用。 | |||
T2189 |
Sodium orthovanadate
Sodium vanadate,钒酸钠,Trisodium vanadate,Sodium pervanadate |
ATPase; Phosphatase | Membrane transporter/Ion channel; Metabolism |
Sodium orthovanadate 是一种蛋白酪氨酸磷酸酶,碱性磷酸酶和一些ATP 酶的抑制剂,有可能充当磷酸盐类似物。它具有胰岛素样作用、对心室肌的正性肌力作用和其他代谢作用。 | |||
T34795 |
Tedatioxetine
Lu AA-24530,Lu AA24530,Lu AA 24530 |
||
Tetaxetine( LU AA24530) has been reported as a triple reuptake inhibitor (5-HT > NE > DA) and 5-HT2A, 5-HT2C, 5-HT3 and α1A-adrenergic receptor antagonist.Meanwhile, it is an antidepressant agent. | |||
T15378L |
Gemcitabine elaidate hydrochloride
CO-101 hydrochloride,Gemcitabine elaidate hydrochloride(210829-30-4(free base)),Gemcitabine 5'-elaidate hydrochloride,CP-4126 hydrochloride |
Others | Others |
Gemcitabine elaidate (CP-4126) hydrochloride 是 Gemcitabine 的亲脂性前药。Gemcitabine elaidate hydrochloride 通过酯酶转化为 Gemcitabine 以被磷酸化。Gemcitabine elaidate hydrochloride 可以口服给药,具有抗肿瘤活性。 | |||
T74398 |
DATPT
|
Reactive Oxygen Species; Antibacterial | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
DATPT 是一种小分子 12WLVSKF17 肽模拟分子。DATPT 抑制 SNX9-p47phox 相互作用,抑制活性氧和炎性细胞因子的产生。DATPT 具有抗炎和抗菌活性,通过减少 ATP 的产生发挥作用。DATPT 是治疗脓毒症的潜在化合物。 | |||
T29645 |
Adatanserin hydrochloride
WY50324 hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Adatanserin hydrochloride (WY50324 hydrochloride) 是一种新型 5-HT(1A)/5-HT(2) 受体配体,具有潜在的神经保护作用,抑制内源性氨基酸缺血性外排,可用于研究抑郁症和焦虑症。 | |||
T9901A-007 |
Datopotamab
|
Others | Others |
Datopotamab (CDP7657) 是一种靶向 TROP2 的抗体,是 Datopotamab deruxtecan 的裸抗,可用于合成抗体活性分子偶联物( Datopotamab deruxtecan)。 | |||
T22867 |
Indatraline hydrochloride
|
Others | Others |
Inhibits transporters for 5-HT (SERT), dopamine (DAT) and noradrenalin (NET) | |||
T38630 | Ludaterone | ||
Ludaterone is an antiandrogen agent, with potent antiandrogenic activity. | |||
T70323 | Diethanolamine Fusidate | ||
Diethanolamine Fusidate is a bacteriostatic antibiotic with similar activity and better absorption after oral administration (in animals) than the sodium salt of Fusidic Acid. This product inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA. | |||
T76875 | Zanidatamab | ||
Zanidatamab (ZW25) 是一种针对 2 个不同 HER2表位 (ECD2 和 ECD4) 的人源双特异性单克隆抗体。Zanidatamab 具有抗肿瘤活性。 | |||
T77104 | Obrindatamab | ||
Obrindatamab 是一种人源化抗 B7-H3/CD3双特异性抗体。Obrindatamab 结合 B7-H3和 CD3,从而介导针对表达 B7-H3的癌细胞的重定向细胞毒性 T 淋巴细胞 (CTL) 活性。Obrindatamab 可用于癌症研究。 | |||
T68661 |
Edatrexate
CGP 30694 |
||
Edatrexate (CGP 30694),即 10-乙基-10-去甲氨基蝶呤,是甲氨蝶呤Methotrexate 的类似物,对耐 MTX 肿瘤具有抗肿瘤活性。Edatrexate 是一种抗叶酸抗代谢物,可用于研究非小细胞肺癌,乳腺癌,非霍奇金淋巴瘤和头颈部癌症的研究。 | |||
T80434 |
Heteropodatoxin-2
|
Potassium Channel | Membrane transporter/Ion channel |
Heteropodatoxin-2为含30个氨基酸的肽,归属于异足毒素类。它能电压依赖性地阻断非洲爪蟾卵母细胞表达的Kv4.2电流,并在正电位较高时显示出较低的阻断效应。 | |||
T14339 |
Athidathion
GS-13006 |
Others | Others |
Thiophos (GS-13006) is an insecticide, which is an organic phosphate ester. | |||
T40670 |
7-Deaza-7-propargylamino-dATP
|
||
7-Deaza-7-propargylamino-dATP is a deoxyadenosine triphosphate (dATP) analog utilized in the field of gene sequencing. | |||
T38532 |
7-Deaza-7-propargylamino-ddATP
|
||
7-Deaza-7-propargylamino-ddATP, an analog of ddATP, serves as a viable option for gene sequencing purposes due to its chemical composition. | |||
T75026 | PROTAC TYK2 degradation agent1 | PROTACs | PROTAC |
PROTACTYK2 degradation agent1为亚型选择性TYK2降解剂,表现出杰出的TYK2降解活性,其DC50为14 nM,适用于自身免疫性疾病研究。 | |||
T24604 |
PDAT
Propyl Dimethyl Amino Tryptamine |
||
PDAT is a noncompetitive Indolethylamine N-methyltransferase inhibitor. | |||
T64510 | Hexan-3-yl carbonochloridate | ||
Hexan-3-yl carbonochloridate 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64510。 | |||
T20679 |
Pyridate
P1 3419,CL-11344,Fenpyrate,Pyron,CL11344,CL 11344 |
||
Pyridate is mainly used as a selective post seedling herbicide. | |||
T15378 |
Gemcitabine elaidate
Gemcitabine 5'-elaidate,反油酸吉西他滨,吉西他滨反油酸酯,Gemcitabine (elaidate),CO-101,CP-4126 |
Apoptosis; Nucleoside Antimetabolite/Analog; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Gemcitabine elaidate (CP-4126) 是 Gemcitabine 的亲脂性前药。它通过酯酶转化为 Gemcitabine 以被磷酸化。它具有抗肿瘤活性。 | |||
T10982 |
ddATP
2',3'-Dideoxyadenosine 5'-triphosphate |
Others | Others |
ddATP is a dideoxynucleotide, used as a chain extension inhibitor for DNA polymerase, and used for DNA sequencing by the Sanger method. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5165 |
10-Deacetyltaxol
10-DAT,10-Desacetyl Paclitaxel,去乙酰紫衫醇,Deacetyltaxol,10-去乙酰紫杉醇,10-deacetyl-paclitaxel,Deacetyl Paclitaxel |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
10-Deacetyltaxol (10-DAT) 是从红豆杉中分离得到的一种紫杉醇衍生物,对人脑胶质细胞瘤和神经母细胞瘤细胞具有细胞毒性。它能促进微管蛋白的聚合,在体外抑制由钙离子诱导的微管解聚。 | |||
TN6552 |
5,7-Dimethoxyluteolin
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
5,7-Dimethoxyluteolin 是 5,7-二甲基木犀草素的一种衍生物,可以活化多巴胺转运蛋白,EC50为 3.417 μM。 | |||
T3273 |
Bifendate
联苯双酯,Bifendatatum |
HBV; Reverse Transcriptase | Microbiology/Virology |
Bifendate (Bifendatatum) 是 Schisandrin C 的合成中间体,在慢性 B 型肝炎的研究中具有抗HBV 功效,用于治疗病毒性肝炎和药物性肝损伤引起的转氨酶升高。 | |||
TN3831 |
(-)-Denudatin B
Denudatin B |
ATPase; Potassium Channel; Calcium Channel; PAFR | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
(-)-Denudatin B (Denudatin B) 源自 Magnolia fargesii。 (-)-Denudatin B 通过抑制胶原蛋白和凝血酶诱导的磷酸肌醇分解,在高浓度下具有非特异性抗血小板作用。 | |||
T2736 |
Sodium Demethylcantharidate
Sodium norcantharidin,去甲斑蝥酸钠 |
Others; Endogenous Metabolite | Metabolism; Others |
Sodium Demethylcantharidate (Sodium norcantharidin) 是内源性代谢产物的一种。 | |||
T5735 |
Methyl deacetylasperulosidate
Deacetyl asperulosidic acid methyl ester,6α-Hydroxygeniposide,去乙酰车叶草苷酸甲酯 |
Others | Others |
Methyl deacetylasperulosidate (6α-Hydroxygeniposide) 是环烯醚萜类化合物,能够降低正常小鼠的血糖水平,对小鼠具有通便作用。 | |||
T3150 |
Caudatin
告达亭苷元,告达庭 |
Apoptosis; Others | Apoptosis; Others |
Caudatin 是白首乌中的一种甾体类天然产物,具有抗肿瘤和抗血管生成作用。它是一种 C-21 甾体糖苷,可使细胞周期停滞,诱导细胞凋亡。 | |||
T2938 |
(E/Z)-Polydatin
云杉新甙,(E/Z)-虎杖苷,Polydatin,(E/Z)-Piceid |
Phospholipase | Metabolism |
(E/Z)-Polydatin (Polydatin) 是从虎杖的根和根茎中分离得到的一种单晶化合物。它具有抗血小板聚集、心脏保护作用、抗低密度脂蛋白 (LDL) 氧化作用、抗炎和免疫调节功能。 | |||
T7958 |
Methyl arachidate
花生酸甲酯,Methyl Icosanoate |
Others; Aminopeptidase | Metabolism; Others |
Methyl arachidate (Methyl Icosanoate) 是一种天然化合物,具有白三烯 A4 水解酶 (LTA4H) 抑制活性。 | |||
T3427 |
Polydatin
Piceid,虎杖苷,Polydotin Peceid |
Apoptosis; Mitophagy; NF-κB; Autophagy | Apoptosis; Autophagy; NF-κB |
Polydatin (Piceid) 是从传统中药虎杖根中提取的一种天然产物,在多个实验模型中具有抗炎作用。它可抑制 G6PD,并诱导氧化和内质网应激。 | |||
TN3774 |
Daturametelin I
|
Others | Others |
Daturametelin I 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 TN3774,CAS号为 904667-65-8。 | |||
T38415 | Adenosine 5′-monophosphoramidate sodium | ||
Adenosine 5′-monophosphoramidate sodium is a derivative of adenosine used as an intermediate for nucleotide synthesis. It significantly influences the accumulation of cyclic AMP. | |||
T75637 | Demethylcantharidate disodium | ||
Demethylcantharidate disodium 是一种内源性代谢产物,能通过诱导内质网应激来促进肝癌细胞的凋亡,并且对多种类型的癌症展现出良好的抗癌活性。 | |||
TN3775 |
Daturataturin A aglycone
|
Others | Others |
Daturataturin A aglycone 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 TN3775,CAS号为 904665-71-0。 | |||
TN3772 | Datiscin | Others | Others |
Datiscin 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 TN3772,CAS号为 16310-92-2。 | |||
TN7002 |
Methyl linolelaidate
|
||
Methyl linolelaidate is a natural product. | |||
T3S0626 |
Denudatine
光翠雀碱;裸翠雀亭,光翠雀碱 |
Others | Others |
Denudatine 是分离自乌头属和翠雀属植物中,能够影响心室纤维的动作电位,并抑制乌头碱的致心律失常作用。 | |||
TN6570 |
Daturaolone
|
||
Daturaolone has potency in reducing the harmful effects or in maintaining the normal hepatic physiological mechanisms in both acute and chronic hepato-toxic induced liver damage in rats. Daturaolone also possesses in vivo anti-inflammatory and antinocicep | |||
TN3773 |
Daturabietatriene
|
Others | Others |
Daturabietatriene is a natural product from Pinus yunnanensis. | |||
TN3776 |
Daturataturin A
|
Others | Others |
Daturataturin A是一种天然产物,属于茄科曼陀罗属,其产品编号为 TN3776,CAS号为 133360-51-7。Daturataturin A可用作对照参考。 | |||
TN5218 |
Valerosidate
|
Others | Others |
Valerosidate is a natural product from Valeriana jatamansi. | |||
TN6027 |
Pedatisectine F
2-Methyl-6-(1,2,3,4-tetrahydroxybutyl)pyrazine |
||
Pedatisectine F是一种天然产物,属于天南星科半夏属,其产品编号为 TN6027,CAS号为 206757-32-6。Pedatisectine F可用作对照参考。 | |||
TN3262 |
8(17),12E,14-Labdatrien-20-oic acid
|
Others | Others |
8(17),12E,14-Labdatrien-20-oic acid is a natural product from Isodon yuennanensis. | |||
TN3788 |
Decursidate
|
Others | Others |
Decursidate是一种天然产物,属于伞形科前胡属,其产品编号为 TN3788,CAS号为 272122-56-2。Decursidate可用作对照参考。 | |||
TN2161 |
Rotundatin
|
Others | Others |
Rotundatin is a natural product from Dendrobium rotundatum. |