19
9
Cat. No. | Product Name | Target | Signaling Pathways |
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T7440 |
p,p'-DDE
p,p'-dichlorodiphenyldichloroethylene,4,4'-DDE,Dichlorodiphenyldichloroethylene,2,2-双(4-氯苯基)-1,1-二氯乙烯 |
Androgen Receptor; Drug Metabolite | Endocrinology/Hormones; Metabolism |
p,p'-DDE (p,p'-dichlorodiphenyldichloroethylene) 是持久性 DDT 的主要代谢物。4,4'-DDE 是一种有效的雄激素受体拮抗剂,IC50=5 μM,Ki=3.5 μM。 | |||
T19739 |
Simazine
Tafazine,Aquazine,Radocon,Herbex,西玛津 |
Others | Others |
Simazine (Tafazine) 是三嗪类除草剂,普遍用于农业、盆栽植物和树木的生产。它具有植物毒性,但对土壤微生物和藻类毒性较低。 | |||
T12360 |
para-Nitroblebbistatin
p-Nitroblebbistatin |
Myosin | Cytoskeletal Signaling |
para-Nitroblebbistatin (p-Nitroblebbistatin) 是无细胞毒性、无荧光、光稳定、特异性的肌球蛋白 II (Myosin II) 抑制剂。para-Nitroblebbistatin 可用于肌球蛋白 II 在生理学、发育和细胞生物学中特殊作用的相关研究。 | |||
T39252L |
5-[(1S,2S)-2-[(Cyclopropylmethyl)amino]cyclopropyl]-N-(tetrahydro-2H-pyran-4-yl)thiophene-3-carboxamide hydrochloride
|
Others | Others |
5-[(1S,2S)-2-[(Cyclopropylmethyl)amino]cyclopropyl]-N-(tetrahydro-2H-pyran-4-yl)thiophene-3-carboxamide hydrochloride 是一种环丙酶化合物,可作为赖氨酸特异性脱甲基酶-1抑制剂,可用于精神分裂症、发育障碍和神经退行性疾病。 | |||
T0976 |
Propoxur
残杀威,Aprocarb,Propoxure,Baygon |
AChR; Antifungal | Microbiology/Virology; Neuroscience |
Propoxur (Propoxure) 是一种氨基甲酸酯类杀虫剂,用于控制蟑螂、苍蝇、蚊子以及草坪和草坪昆虫。 | |||
T34949 |
Trimethylolpropane caprate
UNII-X307CM75YF,Trimethylolpropane tridecanoate,Trimethylolpropane tricaprate |
||
Trimethylolpropane caprate has developmental toxicity in Sprague-Dawley rats. | |||
T12640 |
(R,R)-Glycopyrrolate
(R,R)-格隆溴铵,(R,R)-Glycopyrronium bromide,(R,R)-Glycopyrrolate bromide |
Others | Others |
(R,R)-Glycopyrrolate is an agent of anticholinergic, has the ability to reduce the frequency of drooling in vivo with developmental disabilities. | |||
T14963 |
CI-943
(±)-CI-943 |
Others | Others |
CI-943是一种新型潜在的抗精神病药物,它不与多巴胺(DA)受体结合,有一定的发育性神经毒性。 | |||
T61592 | Thalidomide-piperazine hydrochloride | ||
Thalidomide-piperazine hydrochloride is a chemical compound with potential applications in the research of leprosy and multiple myeloma. It serves as a valuable tool in developmental biology, facilitating significant discoveries in the biochemical pathways of limb development [1]. | |||
T29886 |
Almestrone
BA-38372,BA 38372,Ciba-38372,BA38372,Ciba 38372 |
||
Almestrone (developmental code names Ba 38372, Ciba 38372), also known as 7α-methylestrone, is a synthetic, steroidal estrogen which was synthesized in 1967 but was never marketed. It is used as a precursor in the synthesis of several highly active steroi | |||
T36092 |
Fenobucarb
|
||
Fenobucarb, a widely employed carbamate insecticide, poses potential risks to the cardiovascular and cerebrovascular systems in animals[1][2]. It triggers developmental neurotoxicity in zebrafish by engaging pathways related to inflammation, oxidative stress, degeneration, and apoptosis. | |||
T31123 |
cvxIAA
convex IAA,5-(3-MeOPh)-IAA |
||
cvxIAA is an orthogonal auxin-TIR1 receptor pair. cvxIAA triggers auxin signaling without interfering with endogenous auxin or TIR1/AFBs. cvxIAA hijacked the downstream auxin signaling in vivo both at the transcriptomic level and in specific developmental | |||
T82900 |
Bemfivastatin hemicalcium
PPD 10558 hemicalcium |
||
Bemfivastatin (PPD 10558) hemicalcium 作为口服HMG-CoA还原酶抑制剂,具备有效的降脂作用并能增强肝脏提取活性。该化合物的未观察到不良反应水平(NOAEL)在大鼠发育毒性研究中超过320 mg/kg/d,在家兔母体毒性及发育毒性研究中分别超过12.5 mg/kg/d和25 mg/kg/d。Bemfivastatin hemicalcium 适用于对他汀类药物不耐受且患有他汀相关性高胆固醇血症性肌痛的研究。 | |||
T81027 |
TCRS-417
T417 |
||
TCRS-417(T417)是一种对PBX1与其同源DNA靶序列界面进行对接的小分子化合物,能够有效干扰PBX1-DNA相互作用。它适用于癌症、发育障碍、炎症性病症、自身免疫性疾病及神经退行性疾病研究领域。 | |||
T69717 |
Dimethandrolone
|
||
Dimethandrolone (DMA), also known by its developmental code name CDB-1321, is an experimental androgen/anabolic steroid (AAS) and progestogen medication which is under investigation for potential clinical use. Dimethandrolone is an AAS, and hence is an agonist of the androgen receptor, the biological target of androgens like testosterone. It is also a progestin, or a synthetic progestogen, and hence is an agonist of the progesterone receptor, the biological target of progestogens like progestero... | |||
T37954 |
Sphingosine (d20:1)
Sphingosine (d20:1) |
||
Sphingosines are long-chain base precursors of cellular sphingolipids used directly in the synthesis of ceramide, which in combination with sialic acid forms ganglioside. Sphingosine can exist in four stereoisomers, however only sphingosine occurs naturally. Compared to other sphingolipids throughout the body, which are predominantly composed of C-18 sphingosine, only central nervous system (CNS) gangliosides contain significant amounts of sphingosine. The concentration of sphingosine within mam... | |||
T71911 |
CGP-11130 HCl
|
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4-Fluorophenibut (developmental code name CGP-11130; also known as β-(4-fluorophenyl)-γ-aminobutyric acid or β-(4-fluorophenyl)-GABA) is a GABAB receptor agonist which was never marketed. It is selective for the GABAB receptor over the GABAA receptor (IC50 = 1.70 μM and > 100 μM, respectively). The drug is a GABA analogue and is closely related to baclofen (β-(4-chlorophenyl)-GABA), tolibut (β-(4-methylphenyl)-GABA), and phenibut (β-phenyl-GABA). It is less potent as a GABAB receptor agonist t... | |||
T38269 | Purfalcamine | ||
Purfalcamine is an orally active, selective Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1) inhibitor with an IC50 of 17 nM and an EC50 of 230 nM. Purfalcamine has antimalarial activity and causes malaria parasites developmental arrest at the schizont stage[1][2]. Purfalcamine has low activity against Toxoplasma gondii calcium-dependent protein kinase 3 (TgCDPK3)[1]. Purfalcamine (225, 450 nM) has no effect on the parasitemia in the first 32 hours. After about 40 hours, paras... | |||
T83771 |
6-PPD
Antioxidant 4020,N-(1,3-Dimethylbutyl)-N′-phenyl-p-phenylenediamine |
||
6-PPD是一种取代的p-苯二胺。它通过形成亚硝基自由基来清除臭氧。当6-PPD的浓度分别为0.022 mg/L和0.22 mg/L时,斑马鱼胚胎的孵化能力分别下降了25.6%和78.9%。6-PPD还会降低斑马鱼胚胎的活动能力和体长,并诱导发育畸形及氧化应激。含有6-PPD的配方已作为橡胶中的稳定剂添加物和抗臭氧剂使用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN3910 |
Ecdysone
|
Apoptosis; ATPase; Glucocorticoid Receptor; Potassium Channel; Sodium Channel; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Endocrinology/Hormones; Membrane transporter/Ion channel; Metabolism |
Ecdysone 是存在于昆虫和草药中的主要类固醇激素,可以激活盐皮质激素受体并诱导细胞凋亡。Ecdysone 的活性代谢物 20-羟基蜕皮激素在协调发育过渡和体内稳态睡眠调节中起重要作用。 | |||
T7913 |
2-Bromobiphenyl
|
Others | Others |
2-Bromobiphenyl 是一种持久性有机污染物,主要存在于土壤和水中。它是一种已知的人类致癌物,与生殖和发育毒性等多种健康影响有关。 | |||
T5061 |
Lumichrome
7,8-Dimethylalloxazine,光色素 |
Others | Others |
Lumichrome (7,8-Dimethylalloxazine) 是人类体内的内源性化合物,由核黄素光降解产生。它利用 p53 依赖机制抑制人肺癌细胞生长并诱导凋亡。 | |||
T6368 |
Abscisic Acid
Abscisin II,Dormin,(+)-脱落酸,(+)-ABA,Abscisic Acid (Dormin) |
Others; Proton pump; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Others |
Abscisic Acid (Dormin) 是具有口服活性的植物激素,存在于蔬菜和水果中,也是内源性的哺乳动物激素。它是生长抑制剂,可以调节植物生长发育。他抑制质子泵,并导致 Ca2+依赖性的质膜去极化。它是 LANCL2 的天然配体,属于胰岛素敏感化合物,在糖尿病前期,2 型糖尿病和代谢综合征的研究中具有价值。 | |||
T5623 |
Bisphenol A
|
Others; Endogenous Metabolite | Metabolism; Others |
Bisphenol A 是酚类内源性代谢合成物,广泛用于环氧树脂和聚碳酸酯塑料的生产。它是生殖、发育和全身毒性物质,常被归类为内分泌干扰物。它与许多疾病有关,包括呼吸系统疾病、心血管疾病、糖尿病、肾脏疾病、肥胖和生殖障碍。 | |||
T4867 |
Erucic acid
Prifac 2990,芥酸,13(Z)-Docosenoic Acid,cis-13-docosenoic acid |
PI3K; Endogenous Metabolite | Metabolism; PI3K/Akt/mTOR signaling |
Erucic acid (13(Z)-Docosenoic Acid) 是单不饱和脂肪酸,分离自萝卜的种子。Erucic acid 可以容易地穿过血脑屏障,使大脑中长链脂肪酸的积累正常化。Erucic acid 能够改善认知障碍并有效预防痴呆。 | |||
T3746 |
Dimethyl phthalate
邻苯二甲酸二甲酯,Solvanom,Avolin,Fermine,避蚊酯 |
Others | Others |
Dimethyl phthalate (Fermine) 是一种邻苯二甲酸酯 (PAEs),是一种已知的内分泌干扰物,也是一种普遍存在的污染物。它常作为增塑剂,赋予硬质聚氯乙烯 (PVC) 树脂以柔韧性。 | |||
T4716 |
Pyrrole-2-carboxylic acid
吡咯-2-羧酸,2-Pyrrolecarboxylic acid,Minaline |
Endogenous Metabolite | Metabolism |
Pyrrole-2-carboxylic acid (Minaline) 是一种天然生物碱类,从海洋细菌Pelomonas puraquaesp. Nov 中分离得到。 | |||
T4776 |
Glycerol
Glycerin,甘油 |
Endogenous Metabolite | Metabolism |
Glycerol 是甘油三酯(即脂肪和油)和磷脂的重要成分。它在食品工业中被广泛用作甜味剂和保湿剂以及药物制剂。 |