首页工具

登录

搜索结果

Search Results for " p-11 "

57

抑制剂 & 化合物

4

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T7554	Substance P (7-11) Substance P 7-11(TFA)	Others; Neurokinin receptor	GPCR/G Protein; Neuroscience; Others
	Substance P (7-11) (Substance P 7-11(TFA)) 是神经肽物质P 的C-末端片段，可引起细胞内钙浓度的增加。
TP1369L	[Sar9,Met(O2)11]-Substance P acetate [Sar9,Met(O2)11]-Substance P acetate(110880-55-2 free base)	Neurokinin receptor	GPCR/G Protein; Neuroscience
	[Sar9,Met(O2)11]-Substance P acetate(110880-55-2 free base) 是一种速激肽 NK1 受体选择性激动剂。它是一种选择性速激肽 NK1 受体激动剂。它和 septide（每只大鼠 10-100 pmol，i.c.v.）在增加平均动脉血压 (MAP) 和心率 (HR)，但它们的时间进程不同。两种激动剂都以剂量依赖性方式增加洗脸和吸鼻，而它是一种产生美容效果的化合物。
T7828	[Sar9,Met(O2)11]-Substance P Bhsar-sp,NA,精氨酰-脯氨酰-赖氨酰-脯氨酰-谷氨酰-谷氨酰-苯丙氨酰-苯丙氨酰-SAR-亮氨酸-蛋氨酸[O2]-胺	Neurokinin receptor	GPCR/G Protein; Neuroscience
	[Sar9,Met(O2)11]-Substance P (NA) 是选择性速激肽NK1受体激动剂。
T34081	Piromelatine NEU-P-11,NEU-P 11,NEU-P11	P2X Receptor; 5-HT Receptor; MT Receptor; Sodium Channel; TRP/TRPV Channel	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Piromelatine 是褪黑激素 MT1/MT2 受体、5-HT1A 和 5-HT1D 的激动剂，也是 5-HT2B 的拮抗剂。Piromelatine 具有抗痛觉活性，对 P2X3、TRPV1 和 Nav1.7 通道有抑制作用，可用于促进睡眠、缓解疼痛、抗神经退行性疾病和抗抑郁疾病的研究。
TP1879L1	P11 acetate	Integrin	Cytoskeletal Signaling
	P11 acetate 是一种整合素 αvβ3-玻连蛋白相互作用拮抗剂 (IC50 = 2.74 nM)。
TP1369	[Sar9,Met(O2)11]-Substance P TFA(110880-55-2,free) [Sar9,Met(O2)11]-Substance P TFA
	[Sar9,Met(O2)11]-Substance P TFA is a selective tachykinin NK1 receptor agonist.[Sar9,Met(O2)11]-Substance P and septide (10-100 pmol per rat, i.c.v.) are equipotent in increasing mean arterial blood pressure (MAP) and heart rate (HR), yet they have dissi
TP2352	Septide Substance P (6-11), pyroglutamyl(6)-proline(9)-,6-Glp-9-pro-substance P (6-11)
	Septide is an NK1 receptor agonist acting at a site distinct from substance P.
TP1879	HSDVHK-NH2 P11
	Potent antagonist of the integrin αvβ3-vitronectin interaction (IC50 = 25.72 nM). Blocks proliferation and induces apoptosis in HUVECs; antiangiogenic.
TP1831	[Nle11]-Substance P
	[Nle11]-Substance P is a substance P analog that avoids methionine oxidation problems. Substance P was found in the gut as well as in the brain. It is responsible for a number of excitatory effects on both central and peripheral neurons.
TP2326L	Oligopeptide P11-4 acetate Oligopeptide P11-4 acetate(593266-60-5 free base)	Others	Others
	Oligopeptide P11-4 acetate(593266-60-5 free base) 是一种肽。
T76455	Substance P (4-11)
	Substance P (4-11) 是 Substance P (Substance P ) 的 C 末端片段，是一种 Substance P 激动剂，对NK1受体具有高度选择性。
T76454	Substance P (5-11)
	Substance P (5-11) 是 Substance P (Substance P ) 的 C 端七肽，是一种神经肽，可以与NK-1速激肽受体结合。
T81078	Substance P (3-11)
	Substance P (3-11)，作为P 物质 (SP) 的片段肽，具备穿透血脑屏障的能力，且对豚鼠回肠显示出收缩活性。
T81079	Substance P (2-11)
	Substance P (2-11)为P物质（SP）片段肽，具有对豚鼠回肠产生收缩活性的特性。同时，Substance P (2-11)能够抑制3H SP在BBMEC单分子层中的渗透。
T76453	Substance P (6-11)
	Substance P (6-11)，Substance P 的C末端六肽酰胺，可与NK-1速激肽受体结合，展现出对运动神经元的去极化作用以及降压效应。
T76483	[Sar4] Substance P (4-11)
	[Sar4] Substance P (4-11)为Substance P (4-11)的类似物，后者是Substance P (Substance P) C端片段并充当Substance P激动剂。
T76447	[DAla4] Substance P (4-11)
	[DAla4] Substance P (4-11) 作为Substance P的衍生物，能够有效抑制125I-Bolton Hunter标记的Eledoisin（IC50值为0.5 μM）及125I-Bolton Hunter标记的Substance P (IC50值为0.15 μM)与大鼠大脑皮层膜之间的结合。
T76402	[Glp6] Substance P (6-11)
	[Glp6] Substance P (6-11)为Substance P (6-11)的一种类似物，主要通过激活大鼠膀胱中的“隔膜敏感”速激素受体，促进[3H]-单磷酸肌醇 ([3H]-IP1)的生成。
T76403	[Glp5] Substance P (5-11)
	[Glp5] Substance P (5-11)为一八肽，为大鼠中枢神经系统(CNS)主要P物质片段之一，局部调节大鼠纹状体多巴胺释放。
T76462	[Glp5,Sar9] Substance P (5-11)
	[Glp5,Sar9] Substance P (5-11) 是一种Substance P 的类似物。
T75769	[Sar9,Met(O2)11]-Substance P TFA
	[Sar9,Met(O2)11]-Substance P TFA 是一种选择性的速激肽NK1受体激动剂。
T83496	[D-Pro4,D-Trp7,9,10] Substance P (4-11)
	[D-Pro4,D-Trp7,9,10] Substance P (4-11) 是一种tachykinin拮抗剂，具有高效性。
T76404	[Glp5,(Me)Phe8,Sar9] Substance P (5-11)
	[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (DiMe-C7) 是一种 Substance P 类似物，在大鼠大脑中对神经激肽 1 受体 (NK1R) 的作用与 Substance P 大致相等，但作用时间大大延长。[Glp5,(Me)Phe8,Sar9] Substance P (5-11) 能选择性地激活大鼠大脑间脑和中脑皮层的多巴胺代谢。[Glp5,(Me)Phe8,Sar9] Substance P (5-11) 还可增加大鼠运动活性，诱导成瘾剂寻求行为的恢复。
T83495	[D-Pro4,D-Trp7,9] Substance P (4-11)
	[D-Pro4,D-Trp7,9]Substance P(4-11)为高效Substance P 拮抗剂，可降低血浆醛固酮(ALDO)浓度。
T76406	[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11)
	[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) 为高效的神经激肽 NK1 拮抗剂，能够有效抑制金蛋白 P 物质 (GPSP) 与 P 物质 (SP) 的活性。
TP1087	Substance P Neurokinin P,P物质	Endogenous Metabolite; Neurokinin receptor	GPCR/G Protein; Metabolism; Neuroscience
	Substance P (Neurokinin P) 是一种神经肽，其内源性受体是神经激肽1受体，在中枢神经系统中作为神经递质和神经调节剂。
TP1862L	[Sar9] Substance P acetate(77128-75-7 free base)	Neurokinin receptor	GPCR/G Protein; Neuroscience
	[Sar9] Substance P acetate(77128-75-7 free base) 是一种 NK-1 受体激动剂。 rNK1 特异性激动剂 [Sar-9,Met(O2)11]-SP 模拟了 SP 对孕酮代谢的作用。
T14765	BOS-172722	Kinesin	Cytoskeletal Signaling
	BOS-172722 是一种单极纺锤体 1 (MPS1) 检查点抑制剂，对MPS1 (1 mM ATP) 和P-MPS1 的IC50值分别为 11 nM 和 63 nM。它可研究多种乳腺癌。
T25122	Awl 60 Awl-60,Awl60,Tyr-pro-D-phe-phe-D-phe-D-trp-metnh2
	Awl 60 is a substance P (6-11) non-competitive antagonist.
T78069	RPR132595A hydrochloride NPC hydrochloride	Drug Metabolite	Metabolism
	RPR132595A (NPC) hydrochloride，CPT-11的活性代谢产物，由细胞色素P-450 3A4 (CYP3A4) 催化产生，经尿液排出体外。
TP1087L	Substance P acetate (87616-84-0 Free base)
	Substance P acetate (87616-84-0 Free base) 是一种十一肽（由11个氨基酸残基链组成的肽），属于速激肽神经肽家族。
T70456	Nolpitantium Free Base
	Nolpitantium Free Base is a highly selective nonpeptide antagonist of neurokinin-1 (NK1) receptor. Nolpitantium potently, selectively and competitively inhibited substance P binding to NK1 receptors from various animal species, including humans. In vitro, it was a potent antagonist in functional assays for NK1 receptors such as [Sar9, Met(O2)11]substance P-induced endothelium-dependent relaxation of rabbit pulmonary artery and contraction of guinea-pig ileum. Up to 1 mkM, Nolpitantium had no eff...
TP1932	[D-Trp7,9,10]-Substance P
	Substance P analog that inhibits activation of Gq/11 by M1 muscarinic ACh receptors. Does not inhibit Gi/o activation by M2 ACh receptors.
T73466	Pulixin
	Pulixin 阻碍了 FREP1 与恶性疟原虫感染细胞的裂解物的结合，防止传播至蚊子，其中EC50值为11 µM。同时，Pulixin 抑制无性期恶性疟原虫的增殖，EC50值达47 nM。
T60301	(Z)-p-cyano-α-Cyanostilbene
	(Z)-p-cyano-α-Cyanostilbene (compound 11) 是一种 phenantrene 衍生物，具有抗增殖活性。(Z)-p-cyano-α-Cyanostilbene 对 HeLa (IC50=0.21 μM) 和 HepG2 (IC50=0.230 μM) 细胞显示出显着的选择性，对正常皮肤成纤维细胞没有细胞毒性 (IC50>100 μM)。
T19553	RPR132595A NPC	Others	Others
	RPR132595A is an active CPT-11 metabolite, it is generated by cytochrome P-450 3A4 (CYP3A4).
T75726	ω-Conotoxin MVIIC TFA
	ω-Conotoxin MVIIC TFA 是一种阻断N和P/Q型钙通道(Ca2+ channel)的化合物，能显著抑制由11-keto-βboswellic acid介导的谷氨酸释放。
TP1862	[Sar9] Substance P
	[Sar9]-Substance P is one of NK-1 receptor agonist. The action of SP on progesterone metabolism was mimicked by the rNK1-specific agonist [Sar-9,Met(O2)11]-SP.
T29186	YM49598 YM-49598,YM 49598
	YM49598 is a tachykinin receptor antagonist. YM49598 exhibited high binding affinities at NK(1) (pK(i) = 9.09 +/- 0.02) and NK(2) (pK(i) = 9.94 +/- 0.03) receptors, respectively. YM49598 was almost inactive but produced a potent inhibition (IC(50) = 11 +/
TMIH-0002	(+/-)-Verapamil hydrochloride-d7
	(+/-)-Verapamil hydrochloride-d7 是 (+/-)-Verapamil hydrochloride 的氘代化合物。(+/-)-Verapamil hydrochloride 的 CAS 号为 152-11-4。Verapamil hydrochloride 是一种钙通道阻滞剂，是一种可口服的 P 糖蛋白 (P-gp) 抑制剂，可抑制CYP3A4，用于高血压、心律不齐和心绞痛的研究。
T62752	KRAS inhibitor-16
	KRAS inhibitor-16 (compound 3-11) 是一种 KRAS G12C 的有效抑制剂 (IC50: 0.457 μM)。KRAS inhibitor-16 在 MIA PaCA-2，A549 细胞中表现出 p-ERK 抑制作用，IC50s 分别为 3.06，11.1 μM。 KRAS inhibitor-16 具有潜力进行胰腺癌，结直肠癌和肺癌的研究。
T79438	c-Myc inhibitor 11	c-Myc	Cell Cycle/Checkpoint
	c-Myc inhibitor11（Compound 67e），一种c-MYC抑制剂（pEC50: 6.4），在大鼠药代动力学评估中表现出高清除率、中等体积分布和短半衰期，适用于癌症研究领域。
T35926	Bz-IEGR-pNA (acetate)
	Bz-IEGR-pNA is a colorimetric substrate for Factor Xa.1 Factor Xa preferentially binds to and cleaves the Ile-Glu-Gly-Arg (IEGR) peptide sequence to release p-nitroanilide (pNA), which can be quantified by colorimetric detection at 405 nm as a measure of Factor Xa activity.References1. Aruell, L., Friberger, P., Karlsson, G., et al. A new sensitive and highly specific chromogenic peptide substrate for factor Xa. Thromb. Res. 11(5), 595-609 (1977). Bz-IEGR-pNA is a colorimetric substrate for Fact...
T74600	Keap1-Nrf2-IN-9
	Keap1-Nrf2-IN-9（compound 11）是一种有效Keap1-Nrf2PPI抑制剂，IC50为0.575 µM。该化合物能够提升Nrf2靶基因表达，涉及血红素加氧酶1 (Hmox1)、谷胱甘肽S转移酶P (GstP) 以及谷氨酸-半胱氨酸连接酶的催化(Gclc)与调节(Gclm)亚基。在ARPE19细胞中，Keap1-Nrf2-IN-9展现出无细胞毒活性。
T35494	(±)11(12)-EET
	(±)11(12)-EET is a fully racemic version of the R/S enantiomeric forms biosynthesized from arachidonic acid by cytochrome P450 enzymes.[1][2][3[]A higher proportion of 11(R),12(S)-EET is produced by the CYP450 isoforms CYP2C23 and CYP2C24 while CYP2B2 produces a higher proportion of 11(S),12(R)-EET.[3]11(12)-EET has been shown, along with 8(9)-EET to play a role in the recovery of depleted calcium pools in cultured smooth muscle cells[4] It also inhibits basolateral 18-pS potassium channels in t...
T83947	HDAC4 CHDI Degrader 11
	HDAC4 CHDI Degrader 11是一种高效且选择性的HDAC4降解剂（PROTAC），其在Jurkat E6-1细胞和Jurkat细胞中的DC50值分别为4 nM和6 nM。该化合物由类IIa HDAC抑制剂三氟甲基噁二唑通过连接体与Von Hippel-Lindau (VHL) 蛋白的配体连接而成。在亨廷顿病小鼠细胞模型中，HDAC4 CHDI Degrader 11能强效地降解HDAC4（DC50= 1nM）。在神经母细胞瘤细胞系中，可与P-糖蛋白抑制剂Elacridar联用以实现更有效的降解。
T38220	11-cis Retinol
	11-cisRetinol is an isomer of vitamin A . It is formed from vitamin A,viaatrans-retinyl ester intermediate, by the enzyme RPE65 in the retinal pigment epithelium and then converted to 11-cis retinal as part of the visual cycle.1,211-cisRetinol is an agonist of salamander and human red rod opsins expressed in COS cells and an inverse agonist of salamander red cone opsin, as well as human red and green cone opsins expressed in COS cells.3It promotes pigment formation in cone, but not rod, photorec...
T35909	Penicinoline
	Penicinoline is an alkaloid that has been found in Penicillium and has antimalarial, insecticidal, and anticancer activities.1,2 It is active against chloroquine-sensitive and -resistant strains of P. falciparum (IC50 = 25 μM for both).1 Penicinoline (1,000 ppm) is also active against the aphid A. gossypii.2 It inhibits proliferation of 95-D and HepG2 cancer cells (IC50s = 0.57 and 6.5 μg/ml, respectively) but not HeLa, KB, KBv200, or Hep-2 cells (IC50s = >100 μg/ml). \|1. Naveen, B., Ommi, N.B.,...
T35700	FR901379
	FR901379 is an echinocandin-like antifungal lipopeptide.1 It is active against C. albicans, C. krusei, C. tropicalis, C. utilis, A. fumigatus, and A. niger fungi (IC50s = <0.003-1.9 μg/ml). FR901379 is protective against C. albicans infection in mice (ED50 = 1.1 mg/kg). It also reduces the number of pulmonary cysts and trophozoites in a mouse model of P. carinii infection. \|1. Fujie, A., Iwamoto, T., Sato, B., et al. FR131535, a novel water-soluble echinocandin-like lipopeptide: Synthesis and bi...
T37749	Benanomicin A
	Benanomicin A is a microbial metabolite that has been found inActinomycetesand has antifungal, fungicidal, and antiviral activities.1,2It is active against a variety of mammalian and plant pathogenic fungi, includingC. albicans,T. mentagrophytes,C. neoformans,P. oryzae, andA. niger(MICs = 3.13-50 μg/ml).1Benanomicin A inhibits HIV-1 viral infection in MT-4 cells in a concentration-dependent manner.2 1.Takeuchi, T., Hara, T., Naganawa, H., et al.New antifungal antibiotics, benanomicins A and B fr...

化合物

Substance P (7-11)

Cat.No: T7554

Synonym: Substance P 7-11(TFA)

Target: Others, Neurokinin receptor

[Sar9,Met(O2)11]-Substance P acetate

Cat.No: TP1369L

Synonym: [Sar9,Met(O2)11]-Substance P acetate(110880-55-2 free base)

Target: Neurokinin receptor

[Sar9,Met(O2)11]-Substance P

Cat.No: T7828

Synonym: Bhsar-sp,NA,精氨酰-脯氨酰-赖氨酰-脯氨酰-谷氨酰-谷氨酰-苯丙氨酰-苯丙氨酰-SAR-亮氨酸-蛋氨酸[O2]-胺

Target: Neurokinin receptor

Cat.No: T34081

Synonym: NEU-P-11,NEU-P 11,NEU-P11

Target: P2X Receptor, 5-HT Receptor, MT Receptor, Sodium Channel, TRP/TRPV Channel

Cat.No: TP1879L1

Target: Integrin

[Sar9,Met(O2)11]-Substance P TFA(110880-55-2,free)

Cat.No: TP1369

Synonym: [Sar9,Met(O2)11]-Substance P TFA

Cat.No: TP2352

Synonym: Substance P (6-11), pyroglutamyl(6)-proline(9)-,6-Glp-9-pro-substance P (6-11)

Cat.No: TP1879

Synonym: P11

[Nle11]-Substance P

Cat.No: TP1831

Oligopeptide P11-4 acetate

Cat.No: TP2326L

Synonym: Oligopeptide P11-4 acetate(593266-60-5 free base)

Target: Others

Substance P (4-11)

Cat.No: T76455

Substance P (5-11)

Cat.No: T76454

Substance P (3-11)

Cat.No: T81078

Substance P (2-11)

Cat.No: T81079

Substance P (6-11)

Cat.No: T76453

[Sar4] Substance P (4-11)

Cat.No: T76483

[DAla4] Substance P (4-11)

Cat.No: T76447

[Glp6] Substance P (6-11)

Cat.No: T76402

[Glp5] Substance P (5-11)

Cat.No: T76403

[Glp5,Sar9] Substance P (5-11)

Cat.No: T76462

[Sar9,Met(O2)11]-Substance P TFA

Cat.No: T75769

[D-Pro4,D-Trp7,9,10] Substance P (4-11)

Cat.No: T83496

[Glp5,(Me)Phe8,Sar9] Substance P (5-11)

Cat.No: T76404

[D-Pro4,D-Trp7,9] Substance P (4-11)

Cat.No: T83495

[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11)

Cat.No: T76406

Cat.No: TP1087

Synonym: Neurokinin P,P物质

Target: Endogenous Metabolite, Neurokinin receptor

[Sar9] Substance P acetate(77128-75-7 free base)

Cat.No: TP1862L

Target: Neurokinin receptor

Cat.No: T14765

Target: Kinesin

Cat.No: T25122

Synonym: Awl-60,Awl60,Tyr-pro-D-phe-phe-D-phe-D-trp-metnh2

RPR132595A hydrochloride

Cat.No: T78069

Synonym: NPC hydrochloride

Target: Drug Metabolite

Substance P acetate (87616-84-0 Free base)

Cat.No: TP1087L

Nolpitantium Free Base

Cat.No: T70456

[D-Trp7,9,10]-Substance P

Cat.No: TP1932

Cat.No: T73466

(Z)-p-cyano-α-Cyanostilbene

Cat.No: T60301

Cat.No: T19553

Synonym: NPC

Target: Others

ω-Conotoxin MVIIC TFA

Cat.No: T75726

[Sar9] Substance P

Cat.No: TP1862

Cat.No: T29186

Synonym: YM-49598,YM 49598

(+/-)-Verapamil hydrochloride-d7

Cat.No: TMIH-0002

KRAS inhibitor-16

Cat.No: T62752

c-Myc inhibitor 11

Cat.No: T79438

Target: c-Myc

Bz-IEGR-pNA (acetate)

Cat.No: T35926

Keap1-Nrf2-IN-9

Cat.No: T74600

Cat.No: T35494

HDAC4 CHDI Degrader 11

Cat.No: T83947

Cat.No: T38220

Cat.No: T35909

Cat.No: T35700

Cat.No: T37749

Cat. No.	Product Name	Target	Signaling Pathways
T37690	Phenylpyropene A
	Phenylpyropene A is a fungal metabolite originally isolated from P. griseofulvum that has enzyme inhibitory and insecticidal activities.1,2,3 It inhibits acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 0.8 μM).1 Phenylpyropene A inhibits diacylglycerol acyltransferase (DGAT) in rat liver microsomes (IC50 = 78.7 μM). It induces mortality in 100% of M. persicae when used at a concentration of 5 ppm.3 \|1. Kwon, O.E., Rho, M.C., Song, H.Y., et al. Phenylpyropene A and B, new inhibitors of ...
T36179	Aspulvinone O
	Aspulvinone O is a fungal metabolite that has been found in P. variotti and has antioxidant and anticancer activities.1,2 It scavenges 2,2-diphenyl-1-picrylhydrazyl radicals in a cell-free assay (IC50 = 11.6 μM).1 Aspulvinone O inhibits aspartate transaminase 1 (GOT1; Kd = 3.32 μM) and is cytotoxic to PANC-1, AsPC-1, and SW1990 pancreatic cancer cells (IC50s = 20.54-26.8 μM).2 It reduces the oxygen consumption rate (OCR) and induces apoptosis in SW1990 cells. Aspulvinone O (2.5 and 5 mg/kg) redu...
T36000	3-Hydroxyterphenyllin
	3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi...
T35624	Ajoene
	Ajoene is a disulfide that has been found inA. sativumand has diverse biological activities, including antibacterial, anticancer, antiplatelet, and antioxidant properties.1,2,3,4It is active against Gram-positive (MICs = 5-160 &#181g/ml) and Gram-negative bacteria (MICs = 136-200 &#181g/ml), as well as yeasts (MICs = 10-20 &#181g/ml).1Ajoene is cytotoxic to mouse melanoma cells (IC50= 18 &#181M), as well as human colon, lung, mammary, and pancreatic cancer cells (IC50s = 7-41 &#181M).2It reduces...

天然产物

Phenylpyropene A

Cat.No: T37690

Cat.No: T36179

3-Hydroxyterphenyllin

Cat.No: T36000

Cat.No: T35624

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼