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16

抑制剂 & 化合物

2

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T30935	ci-IP3/PM
	CI-IP3 /PM is a cell-permeable caged inositol triphosphate that promotes the release of Ca2+ from internal storage under UV photolysis.
T19266	Ins(1,4,5)-P3 hexapotassium salt 1,4,5-IP3 hexapotassium salt,D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt	Others	Others
	D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt is promotes endoplasmic The second messenger of net calcium ions.
T8867	RO2959 Hydrochloride RO2959 HCl	IL Receptor; Calcium Channel; Interleukin	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
	RO2959 Hydrochloride (RO2959 HCl) 是选择性CRAC 通道抑制剂，IC50为 402 nM。它是人IL-2产生的有效抑制剂，有效阻断 T 细胞受体触发的基因表达和 T 细胞功能途径。它是由Orai1/Stim1通道介导的钙存储进入的有效阻滞剂，IC50为 25 nM。
T41181	iP300v
	iP300v is a negative control for iP300w
T68759	OSIP339391
	OSIP339391 is a A2BAR antagonist.
T83733	TIP39 (human, bovine) TFA Tuberoinfundibular Peptide of 39 Residues
	TIP39作为一种神经肽及甲状旁腺激素受体2型(PTH2R)激动剂，在表达重组人或大鼠PTH2R的COS-7细胞中诱导cAMP积累（EC50分别为0.5和0.8 nM），以及在内源性表达PTH2R的F-11细胞中（EC50 = 1.15 nM）。在CFK2大鼠软骨细胞中，TIP39 (1 nM)诱导细胞周期在G0/G1阶段停滞，并减少软骨分化的主要调控因子Sox9的表达。此外，TIP39 (100 pmol/动物)在小鼠强迫游泳测试中减少了不动时间。
T4693	2-Aminoethyl diphenylborinate 2-Aminoethoxydiphenyl borate,二苯基酸,2-APB	Calcium Channel; TRP/TRPV Channel	Membrane transporter/Ion channel; Metabolism
	2-Aminoethyl diphenylborinate (2-APB) 是细胞通透性的 IP3R 和 TRP 通道抑制剂，还抑制 store-operated Ca2+(SOC)通道。
T9031	MCU-i4	Others; Mitochondrial Metabolism	Metabolism; Others
	MCU-i4 阻断IP3依赖的线粒体 Ca2+的摄取，是一种新型 MCU 负调节剂，可结合 MICU1 并损害肌肉细胞生长。
T11137	(E)-GABAB receptor antagonist 1	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	(E)-GABAB receptor antagonist 1 是 GABAB receptor antagonist 1 的反式结构。(E)-GABAB receptor antagonist 1 降低 GABA 诱导的 IP3 (三磷酸肌醇) 产生，IC50 为 37.9 μM。GABAB receptor antagonist 1是选择性的 GABAB (γ-氨基丁酸) 受体的负变构调节剂。
T83950	ARN 11391
	ARN 11391是ITPR1 (Inositol 1,4,5-trisphosphate (IP3) receptor type 1)的增效剂，它直接作用于ITPR1，从而增强细胞内钙离子信号。ARN 11391还能增强表达突变型ITPR1细胞中的钙信号，这与SCA29型脊髓小脑共济失调有关。
T11350	GABAB receptor antagonist 1	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	(E)-GABAB receptor antagonist 1 decreases GABA-induced IP3 (inositol trisphosphate) production with IC50 of 37.9 μM.GABAB receptor antagonist 1 is a selective and negative allosteric modulator of GABAB (γ-Aminobutyric acid) receptors.
T14202	AM-4668	GPR	Endocrinology/Hormones; GPCR/G Protein
	AM-4668 is a type 2 diabetes GPR40 agonist. For GPR40, in A9 cells (GPR40 IP3 assay) and CHO cells (GPR40 aequorin assay), the EC50s are 3.6 nM and 36 nM, respectively.
TP1710	Calmodulin Binding Peptide 1
	Calmodulin Binding Peptide 1, a potent CaM-binding peptide with picomolar (pM) affinity, originates from smooth muscle myosin light-chain kinase (MLCK peptide). It effectively blocks inositol trisphosphate (IP3)-induced calcium (Ca2+) release [1].
T14553	BHPI	Others	Others
	BHPI is a potent inhibitor of nuclear estrogen–ERα-regulated gene expression. Elicits sustained ERα-dependent activation of the endoplasmic reticulum (EnR) stress sensor, the unfolded protein response (UPR), and persistent inhibition of protein synthesis.
T36937	PtdIns-(1,2-dioctanoyl) (sodium salt)
	The phosphatidylinositol (PtdIns) phosphates represent a small percentage of total membrane phospholipids. However, they play a critical role in the generation and transmission of cellular signals. PtdIns-(1,2-dioctanoyl) is a synthetic analog of natural phosphatidylinositol (PtdIns) containing C8:0 fatty acids at the sn-1 and sn-2 positions. The compound features the same inositol and diacyl glycerol (DAG) stereochemistry as that of the natural compound. The short fatty acid chains of this anal...
T37030	PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt) PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt)
	The phosphatidylinositol (PtdIns) phosphates represent a small percentage of total membrane phospholipids. However, they play a critical role in the generation and transmission of cellular signals. PtdIns-(4)-P1 (1,2-dioctanoyl) is a synthetic analog of natural phosphatidylinositol (PtdIns) featuring C8:0 fatty acids at the sn-1 and sn-2 positions. The compound contains the same inositol and diacylglycerol (DAG) stereochemistry as the natural compound. PtdIns-(4)-P1 can be phosphorylated to di- ...

化合物

Cat.No: T30935

Ins(1,4,5)-P3 hexapotassium salt

Cat.No: T19266

Synonym: 1,4,5-IP3 hexapotassium salt,D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt

Target: Others

RO2959 Hydrochloride

Cat.No: T8867

Synonym: RO2959 HCl

Target: IL Receptor, Calcium Channel, Interleukin

Cat.No: T41181

Cat.No: T68759

TIP39 (human, bovine) TFA

Cat.No: T83733

Synonym: Tuberoinfundibular Peptide of 39 Residues

2-Aminoethyl diphenylborinate

Cat.No: T4693

Synonym: 2-Aminoethoxydiphenyl borate,二苯基酸,2-APB

Target: Calcium Channel, TRP/TRPV Channel

Cat.No: T9031

Target: Others, Mitochondrial Metabolism

(E)-GABAB receptor antagonist 1

Cat.No: T11137

Target: GABA Receptor

Cat.No: T83950

GABAB receptor antagonist 1

Cat.No: T11350

Target: GABA Receptor

Cat.No: T14202

Target: GPR

Calmodulin Binding Peptide 1

Cat.No: TP1710

Cat.No: T14553

Target: Others

PtdIns-(1,2-dioctanoyl) (sodium salt)

Cat.No: T36937

PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt)

Cat.No: T37030

Synonym: PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt)

Cat. No.	Product Name	Target	Signaling Pathways
T7190	Actein	Apoptosis; Akt; JNK; Autophagy	Apoptosis; Autophagy; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling
	Actein 是从升麻的根茎中分离的一种三萜糖苷，通过促进ROS/JNK 活化和钝化人膀胱癌中的AKT 途径来抑制细胞增殖，诱导自噬和凋亡。
T23538	Xestospongin C (-)-Xestospongin C	Others	Others
	IP3-dependent Ca2+ release inhibitor

天然产物

Cat.No: T7190

Target: Apoptosis, Akt, JNK, Autophagy

Cat.No: T23538

Synonym: (-)-Xestospongin C

Target: Others

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