Gambogenic acid

中文名称:新藤黄酸

Gambogenic Acid, identified from Gamboge, is an inhibitor of the FGFR signaling pathway in erlotinib-resistant non-small-cell lung cancer (NSCLC) and exhibits anti-tumor effects. Gambogenic acid acts is also an effective inhibitor of EZH2 that specifically and covalently binds to Cys668 within the EZH2-SET domain, and triggers EZH2 ubiquitination.

Gambogenic acid Chemical Structure

Gambogenic acid Chemical Structure

CAS: 173932-75-7

规格 价格 库存 购买数量
1mg 794.46 现货
10mg 5487.3 现货
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400-668-6834

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PI3K抑制剂选择性比较

抑制剂名称 引文数量 PI3K p110α p110β p110δ p110γ C2β Vps34 其他靶点
Dactolisib (BEZ235) 485 mTOR (p70S6K),ATR
Pictilisib (GDC-0941) 420 mTOR
LY294002 1610 CK2,DNA-PK
Idelalisib (CAL-101) 277
Buparlisib (BKM120) 277 mTOR
PI-103 100 DNA-PK,mTOR
NU7441 (KU-57788) 280 DNA-PK,mTOR
TGX-221 97
IC-87114 43
Wortmannin 323 DNA-PK,ATM,MLCK
XL147 analogue 11
ZSTK474 83
Alpelisib (BYL719) 215
AS-605240 35
PIK-75 HCl 44 DNA-PK
3-MA (3-Methyladenine) 889 Autophagy
A66 53 PI4Kβ
Voxtalisib (XL765) Analogue 6 DNA-PK,mTOR
Omipalisib (GSK2126458) 56 mTORC1,mTORC2
PIK-90 28
PF-04691502 49 P-Akt (S473),P-Akt (T308),mTOR
AZD6482 27 DNA-PK
Apitolisib (GDC-0980) 33 mTOR
GSK1059615 14 mTOR
Duvelisib (IPI-145) 48
Gedatolisib (PKI-587) 29 mTOR
TG100-115 14
AS-252424 21 Casein Kinase 2
NU7026 64 DNA-PK
BGT226 (NVP-BGT226) maleate 10 mTOR
Fimepinostat (CUDC-907) 35 HDAC1,HDAC3,HDAC10
PIK-294 2
AS-604850 10
Copanlisib 50
YM201636 16 PIKfyve
CH5132799 3
PIK-293 0
PKI-402 6 mTOR
TG100713 3
VS-5584 (SB2343) 15 mTOR
KU-0060648 11 DNA-PK
Taselisib (GDC 0032) 38
CZC24832 15
PI3K/mTOR Inhibitor-2 0 mTOR
IHMT-PI3Kδ-372 0
Parsaclisib (INCB050465) 0
Zandelisib 0
P110δ-IN-1 0
Inavolisib (GDC-0077) 4
SRX3207 0 Syk,BRD42,BRD41
GNE-477 1 mTOR
Selective PI3Kδ Inhibitor 1 (compound 7n) 2
acalisib (GS-9820) 1
leniolisib (CDZ 173) 1 DNA-PK
Bimiralisib (PQR309) 5 mTOR
Seletalisib (UCB-5857) 1
Tenalisib 0
IPI-3063 0
Autophinib 9 Autophagy
Eganelisib (IPI-549) 24
Serabelisib (TAK-117) 3
SF2523 3 DNA-PK,BRD4,mTOR
GDC-0326 2
SAR405 37
umbralisib (TGR-1202) 6
VPS34 inhibitor 1 (Compound 19) 8
Paxalisib (GDC-0084) 3 mTOR
AZD8835 3
Nemiralisib 5
PIK-III 21
VPS34-IN1 30
Voxtalisib (XL765) 14 DNA-PK,mTOR
AMG319 5
AZD8186 18
PF-4989216 1
Pilaralisib (XL147) 14
PI-3065 2
HS-173 20
Quercetin 45 PKC,Src,Sirtuin
Quercetin Dihydrate 9 SIRT1
GSK2636771 18
CAY10505 1
α-Linolenic acid 0
(E)-Akt inhibitor-IV 1
PIK-108 0
SPP-86 0
Resibufogenin 2 cyclin D1,Bax/Bcl-2,Caspase-8
Cinobufagin 0 caspase-9,Bcl-2,Akt
Trigonelline 1 microtubule,Akt,PLCγ1
Ailanthone 1 Akt,CDK,ATM/ATR
MTX-211 2 EGFR
Oroxin B 3 PTEN,Akt,COX-2
Deguelin 4 Akt
Samotolisib (LY3023414) 11 mTOR kinase,DNA-PK
GSK2292767 0
GNE-317 2
点击展开更多
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

产品质控

批次: S903104 DMSO]100 mg/mL]false]]]false]]]false 纯度: 99.94%
99.94

Gambogenic acid相关产品

相关信号通路图

PI3K抑制剂选择性比较

抑制剂名称 引文数量 PI3K p110α p110β p110δ p110γ C2β Vps34 其他靶点
Dactolisib (BEZ235) 485 mTOR (p70S6K),ATR
Pictilisib (GDC-0941) 420 mTOR
LY294002 1610 CK2,DNA-PK
Idelalisib (CAL-101) 277
Buparlisib (BKM120) 277 mTOR
PI-103 100 DNA-PK,mTOR
NU7441 (KU-57788) 280 DNA-PK,mTOR
TGX-221 97
IC-87114 43
Wortmannin 323 DNA-PK,ATM,MLCK
XL147 analogue 11
ZSTK474 83
Alpelisib (BYL719) 215
AS-605240 35
PIK-75 HCl 44 DNA-PK
3-MA (3-Methyladenine) 889 Autophagy
A66 53 PI4Kβ
Voxtalisib (XL765) Analogue 6 DNA-PK,mTOR
Omipalisib (GSK2126458) 56 mTORC1,mTORC2
PIK-90 28
PF-04691502 49 P-Akt (S473),P-Akt (T308),mTOR
AZD6482 27 DNA-PK
Apitolisib (GDC-0980) 33 mTOR
GSK1059615 14 mTOR
Duvelisib (IPI-145) 48
Gedatolisib (PKI-587) 29 mTOR
TG100-115 14
AS-252424 21 Casein Kinase 2
NU7026 64 DNA-PK
BGT226 (NVP-BGT226) maleate 10 mTOR
Fimepinostat (CUDC-907) 35 HDAC1,HDAC3,HDAC10
PIK-294 2
AS-604850 10
Copanlisib 50
YM201636 16 PIKfyve
CH5132799 3
PIK-293 0
PKI-402 6 mTOR
TG100713 3
VS-5584 (SB2343) 15 mTOR
KU-0060648 11 DNA-PK
Taselisib (GDC 0032) 38
CZC24832 15
PI3K/mTOR Inhibitor-2 0 mTOR
IHMT-PI3Kδ-372 0
Parsaclisib (INCB050465) 0
Zandelisib 0
P110δ-IN-1 0
Inavolisib (GDC-0077) 4
SRX3207 0 Syk,BRD42,BRD41
GNE-477 1 mTOR
Selective PI3Kδ Inhibitor 1 (compound 7n) 2
acalisib (GS-9820) 1
leniolisib (CDZ 173) 1 DNA-PK
Bimiralisib (PQR309) 5 mTOR
Seletalisib (UCB-5857) 1
Tenalisib 0
IPI-3063 0
Autophinib 9 Autophagy
Eganelisib (IPI-549) 24
Serabelisib (TAK-117) 3
SF2523 3 DNA-PK,BRD4,mTOR
GDC-0326 2
SAR405 37
umbralisib (TGR-1202) 6
VPS34 inhibitor 1 (Compound 19) 8
Paxalisib (GDC-0084) 3 mTOR
AZD8835 3
Nemiralisib 5
PIK-III 21
VPS34-IN1 30
Voxtalisib (XL765) 14 DNA-PK,mTOR
AMG319 5
AZD8186 18
PF-4989216 1
Pilaralisib (XL147) 14
PI-3065 2
HS-173 20
Quercetin 45 PKC,Src,Sirtuin
Quercetin Dihydrate 9 SIRT1
GSK2636771 18
CAY10505 1
α-Linolenic acid 0
(E)-Akt inhibitor-IV 1
PIK-108 0
SPP-86 0
Resibufogenin 2 cyclin D1,Bax/Bcl-2,Caspase-8
Cinobufagin 0 caspase-9,Bcl-2,Akt
Trigonelline 1 microtubule,Akt,PLCγ1
Ailanthone 1 Akt,CDK,ATM/ATR
MTX-211 2 EGFR
Oroxin B 3 PTEN,Akt,COX-2
Deguelin 4 Akt
Samotolisib (LY3023414) 11 mTOR kinase,DNA-PK
GSK2292767 0
GNE-317 2
点击展开更多
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

生物活性

产品描述 Gambogenic Acid, identified from Gamboge, is an inhibitor of the FGFR signaling pathway in erlotinib-resistant non-small-cell lung cancer (NSCLC) and exhibits anti-tumor effects. Gambogenic acid acts is also an effective inhibitor of EZH2 that specifically and covalently binds to Cys668 within the EZH2-SET domain, and triggers EZH2 ubiquitination.
靶点
FGFR [1] EZH2 [2]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06199531 Recruiting
NGLY1 Deficiency
Grace Science LLC
February 13 2024 Phase 1|Phase 2
NCT05179174 Unknown status
Uveal Melanoma
University of Catania
April 20 2021 --
NCT03838913 Unknown status
Bile Duct Neoplasms|Intraductal Papillary Mucinous Neoplasm
Fujian Provincial Hospital|Fujian Medical University Union Hospital|First Affiliated Hospital of Fujian Medical University
February 15 2019 --
NCT03671525 Completed
Schizophrenia|Schizo Affective Disorder
Johns Hopkins University
October 5 2018 Early Phase 1
NCT02849145 Completed
Uveal Melanoma
Institut Curie
September 2014 Not Applicable

化学信息&溶解度

分子量 630.77 分子式

C38H46O8

CAS号 173932-75-7 SDF --
储存条件(自收到货起) 3年 -20°C 粉状

体外溶解度
批次:

DMSO : 100 mg/mL ( (158.53 mM) ;DMSO吸湿会降低化合物溶解度,请使用新开封DMSO)

摩尔浓度计算器

实验计算

摩尔浓度计算器

质量 浓度 体积 分子量

动物体内配方计算器(澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)

mg/kg g μL

第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系Selleck为您提供正确的澄清溶液配方)

% DMSO % % Tween 80 % ddH2O
%DMSO %

计算结果:

工作液浓度: mg/ml;

DMSO母液配制方法: mg 药物溶于μL DMSO溶液(母液浓度mg/mL,:如该浓度超过该批次药物DMSO溶解度,请先联系Selleck);

体内配方配制方法:μL DMSO母液,加入μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入μL ddH2O,混匀澄清。

体内配方配制方法:μL DMSO母液,加入μL Corn oil,混匀澄清。

注意:1. 首先保证母液是澄清的;
2.一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。

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