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NVP-ADW7

NVP-ADW742

CAS: 475488-23-4

Molecular Formula: C28H31N5O

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NVP-ADW7 - Names and Identifiers

Name NVP-ADW742
Synonyms ADW
ADW 742
NVP-ADW7
NVP-ADW742
NVP-ADW742(ADW742)
ADW 742 GSK 552602A
5-(3-(Benzyloxy)phenyl)-7-((1r,3r)-3-(pyrrolidin-1-ylmethyl)-cyclobutyl)-7H-pyrrolo[2,3-d]pyri
5-(3-Benzyloxyphenyl)-7-[trans-3-[(pyrrolidin-1-yl)methyl]cyclobutyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
5-(3-Benzyloxyphenyl)-7-[trans-3-[(pyrrolidin-1-yl)methyl]cyclobutyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine NVP-ADW742 GSK 552602A
CAS 475488-23-4

NVP-ADW7 - Physico-chemical Properties

Molecular FormulaC28H31N5O
Molar Mass453.58
Density1.31
Boling Point677.5±55.0 °C(Predicted)
Solubility DMSO:10 mg/mL heat (22 mM),Water:<1 mg/mL (<1 mM),Ethanol:3 mg/mL (6 mM)
pKa10.00±0.20(Predicted)
Storage Condition-20℃
UseAn IGF-1R inhibitor with IC50 of 0.17 μM
In vitro studyNVP-ADW742 is more than 6 times more selective at IGF-1R than at insulin receptor (InsR), with an IC50 of 2.8 μm, and has the lowest inhibitory activity at c-Kit, HER1, PDGFR, VEGFR-2, or Bcr-Abl p210, IC50>5-10 μm, consistent with significant inhibition of IGF-1-induced phosphorylation of IGF-1R and its downstream target, Akt. NVP-ADW742 significantly inhibited the proliferation of a variety of cells stimulated by serum in a dose-dependent manner, with IC50 of 0.1-0.5 μm in multiple myeloma (MM) cell lines, co-culture with BMSCs could not overcome the anticancer effect on MM. In the presence of serum, NVP-ADW742 also abrogated the tumor cell response to IL-6. In addition, NVP-ADW742 effectively acts on MM cell lines against conventional anti-cancer agents (toxic chemotherapeutic agents, Dexamethasone) or anti-cancer agents for research (Thalidomide, CC-5013, TRAIL/Apo2L, PS-341), it also effectively acts on primary tumor cells in MM patients who are resistant to multiple drugs. NVP-ADW742 acts on tumor cells and bone marrow stromal stem cells, reduces VEGF production, and inhibits IGF-1-induced VEGF secretion in a variety of tumor types, such as thyroid cancer cells and MM cells. The 0.75 μm NVP-ADW742 inhibits IGF-1R and also sensitizes MM cells or prostate cancer cells to other anti-cancer agents such as Doxorubicin, Melphalan, Dexamethasone, TRAIL/Apo2L, or PS-341.
In vivo studyNVP-ADW742 treatment of a mouse model with diffusion MM at a dose of 10 mg/kg twice daily significantly inhibited tumor growth, prolonged life, and enhanced anti-cancer effects.

NVP-ADW7 - Introduction

NVP-ADW742 is a IGF-1R inhibitor with IC50 of 0.17 μM, which is more than 16 times stronger on IGF-1R than on InsR. It has little activity on HER2, PDGFR, VEGFR-2, Bcr-Abl and c-Kit.
Last Update:2022-10-16 17:41:40
NVP-ADW7
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MedChemExpress (MCE)
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CAS: 475488-23-4
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MedChemExpress (MCE)
Spot supply
Product Name: ADW742; GSK 552602A; ADW Visit Supplier Webpage Request for quotation
CAS: 475488-23-4
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: NVP-ADW742 Visit Supplier Webpage Request for quotation
CAS: 475488-23-4
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
WhatsApp: +86-18621343501
Shanghai Macklin Biochemical Co., Ltd
Spot supply
Product Name: NVP-ADW742 Visit Supplier Webpage Request for quotation
CAS: 475488-23-4
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: NVP-ADW742 Visit Supplier Webpage Request for quotation
CAS: 475488-23-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
View History
NVP-ADW7
3-Piperidin-4-ylmethyl-isoquinoline dihydrochloride
(2E)-1-{3-[(2,4-dichlorophenyl)methoxy]phenyl}-3-[(4-ethylphenyl)amino]prop-2-en-1-one
(3,4-Dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl)methanamine hydrochloride
9-octadecenylester,(z)-hexadecanoicaci
cockscomb
924869-27-2
派洛宁Y(IND GRADE)
2-[exo-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl]acetic acid
S-butan-2-yl 3-methylbut-2-enethioate
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