Model NO.: CAS: 912444-00-9
Trademark: Quanao
Transport Package: Safe and Discreet Packing Ways
Specification: 100mg/bag
Origin: Guangzhou China
HS Code: 2501001900
Model NO.: CAS: 912444-00-9
Trademark: Quanao
Transport Package: Safe and Discreet Packing Ways
Specification: 100mg/bag
Origin: Guangzhou China
HS Code: 2501001900
Veliparib CAS :Â 912444-00-9MF:Â Â Â Â C13H16N4O.2ClH
MW:Â Â Â Â 317.218
Chemical Name :(R)-2-(2-methylpyrrolidin-2-yl)-1H-benzo[d]imidazole-4-carboxamide
Veliparib (ABT-888) is a potential anti-cancer drug acting as a PARP inhibitor. It kills cancer cells by blocking a protein called PARP, thereby preventing the repair of DNA or genetic damage in cancer cells and possibly making them more susceptible to anticancer treatments. Veliparib may make whole brain radiation treatment work more effectively against brain metastases from NSCLC.
Biological activity
Veliparib (ABT-888) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM and 2.9 nM, respectively, and inhibits SIRT2. Phase 3.
In vitro study
ABT-888 effectively inhibited PARP, and the Ki values were 5.2 and 2.9 nM for PARP-1 and PARP-2, respectively. ABT-888 reduced the survival rate of cloned genes in lung cancer H460 cells and inhibited DNA repair. ABT-888 inhibited C41 cells with an EC50 of 2Â nM. ABT-888 and radiotracer to reduce tumor angiogenesis.
In vivo studies
ABT-888 delayed tumor growth in NCI-H460 xenograft tumor model. ABT-888 inhibits PARP in the B16F10 and 9L xenograft models, thereby enhancing the anticancer activity of temozolomide. The combination of ABT-888 and Other cytotoxic agents showed potent anti-cancer effects in the MX-1 xenograft model. In the A375 and Colo829 xenograft models, tumor size was increased by 3Â and 12.5 mg ABT-888 per kilogram, respectively, and more than 95% of the PAR in the tumor was inhibited.
feature
ABT-888 enhances the effectiveness of common cancer therapies, such as radiotherapy and alkylating agents.
Product name
Veliparib/ABT 888
Synonyms
2-[(2R)-2-Methyl-2-pyrrolidinyl]-1H-benzimidazole-7-carboxamide
CAS No.
912444-00-9
Molecular formula
C13H16N4O
Molecular weight
244.29
Appearance
White powder
Boiling point
579.023°C at 760 mmHg
Assay   Â
99%
Packing
100mg ;Â 1g;10g;25g;50g;100g;200g;500g;1Kg
Application
Pharmaceutical Intermediates
Here Guangzhou Quanao chemical Co. Ltd is one of the worlds high-tech enterprise with completely independent intellectual property rights specialized in flavor, steroid powders , semi-finished steroid liquids , Sarm powders  , fragrance, chemical raw material, food additives, cinnamon series, plant extracts, pharmaceutical Products and high-quality powders for sale over several years. We offer you "safety, efficiency, Security" service. Get the service and products Here, we will offer you special discount. Any questions will be welcomed.
Relate Inhibitors products contact Bruce
ABT-888Â Â Â Â
AZD2281Â Â Â Â
GSK2126458Â Â Â Â
BMS777607Â Â Â Â
BMS5121458Â Â Â Â
VX950Â Â Â Â
Telatinib (BAY 57-9352)Â Â Â Â
gsk1904529AÂ Â Â Â
LY2157299Â Â Â Â
DMXAA(AS1404,ASA404)Â Â Â Â
Brivanib(bms-540215)Â Â Â Â
Brivanib alaninate(BMS-582664)Â Â Â Â
vx-702Â Â Â Â
abt-869Â Â Â Â
NPS-2143Â Â Â Â
AG014699Â Â Â Â
AZD6244Â Â Â Â
GSK1070916Â Â Â Â
GSK1120212Â Â Â Â
A-674563Â Â Â Â
MLN8237Â Â Â Â
AS605240Â Â Â Â
YO01027Â Â Â Â
PKI587Â Â Â Â
LY2886721Â Â Â Â
PF299804Â Â Â Â
GSK690693Â Â Â Â
PF-04691502Â Â Â Â
SRT1720Â Â Â Â
PP242Â Â Â Â
KW-2478Â Â Â Â
YM201636Â Â Â Â
ms-275Â Â Â Â
PI-103Â Â Â Â
PKI-402Â Â Â Â
GDC0980Â Â Â Â
GSK1292263Â Â Â Â
PHA665752Â Â Â Â
LY573636Â Â Â Â
AZD8055Â Â Â Â
KU0063794Â Â Â Â
MDV3100Â Â Â Â
AST-1306Â Â Â Â
Apixaban   Â
MGCD0103Â Â Â Â
XL880Â Â Â Â
MGCD265Â Â Â Â
sns032Â Â Â Â
ABT-263Â Â Â Â
ABT-737Â Â Â Â
NVP-BGJ398Â Â Â Â
BAY73-4506Â Â Â Â
Roflumilast,Daxas   Â
Fasudil hydrochloride   Â
Pelitinib(EKB-569)Â Â Â Â
Neratinib(HKI-272)Â Â Â Â
Imatinib   Â
Erlotinib HCLÂ Â Â Â
Afatinib(BIBW2992)Â Â Â Â
PCI-32765Â Â Â Â
AP24534(Ponatinib)Â Â Â Â
AT101Â Â Â Â
AZD5438Â Â Â Â
CX-4945Â Â Â Â
LY2109761Â Â Â Â
RAF265Â Â Â Â
LY294002Â Â Â Â
KU55933Â Â Â Â
XL184Â Â Â Â
Linagliptin   Â
FUB359Â Â Â Â
Canetinib   Â
Laquinimod   Â
Mastinib   Â
Torcetrapib   Â
Tasosartan   Â
A-803467Â Â Â Â
JTC801Â Â Â Â
Pyroxamide   Â
CP466722Â Â Â Â
PF-562771Â Â Â Â
TAK285Â Â Â Â
ARN-509Â Â Â Â
OC000459Â Â Â Â
HQL-79Â Â Â Â
JTT705Â Â Â Â
MK-5108(VX689)Â Â Â Â
LY2811376Â Â Â Â
ctep   Â
PF-02341066Â Â Â Â
TAK438Â Â Â Â
IOX2Â Â Â Â
GNF-2Â Â Â Â
THIACETAZONEÂ Â Â Â
PD0325901Â Â Â Â
R406Â Â Â Â
AT-406Â Â Â Â
R547Â Â Â Â
CB-7598Â Â Â Â
CB7630Â Â Â Â
R788Â Â Â Â
VU0364439Â Â Â Â
TDZD-8Â Â Â Â
VU 0361737Â Â Â Â
TCS PIM-1 4a   Â
YS-49Â Â Â Â
YM-90K hydrochloride   Â
PAI-039Â Â Â Â Â
Dapivirine   Â
WZ 811Â Â Â Â Â
TTP 22Â Â Â Â Â
AG-490Â Â Â Â
D-6413Â Â Â Â
DY131Â Â Â Â
GW 788388Â Â Â Â
Merck-5 ,JAK INHIBITOR IÂ Â Â Â Â
JAK2 Inhibitor VÂ Â Z3Â Â Â Â
KU14RÂ Â Â Â Â
LDN-211904Â Â Â Â
MK 886Â Â Â Â
TAC-101Â Â Â Â Â
3-MAÂ Â Â Â
PHT427Â Â Â Â
GW7647Â Â Â Â
LY364947Â Â Â Â
SB203580Â Â Â Â
ZM323881Â Â Â Â
ZM306416Â Â Â Â
PF8380Â Â Â Â
RITA (NSC 652287)Â Â Â Â
ACY-1215Â Â Â Â
ASP3026Â Â Â Â
sch900776Â Â Â Â
CP-945598Â Â Â Â
OSI-027Â Â Â Â
SB431542Â Â Â Â
LY2623091Â Â Â Â
Tenovin-1Â Â Â Â Â
Apoptosis Activator 2Â Â Â Â Â
HA14-1Â Â Â Â
SMI-4a   Â
TWS119Â Â Â Â
VU 0364439Â Â Â Â
LY315920Â Â Â Â
Anamorelin   Â
AZD2014Â Â Â Â
LY2940680Â Â Â Â
LY500307Â Â Â Â
LY2608204Â Â Â Â
TAK700Â Â Â Â
Linagliptin(BI-1356)Â Â Â Â
NVP-BHG712Â Â Â Â
Amrubicin    Â
WAY362450Â Â Â Â
AZD8931Â Â Â Â
 Veliparib CAS : 912444-00-9
MF:Â Â Â Â C13H16N4O.2ClH
MW:Â Â Â Â 317.218
Chemical Name :(R)-2-(2-methylpyrrolidin-2-yl)-1H-benzo[d]imidazole-4-carboxamide
Veliparib (ABT-888) is a potential anti-cancer drug acting as a PARP inhibitor. It kills cancer cells by blocking a protein called PARP, thereby preventing the repair of DNA or genetic damage in cancer cells and possibly making them more susceptible to anticancer treatments. Veliparib may make whole brain radiation treatment work more effectively against brain metastases from NSCLC.
Biological activity
Veliparib (ABT-888) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM and 2.9 nM, respectively, and inhibits SIRT2. Phase 3.
In vitro study
ABT-888 effectively inhibited PARP, and the Ki values were 5.2 and 2.9 nM for PARP-1 and PARP-2, respectively. ABT-888 reduced the survival rate of cloned genes in lung cancer H460 cells and inhibited DNA repair. ABT-888 inhibited C41 cells with an EC50 of 2Â nM. ABT-888 and radiotracer to reduce tumor angiogenesis.
In vivo studies
ABT-888 delayed tumor growth in NCI-H460 xenograft tumor model. ABT-888 inhibits PARP in the B16F10 and 9L xenograft models, thereby enhancing the anticancer activity of temozolomide. The combination of ABT-888 and other cytotoxic agents showed potent anti-cancer effects in the MX-1 xenograft model. In the A375 and Colo829 xenograft models, tumor size was increased by 3Â and 12.5 mg ABT-888 per kilogram, respectively, and more than 95% of the PAR in the tumor was inhibited.
feature
ABT-888 enhances the effectiveness of common cancer therapies, such as radiotherapy and alkylating agents.
Product name
Veliparib/ABT 888
Synonyms
2-[(2R)-2-Methyl-2-pyrrolidinyl]-1H-benzimidazole-7-carboxamide
CAS No.
912444-00-9
Molecular formula
C13H16N4O
Molecular weight
244.29
Appearance
White powder
Boiling point
579.023°C at 760 mmHg
Assay   Â
99%
Packing
100mg ;Â 1g;10g;25g;50g;100g;200g;500g;1Kg
Application
Pharmaceutical Intermediates
Here Guangzhou Quanao chemical Co. Ltd is one of the worlds high-tech enterprise with completely independent intellectual property rights specialized in flavor, steroid powders , semi-finished steroid liquids , Sarm powders  , fragrance, chemical raw material, food additives, cinnamon series, plant extracts, pharmaceutical Products and high-quality powders for sale over several years. We offer you "safety, efficiency, Security" service. Get the service and products Here, we will offer you special discount. Any questions will be welcomed.
Relate Inhibitors products contact Bruce
ABT-888Â Â Â Â
AZD2281Â Â Â Â
GSK2126458Â Â Â Â
BMS777607Â Â Â Â
BMS5121458Â Â Â Â
VX950Â Â Â Â
Telatinib (BAY 57-9352)Â Â Â Â
gsk1904529AÂ Â Â Â
LY2157299Â Â Â Â
DMXAA(AS1404,ASA404)Â Â Â Â
Brivanib(bms-540215)Â Â Â Â
Brivanib alaninate(BMS-582664)Â Â Â Â
vx-702Â Â Â Â
abt-869Â Â Â Â
NPS-2143Â Â Â Â
AG014699Â Â Â Â
AZD6244Â Â Â Â
GSK1070916Â Â Â Â
GSK1120212Â Â Â Â
A-674563Â Â Â Â
MLN8237Â Â Â Â
AS605240Â Â Â Â
YO01027Â Â Â Â
PKI587Â Â Â Â
LY2886721Â Â Â Â
PF299804Â Â Â Â
GSK690693Â Â Â Â
PF-04691502Â Â Â Â
SRT1720Â Â Â Â
PP242Â Â Â Â
KW-2478Â Â Â Â
YM201636Â Â Â Â
ms-275Â Â Â Â
PI-103Â Â Â Â
PKI-402Â Â Â Â
GDC0980Â Â Â Â
GSK1292263Â Â Â Â
PHA665752Â Â Â Â
LY573636Â Â Â Â
AZD8055Â Â Â Â
KU0063794Â Â Â Â
MDV3100Â Â Â Â
AST-1306Â Â Â Â
Apixaban   Â
MGCD0103Â Â Â Â
XL880Â Â Â Â
MGCD265Â Â Â Â
sns032Â Â Â Â
ABT-263Â Â Â Â
ABT-737Â Â Â Â
NVP-BGJ398Â Â Â Â
BAY73-4506Â Â Â Â
Roflumilast,Daxas   Â
Fasudil hydrochloride   Â
Pelitinib(EKB-569)Â Â Â Â
Neratinib(HKI-272)Â Â Â Â
Imatinib   Â
Erlotinib HCLÂ Â Â Â
Afatinib(BIBW2992)Â Â Â Â
PCI-32765Â Â Â Â
AP24534(Ponatinib)Â Â Â Â
AT101Â Â Â Â
AZD5438Â Â Â Â
CX-4945Â Â Â Â
LY2109761Â Â Â Â
RAF265Â Â Â Â
LY294002Â Â Â Â
KU55933Â Â Â Â
XL184Â Â Â Â
Linagliptin   Â
FUB359Â Â Â Â
Canetinib   Â
Laquinimod   Â
Mastinib   Â
Torcetrapib   Â
Tasosartan   Â
A-803467Â Â Â Â
JTC801Â Â Â Â
Pyroxamide   Â
CP466722Â Â Â Â
PF-562771Â Â Â Â
TAK285Â Â Â Â
ARN-509Â Â Â Â
OC000459Â Â Â Â
HQL-79Â Â Â Â
JTT705Â Â Â Â
MK-5108(VX689)Â Â Â Â
LY2811376Â Â Â Â
ctep   Â
PF-02341066Â Â Â Â
TAK438Â Â Â Â
IOX2Â Â Â Â
GNF-2Â Â Â Â
THIACETAZONEÂ Â Â Â
PD0325901Â Â Â Â
R406Â Â Â Â
AT-406Â Â Â Â
R547Â Â Â Â
CB-7598Â Â Â Â
CB7630Â Â Â Â
R788Â Â Â Â
VU0364439Â Â Â Â
TDZD-8Â Â Â Â
VU 0361737Â Â Â Â
TCS PIM-1 4a   Â
YS-49Â Â Â Â
YM-90K hydrochloride   Â
PAI-039Â Â Â Â Â
Dapivirine   Â
WZ 811Â Â Â Â Â
TTP 22Â Â Â Â Â
AG-490Â Â Â Â
D-6413Â Â Â Â
DY131Â Â Â Â
GW 788388Â Â Â Â
Merck-5 ,JAK INHIBITOR IÂ Â Â Â Â
JAK2 Inhibitor VÂ Â Z3Â Â Â Â
KU14RÂ Â Â Â Â
LDN-211904Â Â Â Â
MK 886Â Â Â Â
TAC-101Â Â Â Â Â
3-MAÂ Â Â Â
PHT427Â Â Â Â
GW7647Â Â Â Â
LY364947Â Â Â Â
SB203580Â Â Â Â
ZM323881Â Â Â Â
ZM306416Â Â Â Â
PF8380Â Â Â Â
RITA (NSC 652287)Â Â Â Â
ACY-1215Â Â Â Â
ASP3026Â Â Â Â
sch900776Â Â Â Â
CP-945598Â Â Â Â
OSI-027Â Â Â Â
SB431542Â Â Â Â
LY2623091Â Â Â Â
Tenovin-1Â Â Â Â Â
Apoptosis Activator 2Â Â Â Â Â
HA14-1Â Â Â Â
SMI-4a   Â
TWS119Â Â Â Â
VU 0364439Â Â Â Â
LY315920Â Â Â Â
Anamorelin   Â
AZD2014Â Â Â Â
LY2940680Â Â Â Â
LY500307Â Â Â Â
LY2608204Â Â Â Â
TAK700Â Â Â Â
Linagliptin(BI-1356)Â Â Â Â
NVP-BHG712Â Â Â Â
Amrubicin    Â
WAY362450Â Â Â Â
AZD8931Â Â Â Â
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