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GDC-0084

CAS No.
1382979-44-3
Chemical Name:
GDC-0084
Synonyms
RG7666;CS-2290;RG-7666;GDC-0084;RG 7666);Paxalisib;GDC-0084(RG7666);GDC-0084 (GDC0084;GDC-0084 (Paxalisib;Paxalisib (GDC-0084)
CBNumber:
CB93123145
Molecular Formula:
C18H22N8O2
Molecular Weight:
382.42
MDL Number:
MFCD30187522
MOL File:
1382979-44-3.mol
Last updated:2023-05-21 10:59:17

GDC-0084 Properties

Density 1.60±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility insoluble in H2O; insoluble in EtOH; ≥2.83 mg/mL in DMSO with ultrasonic
pka 2.62±0.40(Predicted)
FDA UNII P5DKZ70636
NCI Drug Dictionary paxalisib

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

GDC-0084 price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth Carbosynth FD145121 GDC 0084 1382979-44-3 1mg $60 2021-12-16 Buy
Biosynth Carbosynth FD145121 GDC 0084 1382979-44-3 2mg $94 2021-12-16 Buy
ApexBio Technology B7826 GDC-0084 1382979-44-3 1mg $95 2021-12-16 Buy
AK Scientific 4658DN Gdc-0084 1382979-44-3 1mg $131 2021-12-16 Buy
ApexBio Technology B7826 GDC-0084 1382979-44-3 10mM(in 1mL DMSO) $158 2021-12-16 Buy
Product number Packaging Price Buy
FD145121 1mg $60 Buy
FD145121 2mg $94 Buy
B7826 1mg $95 Buy
4658DN 1mg $131 Buy
B7826 10mM(in 1mL DMSO) $158 Buy

GDC-0084 Chemical Properties,Uses,Production

Uses

GDC-0084 is an inhibitor of phosphoinositide 3-kinase (PI3K) and mTOR (1,2). Inhibitors of PI3K are useful compounds for developing treatments for brain tumors.

Preparation

Stumpf et al. at Genentech Inc. (Roche group) developed an efficient multikilogram process to synthesize the brain penetrant PI3K inhibitor, GDC?\0084, a potential drug candidate for the treatment of several brain cancers. An efficient Suzuki coupling reaction between a chloropyrimidine and an arylboronic ester using a palladium catalyst at low loading was reported. The optimized conditions were demonstrated on 6.75 kg of a chloropyrimidine intermediate, providing 7.49 kg of crude GDC?\0084 (94% yield, 99.4% HPLC purity). Using the commercially available XPhos Pd G2 catalyst, instead of the usual PdCl2(dppf)·CH2Cl2 catalyst, it was possible to reduce the catalyst loading from 2 to 0.5 mol%. A final scavenging/recrystallization combination from Si?\Thiol (a solid?\supported resin) and acetic acid/water provided the crude GDC?\0084 with the required purity and polymorphic form (off?\white solid, 6.41 kg, 83% yield, 99.7% HPLC purity).
1382979-44-3 synthesis
Genentech’s route to GDC?\0084 employing a pivotal Suzuki reaction.

Biological Activity

gdc-0084 is a potent and brain penetrant inhibitor of pi3k and mtor with ki values of 2 nm and 70 nm for pi3kα and mtor, respectively [1].glioblastoma (gbm) is the most common primary brain tumor in adults and aberrant pi3k signaling is associated with more than 80% of cases. the pi3k pathway represents a potential target for the treatment of this disease and the inhibitors would need to freely cross the blood-brain barrier (bbb) [1][2].gdc-0084 is a potent and brain penetrant inhibitor of pi3k and mtor. in vitro kinase assay, gdc-0084 exhibited ki values of 2 nm, 46 nm, 3 nm, 10 nm and 70 nm for pi3kα, pi3kβ, pi3kδ, pi3kγ and mtor, respectively. in five different gbm cell lines, gdc-0084 had antiproliferative activities with ec50 values ranging from 0.3 to 1.1 μm. gdc-0084 has excellent human metabolic stability in microsomal and hepatocyte incubations [1]. in transfected cell lines over-expressing human or mouse p-gp or bcrp, gdc-0084 was a poor substrate of these efflux transporters. in mice brain, gdc-0084 significantly lowered pakt and ps6 levels [2].in rats after a 15 mg/kg dose of gdc-0084, the total brain-to-plasma ratio was 1.9-3.3. in subcutaneous u87 glioblastoma tumor xenograft mice model, gdc-0084 significantly inhibited tumor growth in a dose-dependent way. gdc-0084 also concentration-dependently inhibited pakt [1].[1]. heffron tp1, ndubaku co1, salphati l1, et al. discovery of clinical development candidate gdc-0084, a brain penetrant inhibitor of pi3k and mtor. acs med chem lett. 2016 feb 16;7(4):351-6.[2]. salphati l, alicke b, heffron tp, et al. brain distribution and efficacy of the brain penetrant pi3k inhibitor gdc-0084 in orthotopic mouse models of human glioblastoma. drug metab dispos. 2016 dec;44(12):1881-1889. epub 2016 sep 16.

GDC-0084 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 93)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
Nanjing Doge Biomedical Technology Co., Ltd
+86-25-58227606 +86-15305155328 sales@dogechemical.com China 4128 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054 trendseenbio@gmail.com China 11681 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8474 58

View Lastest Price from GDC-0084 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
5-[6,6-Dimethyl-4-(4-morpholinyl)-8,9-dihydro-6H-[1,4]oxazino[4,3-e]purin-2-yl]-2-pyrimidinamine pictures 2019-12-23 5-[6,6-Dimethyl-4-(4-morpholinyl)-8,9-dihydro-6H-[1,4]oxazino[4,3-e]purin-2-yl]-2-pyrimidinamine
1382979-44-3
US $1.00 / KG 1KG Min98% HPLC g/kg/ton Career Henan Chemical Co

GDC-0084 Spectrum

GDC-0084 5-[8,9-Dihydro-6,6-dimethyl-4-(4-morpholinyl)-6H-[1,4]oxazino[4,3-e]purin-2-yl]-2-pyrimidinamine 5-(6,6-dimethyl-4-morpholino-8,9-dihydro-6H-[1,4]oxazino[4,3-e]purin-2-yl)pyrimidin-2-amine 2-Pyrimidinamine, 5-[8,9-dihydro-6,6-dimethyl-4-(4-morpholinyl)-6H-[1,4]oxazino[4,3-e]purin-2-yl]- 5-[6,6-Dimethyl-4-(4-morpholinyl)-8,9-dihydro-6H-[1,4]oxazino[4,3-e]purin-2-yl]-2-pyrimidinamine GDC-0084(RG7666) CS-2290 GDC-0084 (GDC0084 RG 7666) RG7666 RG-7666 RG7666; RG-7666; RG 7666; GDC-0084; GDC0084; GDC 0084 GDC-0084;GDC 0084;RG7666;RG-7666;RG 7666 Paxalisib Paxalisib (GDC-0084) GDC-0084 (Paxalisib Paxalisib, GDC-0084, RG7666 1382979-44-3