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Your request to link to MMDB for Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
| MMDB Description | |
|---|---|
| 48826 | Structure Determinants of Phosphoinositide 3-kinase Inhibition by Wortmannin, Ly294002, Quercetin, Myricetin and Staurosporine |
| 48827 | Structure Determinants of Phosphoinositide 3-kinase Inhibition by Wortmannin, Ly294002, Quercetin, Myricetin and Staurosporine |
| 48834 | Structure Determinants of Phosphoinositide 3-kinase Inhibition by Wortmannin, Ly294002, Quercetin, Myricetin and Staurosporine |
| 48835 | Structural Insights Into Phoshoinositide 3-kinase Enzymatic Mechanism and Signalling |
| 48836 | Structure Determinants of Phosphoinositide 3-kinase Inhibition by Wortmannin, Ly294002, Quercetin, Myricetin and Staurosporine |
| 48837 | Structure Determinants of Phosphoinositide 3-kinase Inhibition by Wortmannin, Ly294002, Quercetin, Myricetin and Staurosporine |
| 14576 | Structure Determinants of Phosphoinositide 3-kinase Inhibition by Wortmannin, Ly294002, Quercetin, Myricetin and Staurosporine |
| 49446 | RAS G12v-pi 3-kinase Gamma Complex |
| 35167 | Crystal Structure of Human Pi3kgamma Complexed With As604850 |
| 35169 | Crystal Structure of Human Pi3kgamma Complexed With As605240 |
| 39116 | a Pharmacological MAP of the Pi3-k Family Defines a Role for P110 Alpha in Signaling: the Structure of Complex of Phosphoinositide 3-kinase Gamma With Inhibitor Pik-39 |
| 39117 | a Pharmacological MAP of the Pi3-k Family Defines a Role for P110alpha in Signaling: the Structure of Complex of Phosphoinositide 3-kinase Gamma With Inhibitor Pik-90 |
| 39118 | a Pharmacological MAP of the Pi3-k Family Defines a Role for P110alpha in Signaling: the Structure of Complex of Phosphoinositide 3-kinase Gamma With Inhibitor Pik-93 |
| 67288 | Complex of Human Phosphoinositide 3-kinase Catalytic Subunit Gamma (P110 Gamma) With Pik-284 |
| 89814 | Crystal Structure of Human Pi3k-gamma in Complex With Ch5132799 |
| 89815 | Crystal Structure of Human Pi3k-gamma in Complex With Ch5108134 |
| 89816 | Crystal Structure of Human Pi3k-gamma in Complex With Ch5039699 |
| 64706 | Crystal Structure of Pi3k P110gamma Catalytical Domain in Complex With Organoruthenium Inhibitor DW2 |
| 64590 | Crystal Structure of Pi3k P110gamma Catalytical Domain in Complex With Organoruthenium Inhibitor E5e2 |
| 65020 | Structure of Pi3k Gamma in Complex With Gdc0941 |
| 66340 | Achieving Multi-isoform Pi3k Inhibition in a Series of Substituted 3,4-dihydro-2h-benzo[1,4]oxazines |
| 67378 | Complex of Pi3k Gamma With an Inhibitor |
| 76492 | Crystal Structure of a Pyrazolopyrimidine Inhibitor Bound to PI3 Kinase Gamma |
| 82933 | Structure of Pi3k Gamma With a Potent Inhibitor: Gsk2126458 |
| 80174 | Crystal Structures of Pan-pi3-kinase and Dual Pan-pi3-kinasemtor Inhibitors |
| 80175 | Discovery of (Thienopyrimidin-2-yl)aminopyrimidines as Potent, Selective, and Orally Available Pan-pi3-kinase and Dual Pan-pi3- Kinasemtor Inhibitors for the Treatment of Cancer |
| 80176 | Discovery of (Thienopyrimidin-2-yl)aminopyrimidines as Potent, Selective, and Orally Available Pan-pi3-kinase and Dual Pan-pi3- Kinasemtor Inhibitors for the Treatment of Cancer |
| 83054 | Structure of Pi3k Gamma With Inhibitor |
| 81414 | Pi3-kinase-gamma With a Pyrrolopyridine-benzofuran Inhibitor |
| 82651 | PI3 Kinase Gamma With a Benzofuranone Inhibitor |
| 82505 | Discovery of the Highly Potent Pi3kmtor Dual Inhibitor Pf-0 Through Structure Based Drug Design |
| 82506 | Discovery of the Highly Potent Pi3kmtor Dual Inhibitor Pf-0 Through Structure Based Drug Design |
| 87615 | Structure-based Optimization of Pyrazolo -Pyrimidine and -Pyridine Inhibitors of Pi3-kinase |
| 87616 | Structure-based Optimization of Pyrazolo -Pyrimidine and -Pyridine Inhibitors of Pi3-kinase |
| 85074 | 4-methylpteridineones as Orally Active and Selective Pi3kmtor Dual Inhibitors |
| 88565 | Quinazolines With Intra-molecular Hydrogen Bonding Scaffold (Imhbs) as Pi3kmtor Dual Inhibitors |
| 88566 | Quinazolines With Intra-molecular Hydrogen Bonding Scaffold (Imhbs) as Pi3kmtor Dual Inhibitors |
| 88567 | Quinazolines With Intra-molecular Hydrogen Bonding Scaffold (Imhbs) as Pi3kmtor Dual Inhibitors |
| 89554 | Crystal Structure of Pi3k-gamma in Complex With Triazine-benzimidazole 1 |
| 89555 | Crystal Structure of Pi3k-gamma in Complex With Triazine-benzimidazole 32 |
| 89560 | Crystal Structure of Pi3k-gamma in Complex With Benzothiazole 1 |
| 89561 | Crystal Structure of Pi3k-gamma in Complex With Benzothiazole 82 |
| 91273 | Crystal Structure of Pi3k-gamma in Complex With a Quinoline Inhibitor |