| KRAS G12C warhead (acrylamide pharmacophore)Abstract pharmacophorekras-g12c-warheadPage | Scaffold | C=CC(=O)Nc1ccc(F)cc1 | — | — | KRAS G12C · covalent · core · warhead · Hinge-binding acrylamide — common origin for covalent G12C series. |
| Adagrasib (Krazati)Verified drugadagrasibPage | Drug | CC(C)C1=NC(=C(N1)C2=CC=CC=C2)C3=CC4=C(C=C3… | KRAS G12C warhead (acrylamide pharmacophore) | 13%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | approved · KRAS G12C · Krazati · KRAS G12C inhibitor with long half-life (Krazati). · CHEMBL4594350 · CID 138565341 |
| DaraxonrasibKnown compounddaraxonrasib-kras-nodePage | Drug | C[C@H]1CN(C(=O)C2=C(NC3=CC=CC(F)=C3)N=C(N2… | KRAS G12C warhead (acrylamide pharmacophore) | 16%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | KRAS G12C · clinical · Clinical-stage candidate. Daraxonrasib in this family map. |
| Divarasib (GDC-6036)Known compounddivarasibPage | Drug | C[C@H]1CN(C(=O)C2=C(NC3=CC=CC(F)=C3)N=C(N2… | KRAS G12C warhead (acrylamide pharmacophore) | 16%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | KRAS G12C · clinical · Clinical-stage candidate. Divarasib (GDC-6036) in this family map. |
| Garsorasib (D-1553)Known compoundgarsorasibPage | Drug | C[C@H]1CN(C(=O)c2ccc(F)cc2NC(=O)C3=C(Nc4cc… | KRAS G12C warhead (acrylamide pharmacophore) | 20%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | KRAS G12C · clinical · Clinical KRAS G12C inhibitor (D-1553) — distinct chemotype from sotorasib. |
| Olomorasib (LY3537982)Known compoundolomorasibPage | Drug | C[C@H]1CN(C(=O)C2=C(NC3=CC=CC(Cl)=C3)N=C(N… | KRAS G12C warhead (acrylamide pharmacophore) | 12%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | clinical · KRAS G12C · Clinical-stage candidate. Olomorasib (LY3537982) in this family map. |
| Sotorasib (Lumakras)Verified drugsotorasibPage | Drug | C[C@H]1CN(C(=O)C2=C(NC3=CC=CC(F)=C3)N=C(N2… | KRAS G12C warhead (acrylamide pharmacophore) | 16%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | approved · KRAS G12C · Lumakras · First approved covalent KRAS G12C inhibitor (Lumakras). · CHEMBL4297837 · CID 118023034 |
| KRAS chloro-bridge analogExploratory analog (rule-generated)kras-sar-cl-bridgePage | Derivative | C=CC(=O)Nc1ccc(F)cc1NCc1ccc(Cl)cc1 | KRAS SAR analog B (from analog A) | 42%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | SAR · SAR exploration node. Derived analog of parent node in KRAS G12C inhibitor chemical landsc… |
| KRAS piperazine SAR analogExploratory analog (rule-generated)kras-sar-piperazinePage | Derivative | C=CC(=O)Nc1ccc(F)cc1N1CCNCC1 | KRAS SAR analog A (F-aryl walk) | 43%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | SAR · SAR exploration node. Derived analog of parent node in KRAS G12C inhibitor chemical landsc… |
| KRAS PROTAC hybrid 1Exploratory analogkras-protac-1Page | Derivative | C[C@H]1CN(C(=O)C2=C(NC3=CC=CC(F)=C3)N=C(N2… | Sotorasib (Lumakras) | 12%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | PROTAC · degrader · SAR / analog node exploring potency, selectivity, or ADME. |
| KRAS SAR analog A (F-aryl walk)Exploratory analog (rule-generated)kras-sar-analog-aPage | Derivative | C=CC(=O)Nc1ccc(F)cc1NC2=CC=CC=C2 | KRAS G12C warhead (acrylamide pharmacophore) | 51%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | SAR · derivative · SAR exploration node. Derived analog of parent node in KRAS G12C inhibitor chemical landsc… |
| KRAS SAR analog B (from analog A)Exploratory analog (rule-generated)kras-sar-analog-bPage | Derivative | C=CC(=O)Nc1ccc(F)cc1NC2=CC=C(Cl)C=C2 | KRAS SAR analog A (F-aryl walk) | 53%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | SAR · ADME · SAR exploration node. Derived analog of parent node in KRAS G12C inhibitor chemical landsc… |
| KRAS-targeted payload analog 1Payloadkras-adc-payload-1Page | Payload | C=CC(=O)Nc1ccc(F)cc1NC(=O)CCN | KRAS G12C warhead (acrylamide pharmacophore) | 45%iStructural similarity calculated using Morgan fingerprint (RDKit circular fingerprint, radius 2, 2048 bits) with Tanimoto similarity. Structural similarity does not predict biological equivalence, potency, safety, or clinical efficacy. | payload · ADC-design · Payload warhead chemistry. Released warhead after lysosomal cleavage. |