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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H30F2N6O3
Molecular Weight 560.5944
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0
Stereo Comments AXIAL, R

SHOW SMILES / InChI
Structure of SOTORASIB

SMILES

CC(C)C1=C(N2C(=O)N=C(N3CCN(C[C@@H]3C)C(=O)C=C)C4=CC(F)=C(N=C24)C5=C(O)C=CC=C5F)C(C)=CC=N1

InChI

InChIKey=NXQKSXLFSAEQCZ-SFHVURJKSA-N
InChI=1S/C30H30F2N6O3/c1-6-23(40)36-12-13-37(18(5)15-36)28-19-14-21(32)26(24-20(31)8-7-9-22(24)39)34-29(19)38(30(41)35-28)27-17(4)10-11-33-25(27)16(2)3/h6-11,14,16,18,39H,1,12-13,15H2,2-5H3/t18-/m0/s1

HIDE SMILES / InChI

Description

Sotorasib (LUMAKRAS™) is a RAS GTPase family inhibitor being developed by Amgen for the treatment of solid tumours with KRAS mutations, including non-small cell lung cancer (NSCLC) and colorectal cancer. Sotorasib is an inhibitor of KRASG12C, a tumor-restricted, mutant-oncogenic form of the RAS GTPase, KRAS. Sotorasib forms an irreversible, covalent bond with the unique cysteine of KRASG12C, locking the protein in an inactive state that prevents downstream signaling without affecting wild-type KRAS. Sotorasib blocked KRAS signaling, inhibited cell growth, and promoted apoptosis only in KRAS G12C tumor cell lines. Sotorasib inhibited KRASG12C in vitro and in vivo with minimal detectable off-target activity. In May 2021, sotorasib was granted accelerated approval by the US FDA for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic NSCLC, as determined by an FDA-approved test, who have received at least one prior systemic therapy.

CNS Activity

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
30.0 nM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
LUMAKRAS

Cmax

ValueDoseCo-administeredAnalytePopulation
6.44 μg/mL
180 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
6.31 μg/mL
360 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
5.45 μg/mL
720 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
5.39 μg/mL
960 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
6690 ng/mL
960 mg single, oral
SOTORASIB plasma
Homo sapiens
7880 ng/mL
960 mg single, oral
SOTORASIB plasma
Homo sapiens
8320 ng/mL
960 mg 1 times / day multiple, oral
SOTORASIB plasma
Homo sapiens
7180 ng/mL
960 mg 1 times / day multiple, oral
SOTORASIB plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
31.7 μg × h/mL
180 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
38.9 μg × h/mL
360 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
42.1 μg × h/mL
720 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
32.4 μg × h/mL
960 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
28700 ng × h/mL
960 mg single, oral
SOTORASIB plasma
Homo sapiens
31500 ng × h/mL
960 mg single, oral
SOTORASIB plasma
Homo sapiens
81500 ng × h/mL
960 mg 1 times / day multiple, oral
SOTORASIB plasma
Homo sapiens
43900 ng × h/mL
960 mg 1 times / day multiple, oral
SOTORASIB plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
5.13 h
180 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
5.53 h
360 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
4.75 h
720 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens
5.07 h
960 mg 1 times / day steady-state, oral
SOTORASIB plasma
Homo sapiens

Funbound

ValueDoseCo-administeredAnalytePopulation
11.2%
SOTORASIB plasma
Homo sapiens

Doses

AEs

Drug as perpetrator​

Drug as victim

Tox targets

PubMed

Sample Use Guides

In Vivo Use Guide
https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/214665s000lbl.pdf
Route of Administration: Oral
In Vitro Use Guide
Sotorasib inhibited the SOS1- catalyzed nucleotide exchange of KRASG12C (IC50 = 92.6 nM or ~51.9 ng/mL) but not wild-type (WT) KRAS (IC50 >250 uM).