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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H16Cl2F2N4O2.ClH
Molecular Weight 465.709
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of UPROSERTIB HYDROCHLORIDE

SMILES

Cl.CN1N=CC(Cl)=C1C2=C(Cl)OC(=C2)C(=O)N[C@H](CN)CC3=CC=C(F)C(F)=C3

InChI

InChIKey=LAPFKCIDRPWAFU-PPHPATTJSA-N
InChI=1S/C18H16Cl2F2N4O2.ClH/c1-26-16(12(19)8-24-26)11-6-15(28-17(11)20)18(27)25-10(7-23)4-9-2-3-13(21)14(22)5-9;/h2-3,5-6,8,10H,4,7,23H2,1H3,(H,25,27);1H/t10-;/m0./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C18H16Cl2F2N4O2
Molecular Weight 429.248
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Uprosertib is an oral potent Akt inhibitor which acts equally on Akt1, Akt2 and Akt3. The drug is under clinical development in combination with trametinib for the treatment of different cancers, including melanoma, myeloma, breast, endometrial, cervical cancer, etc.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
180.0 nM [IC50]
38.0 nM [IC50]
328.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
409 ng/mL
75 mg 1 times / day steady-state, oral
dose: 75 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
UPROSERTIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
94.6 ng/mL
75 mg single, oral
dose: 75 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
UPROSERTIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
6383 ng × h/mL
75 mg 1 times / day steady-state, oral
dose: 75 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
UPROSERTIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
1262 ng × h/mL
75 mg single, oral
dose: 75 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
UPROSERTIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
63.7 h
75 mg 1 times / day steady-state, oral
dose: 75 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
UPROSERTIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Discovery of novel AKT inhibitors with enhanced anti-tumor effects in combination with the MEK inhibitor.
2014
Patents

Sample Use Guides

Melanoma: patients receive oral uprosertib at a dose 25 mg daily. Cervical Cancer: the dose is 50 mg orally once per day.
Route of Administration: Oral
Human lung fibroblasts were treated with uprosertib in concentration range from 20 nM to 1.28 uM and analyzed for type I collagen expression. At concentration of 320 nM or higher the drug reduced intracellular level of collagen alpha2(I) polypeptide, while it reduced intracellular alpha olypeptide at concentrations > 640 nM.
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:56:23 GMT 2025
Edited
by admin
on Mon Mar 31 22:56:23 GMT 2025
Record UNII
50IE5H22B2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
UPROSERTIB HYDROCHLORIDE
Common Name English
2-FURANCARBOXAMIDE, N-((1S)-2-AMINO-1-((3,4-DIFLUOROPHENYL)METHYL)ETHYL)-5-CHLORO-4-(4-CHLORO-1-METHYL-1H-PYRAZOL-5-YL)-, HYDROCHLORIDE (1:1)
Preferred Name English
Code System Code Type Description
DRUG BANK
DBSALT002113
Created by admin on Mon Mar 31 22:56:23 GMT 2025 , Edited by admin on Mon Mar 31 22:56:23 GMT 2025
PRIMARY
FDA UNII
50IE5H22B2
Created by admin on Mon Mar 31 22:56:23 GMT 2025 , Edited by admin on Mon Mar 31 22:56:23 GMT 2025
PRIMARY
PUBCHEM
73330428
Created by admin on Mon Mar 31 22:56:23 GMT 2025 , Edited by admin on Mon Mar 31 22:56:23 GMT 2025
PRIMARY
SMS_ID
300000013042
Created by admin on Mon Mar 31 22:56:23 GMT 2025 , Edited by admin on Mon Mar 31 22:56:23 GMT 2025
PRIMARY
CAS
1047635-80-2
Created by admin on Mon Mar 31 22:56:23 GMT 2025 , Edited by admin on Mon Mar 31 22:56:23 GMT 2025
PRIMARY
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