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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H18ClF5N6O
Molecular Weight 464.82
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CEVIPABULIN

SMILES

CNCCCOC1=CC(F)=C(C(F)=C1)C2=C(N[C@@H](C)C(F)(F)F)N3N=CN=C3N=C2Cl

InChI

InChIKey=ZUZPCOQWSYNWLU-VIFPVBQESA-N
InChI=1S/C18H18ClF5N6O/c1-9(18(22,23)24)28-16-14(15(19)29-17-26-8-27-30(16)17)13-11(20)6-10(7-12(13)21)31-5-3-4-25-2/h6-9,25,28H,3-5H2,1-2H3/t9-/m0/s1

HIDE SMILES / InChI
Cevipabulin is a synthetic, water-soluble tubulin-binding agent with potential antineoplastic activity. Cevipabulin appears to bind at the vinca-binding site on tubulin but seems to act more similar to taxane-site binding agents in that it enhances tubulin polymerization and does not induce tubulin depolymerization. The disruption in microtubule dynamics may eventually inhibit cell division and reduce cellular growth.

Originator

Curator's Comment: # Wyeth Holdings Corp

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
582 ng/mL
31.5 mg/m² 1 times / week multiple, intravenous
dose: 31.5 mg/m²
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
CEVIPABULIN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
2768 ng × h/mL
31.5 mg/m² 1 times / week multiple, intravenous
dose: 31.5 mg/m²
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
CEVIPABULIN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
27.2 h
31.5 mg/m² 1 times / week multiple, intravenous
dose: 31.5 mg/m²
route of administration: Intravenous
experiment type: MULTIPLE
co-administered:
CEVIPABULIN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
31.5 mg/m2 1 times / week multiple, intravenous
Highest studied dose
Dose: 31.5 mg/m2, 1 times / week
Route: intravenous
Route: multiple
Dose: 31.5 mg/m2, 1 times / week
Sources: Page: p.268
unhealthy, ADULT
n = 7
Health Status: unhealthy
Condition: cancer
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Population Size: 7
Sources: Page: p.268
DLT: Febrile neutropenia...
Disc. AE: Neutropenia...
Dose limiting toxicities:
Febrile neutropenia (14.3%)
AEs leading to
discontinuation/dose reduction:
Neutropenia (grade 3-4, 42.9%)
Sources: Page: p.268
AEs

AEs

AESignificanceDosePopulation
Febrile neutropenia 14.3%
DLT
31.5 mg/m2 1 times / week multiple, intravenous
Highest studied dose
Dose: 31.5 mg/m2, 1 times / week
Route: intravenous
Route: multiple
Dose: 31.5 mg/m2, 1 times / week
Sources: Page: p.268
unhealthy, ADULT
n = 7
Health Status: unhealthy
Condition: cancer
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Population Size: 7
Sources: Page: p.268
Neutropenia grade 3-4, 42.9%
Disc. AE
31.5 mg/m2 1 times / week multiple, intravenous
Highest studied dose
Dose: 31.5 mg/m2, 1 times / week
Route: intravenous
Route: multiple
Dose: 31.5 mg/m2, 1 times / week
Sources: Page: p.268
unhealthy, ADULT
n = 7
Health Status: unhealthy
Condition: cancer
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Population Size: 7
Sources: Page: p.268
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer

Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no

Sample Use Guides

Patients were treated with TTI-237 (Cevipabulin) intravenously on days 1, 8 and 15 of a 28-day cycle at dose of 4.5, 9, 15, 22.5 and 31.5 mg/m2 .
Route of Administration: Intravenous
HeLa cells were harvested by trypsinization, washed, counted, and distributed to wells of 96-well flat-bottomed microtiter plates at 1,000 cells per well in 200 AL of medium. All plates were incubated at 37C in humidified 5% CO2 in air for ~24 h. On day 2, compounds for test were diluted and added to wells. Compounds were dissolved in DMSO at 10 to 20 mkmol/L. For each compound, nine serial 2-fold dilutions were prepared in DMSO. Ten microliters of each dilution was transferred to 100 mkL of medium and mixed well, and then 5 AL of this dilution were transferred in triplicate or quadruplicate to wells containing cells. The final high concentration of each compound was typically 5 mkmol/L. All cultures, including controls with no compound, contained a final concentration of 0.27% DMSO. After 3 d of culture with test compounds (day 5 overall), the MTS assay (Promega; CellTiter 96 aqueous nonradioactive cell proliferation assay) was done on all wells.
Name Type Language
CEVIPABULIN
INN   WHO-DD  
INN  
Official Name English
cevipabulin [INN]
Common Name English
Cevipabulin [WHO-DD]
Common Name English
TTI-237
Code English
Classification Tree Code System Code
NCI_THESAURUS C67422
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
NCI_THESAURUS C25974
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
Code System Code Type Description
DRUG BANK
DB12533
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
NCI_THESAURUS
C77064
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
PUBCHEM
11488110
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
INN
8812
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID00233997
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
SMS_ID
300000034113
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
FDA UNII
P14M0DWS2J
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
MESH
C521494
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL1182714
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY
CAS
849550-05-6
Created by admin on Fri Dec 15 15:41:12 GMT 2023 , Edited by admin on Fri Dec 15 15:41:12 GMT 2023
PRIMARY