GOLVATINIB TARTRATE

Investigational

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C33H37F2N7O4.C4H6O6
Molecular Weight	783.775
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

O[C@H]([C@@H](O)C(O)=O)C(O)=O.CN1CCN(CC1)C2CCN(CC2)C(=O)NC3=CC(OC4=CC=C(NC(=O)C5(CC5)C(=O)NC6=CC=C(F)C=C6)C(F)=C4)=CC=N3

InChI

InChIKey=JYFKDBFPRXMUAM-LREBCSMRSA-N

InChI=1S/C33H37F2N7O4.C4H6O6/c1-40-16-18-41(19-17-40)24-9-14-42(15-10-24)32(45)39-29-21-26(8-13-36-29)46-25-6-7-28(27(35)20-25)38-31(44)33(11-12-33)30(43)37-23-4-2-22(34)3-5-23;5-1(3(7)8)2(6)4(9)10/h2-8,13,20-21,24H,9-12,14-19H2,1H3,(H,37,43)(H,38,44)(H,36,39,45);1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI

Molecular Formula	C33H37F2N7O4
Molecular Weight	633.6882
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C4H6O6
Molecular Weight	150.0868
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25278451 | https://www.ncbi.nlm.nih.gov/pubmed/24371262
Curator's Comment: Description was created based on several sources, including https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=640626 https://www.ncbi.nlm.nih.gov/pubmed/19832844

Golvatinib is a highly potent, small-molecule, ATP-competitive inhibitor of c-Met and multiple members of the Eph receptor family plus c-Kit and Ron. Eisai was developing an oral formulation of golvatinib, which acts as both a c-Met inhibitor and a vascular endothelial growth factor receptor 2 antagonist with potential antineoplastic activity. Golvatinib binds to and inhibits the activities of both c-Met and VEGFR-2, which may inhibit tumor cell growth and survival of tumor cells that overexpress these receptor tyrosine kinases. c-Met and VEGFR-2 are upregulated in a variety of various tumor cell types and play important roles in tumor cell growth, migration and angiogenesis. Clinical trials involving several forms of cancer are currently underway.

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Hepatocyte growth factor receptor 56 Target ID: CHEMBL3717 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19832844 \| https://www.ncbi.nlm.nih.gov/pubmed/25082515	Inhibitor 8504		20.0 nM [IC50]
Vascular endothelial growth factor receptor 2 112 Target ID: CHEMBL279 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19832844 \| https://www.ncbi.nlm.nih.gov/pubmed/25082515	Antagonist 2849		40.0 nM [IC50]

Conditions

Condition	Modality	Highest Phase	Product
Hepatocellular carcinoma 83 Sources: https://clinicaltrials.gov/ct2/show/NCT01271504	Primary	Phase II 1147	Unknown Approved Use Unknown
Head and neck squamous cell carcinoma 32 Sources: https://clinicaltrials.gov/ct2/show/NCT01332266	Primary	Phase II 1147	Unknown Approved Use Unknown
Gastric cancer 53 Sources: https://clinicaltrials.gov/ct2/show/NCT01355302	Primary	Phase II 1147	Unknown Approved Use Unknown

C_max

Value	Dose	Co-administered	Analyte	Population
9730 ng/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/25278451	400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered:		GOLVATINIB plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED

AUC

Value	Dose	Co-administered	Analyte	Population
171000 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25278451	400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered:		GOLVATINIB plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED
171000 ng × h/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/25278451	400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered:		GOLVATINIB plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED

T_1/2

Value	Dose	Co-administered	Analyte	Population
45 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/25278451	400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered:		GOLVATINIB plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED
45 h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/25278451	400 mg 1 times / day steady-state, oral dose: 400 mg route of administration: Oral experiment type: STEADY-STATE co-administered:		GOLVATINIB plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED

Doses

Dose	Population	Adverse events
450 mg 1 times / day multiple, oral Highest studied dose Dose: 450 mg, 1 times / day Route: oral Route: multiple Dose: 450 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: FASTED Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	DLT: Fatigue, Fatigue... Disc. AE: Vomiting... Dose limiting toxicities: Fatigue (grade 2, 50%) Fatigue (grade 3, 50%) AEs leading to discontinuation/dose reduction: Vomiting (50%) Sources: https://pubmed.ncbi.nlm.nih.gov/25278451
200 mg 2 times / day multiple, oral MTD Dose: 200 mg, 2 times / day Route: oral Route: multiple Dose: 200 mg, 2 times / day Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079
400 mg 1 times / day multiple, oral MTD Dose: 400 mg, 1 times / day Route: oral Route: multiple Dose: 400 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: FASTED Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	Disc. AE: Fatigue, Anorexia... AEs leading to discontinuation/dose reduction: Fatigue (12.5%) Anorexia (12.5%) Sources: https://pubmed.ncbi.nlm.nih.gov/25278451
300 mg 2 times / day multiple, oral Studied dose Dose: 300 mg, 2 times / day Route: oral Route: multiple Dose: 300 mg, 2 times / day Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	DLT: ALT increased... Other AEs: Vomiting, Nausea... Dose limiting toxicities: ALT increased (grade 3, 50%) Other AEs: Vomiting (grade 2, 50%) Nausea (grade 2, 50%) Anorexia (grade 2, 50%) Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079

AEs

AE	Significance	Dose	Population
Vomiting	50% Disc. AE	450 mg 1 times / day multiple, oral Highest studied dose Dose: 450 mg, 1 times / day Route: oral Route: multiple Dose: 450 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: FASTED Sources: https://pubmed.ncbi.nlm.nih.gov/25278451
Fatigue	grade 2, 50% DLT, Disc. AE	450 mg 1 times / day multiple, oral Highest studied dose Dose: 450 mg, 1 times / day Route: oral Route: multiple Dose: 450 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: FASTED Sources: https://pubmed.ncbi.nlm.nih.gov/25278451
Fatigue	grade 3, 50% DLT, Disc. AE	450 mg 1 times / day multiple, oral Highest studied dose Dose: 450 mg, 1 times / day Route: oral Route: multiple Dose: 450 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: FASTED Sources: https://pubmed.ncbi.nlm.nih.gov/25278451
Anorexia	12.5% Disc. AE	400 mg 1 times / day multiple, oral MTD Dose: 400 mg, 1 times / day Route: oral Route: multiple Dose: 400 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: FASTED Sources: https://pubmed.ncbi.nlm.nih.gov/25278451
Fatigue	12.5% Disc. AE	400 mg 1 times / day multiple, oral MTD Dose: 400 mg, 1 times / day Route: oral Route: multiple Dose: 400 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25278451	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: FASTED Sources: https://pubmed.ncbi.nlm.nih.gov/25278451
Anorexia	grade 2, 50%	300 mg 2 times / day multiple, oral Studied dose Dose: 300 mg, 2 times / day Route: oral Route: multiple Dose: 300 mg, 2 times / day Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079
Nausea	grade 2, 50%	300 mg 2 times / day multiple, oral Studied dose Dose: 300 mg, 2 times / day Route: oral Route: multiple Dose: 300 mg, 2 times / day Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079
Vomiting	grade 2, 50%	300 mg 2 times / day multiple, oral Studied dose Dose: 300 mg, 2 times / day Route: oral Route: multiple Dose: 300 mg, 2 times / day Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079
ALT increased	grade 3, 50% DLT	300 mg 2 times / day multiple, oral Studied dose Dose: 300 mg, 2 times / day Route: oral Route: multiple Dose: 300 mg, 2 times / day Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M+F Food Status: UNKNOWN Sources: https://ascopubs.org/doi/abs/10.1200/jco.2012.30.15_suppl.3079

Overview

CYP3A4	CYP2C9	CYP2D6	hERG
inhibitor 2252	inhibitor 2438	inhibitor 2507

OverviewOther

Other Inhibitor	Other Substrate	Other Inducer
P-gp 1741

Drug as perpetrator

Target	Modality	Activity
CYP2C9 2497	inhibitor 4027 Sources: https://pubchem.ncbi.nlm.nih.gov/bioassay/1645842#sid=363680153	inconclusive [IC50 21.3174 uM]
P-gp 1932	inhibitor 4027 Sources: https://pubchem.ncbi.nlm.nih.gov/bioassay/1346987#sid=363680153	inconclusive [IC50 25.929 uM]
CYP2D6 2546	inhibitor 4027 Sources: https://pubchem.ncbi.nlm.nih.gov/bioassay/1645840#sid=363680153	inconclusive [IC50 6.7412 uM]
CYP3A4 2633	inhibitor 4027 Sources: https://pubchem.ncbi.nlm.nih.gov/bioassay/1645841#sid=363680153	yes [IC50 26.837 uM]

PubMed

Title	Date	PubMed
Paracrine receptor activation by microenvironment triggers bypass survival signals and ALK inhibitor resistance in EML4-ALK lung cancer cells.	2012-07-01	22553343
E7050: a dual c-Met and VEGFR-2 tyrosine kinase inhibitor promotes tumor regression and prolongs survival in mouse xenograft models.	2010-01	19832844

Patents

Sample Use Guides

In Vivo Use Guide

Golvatinib at the MTD of 400 mg once daily was well tolerated with pharmacodynamic evidence of c-Met target modulation.

Route of Administration: Oral

In Vitro Use Guide

Golvatinib strongly inhibits the growth of MKN45, EBC-1, Hs746T, and SNU-5 tumor cells with IC50 values of 37, 6.2, 23, and 24 nM, respectively

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:55:55 GMT 2025` Edited by `admin` on `Mon Mar 31 20:55:55 GMT 2025`
Record UNII	47S9L68C0N
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

GOLVATINIB TARTRATE

Official Name

English

ER-396901-08

Preferred Name

English

GOLVATINIB TARTRATE [USAN]

Common Name

English

Golvatinib tartrate [WHO-DD]

Common Name

English

1,1-CYCLOPROPANEDICARBOXAMIDE, N-(2-FLUORO-4-((2-(((4-(4-METHYL-1-PIPERAZINYL)-1-PIPERIDINYL)CARBONYL)AMINO)-4-PYRIDINYL)OXY)PHENYL)-N'-(4-FLUOROPHENYL)-, (2R,3R)-2,3-DIHYDROXYBUTANEDIOATE (1:1)

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID80143505