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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6O4.Pt.2H3N
Molecular Weight 371.254
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBOPLATIN

SMILES

N.N.[Pt++].[O-]C(=O)C1(CCC1)C([O-])=O

InChI

InChIKey=OLESAACUTLOWQZ-UHFFFAOYSA-L
InChI=1S/C6H8O4.2H3N.Pt/c7-4(8)6(5(9)10)2-1-3-6;;;/h1-3H2,(H,7,8)(H,9,10);2*1H3;/q;;;+2/p-2

HIDE SMILES / InChI
Carboplatin is an organoplatinum compound that possesses antineoplastic activity. Carboplatin is an intravenously administered platinum coordination complex and alkylating agent, which is used as a chemotherapeutic agent for the treatment of various cancers, mainly of advanced ovarian. Carboplatin is indicated for the palliative treatment of patients with ovarian carcinoma recurrent after prior chemotherapy, including patients who have been previously treated with cisplatin. In addition this drug can be used to treat others cancers. Carboplatin therapy is associated with a low rate of transient serum aminotransferase elevations and with rare instances of clinically apparent liver injury. Carboplatin, like cisplatin, produces predominantly interstrand DNA cross-links rather than DNA-protein cross-links. This effect is apparently cell-cycle nonspecific. The aquation of carboplatin, which is thought to produce the active species, occurs at a slower rate than in the case of cisplatin. Despite this difference, it appears that both carboplatin and cisplatin induce equal numbers of drug-DNA cross-links, causing equivalent lesions and biological effects.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: CHEMBL2311221
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CARBOPLATIN

Approved Use

Initial Treatment of Advanced Ovarian Carcinoma: Carboplatin injection is indicated for the initial treatment of advanced ovarian carcinoma in established combination with other approved chemotherapeutic agents. One established combination regimen consists of carboplatin and cyclophosphamide. Two randomized controlled studies conducted by the NCIC and SWOG with carboplatin versus cisplatin, both in combination with cyclophosphamide, have demonstrated equivalent overall survival between the two groups. There is limited statistical power to demonstrate equivalence in overall pathologic complete response rates and long-term survival (≥3 years) because of the small number of patients with these outcomes: the small number of patients with residual tumor <2 cm after initial surgery also limits the statistical power to demonstrate equivalence in this subgroup. Secondary Treatment of Advanced Ovarian Carcinoma. Carboplatin is indicated for the palliative treatment of patients with ovarian carcinoma recurrent after prior chemotherapy, including patients who have been previously treated with cisplatin. Within the group of patients previously treated with cisplatin, those who have developed progressive disease while receiving cisplatin therapy may have a decreased response rate.

Launch Date

1.17737285E12
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
38.99 μg/mL
375 mg/m² single, intravenous
dose: 375 mg/m²
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CARBOPLATIN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
197.71 μg × h/mL
375 mg/m² single, intravenous
dose: 375 mg/m²
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CARBOPLATIN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
39.81 h
375 mg/m² single, intravenous
dose: 375 mg/m²
route of administration: Intravenous
experiment type: SINGLE
co-administered:
CARBOPLATIN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
100%
CARBOPLATIN plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
550 mg/m2 1 times / 4 weeks multiple, intraperitoneal
Dose: 550 mg/m2, 1 times / 4 weeks
Route: intraperitoneal
Route: multiple
Dose: 550 mg/m2, 1 times / 4 weeks
Sources:
unhealthy, 54.2 years (range: 36.9-77.3 years)
n = 47
Health Status: unhealthy
Condition: ovarian carcinoma
Age Group: 54.2 years (range: 36.9-77.3 years)
Sex: F
Population Size: 47
Sources:
600 mg/m2 single, intravenous
MTD
Dose: 600 mg/m2
Route: intravenous
Route: single
Dose: 600 mg/m2
Sources:
unhealthy, 60 years (range: 21 - 80 years)
n = 2
Health Status: unhealthy
Age Group: 60 years (range: 21 - 80 years)
Sex: M+F
Population Size: 2
Sources:
Other AEs: Thrombocytopenia...
Other AEs:
Thrombocytopenia (2 patients)
Sources:
160 mg/m2 1 times / week multiple, intravenous
Highest studied dose
Dose: 160 mg/m2, 1 times / week
Route: intravenous
Route: multiple
Dose: 160 mg/m2, 1 times / week
Sources:
unhealthy, > 60 years
n = 93
Health Status: unhealthy
Condition: ovarian carcinoma
Age Group: > 60 years
Sex: F
Population Size: 93
Sources:
210 mg/m2 1 times / week multiple, intravenous
MTD
Dose: 210 mg/m2, 1 times / week
Route: intravenous
Route: multiple
Dose: 210 mg/m2, 1 times / week
Sources:
unhealthy, children
Health Status: unhealthy
Condition: solid tumors
Age Group: children
Sex: M+F
Sources:
AEs

AEs

AESignificanceDosePopulation
Thrombocytopenia 2 patients
600 mg/m2 single, intravenous
MTD
Dose: 600 mg/m2
Route: intravenous
Route: single
Dose: 600 mg/m2
Sources:
unhealthy, 60 years (range: 21 - 80 years)
n = 2
Health Status: unhealthy
Age Group: 60 years (range: 21 - 80 years)
Sex: M+F
Population Size: 2
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG



OverviewOther

Drug as perpetrator​Drug as victim
PubMed

PubMed

TitleDatePubMed
Increased DNA-binding activity of cis-1,1-cyclobutanedicarboxylatodiammineplatinum(II) (carboplatin) in the presence of nucleophiles and human breast cancer MCF-7 cell cytoplasmic extracts: activation theory revisited.
1999 Nov 15
Patents

Patents

Sample Use Guides

Single-Agent Therapy: Carboplatin injection, as a single agent, has been shown to be effective in patients with recurrent ovarian carcinoma at a dosage of 360 mg/m2 IV on day 1 every 4 weeks. In general, however, single intermittent courses of carboplatin should not be repeated until the neutrophil count is at least 2,000 and the platelet count is at least 100,000. Combination Therapy with Cyclophosphamide: In the chemotherapy of advanced ovarian cancer, an effective combination for previously untreated patients consists of: Carboplatin―300 mg/m2 IV on day 1 every 4 weeks for 6 cycles. Cyclophosphamide―600 mg/m2 IV on day 1 every 4 weeks for 6 cycles.
Route of Administration: Intravenous
Ovarian cancer cell lines (n=36) were treated with carboplatin, cisplatin, paclitaxel, or carboplatin-paclitaxel (CPTX). For each cell line, IC(50) levels were quantified and pre-treatment gene expression analyses were performed. Drug dilutions initially consisted of 1.5-fold serial dilutions from a maximum concentration of 100 μℳ. The cells were incubated with the drug for 72 h to ensure all cell lines underwent a minimum of two doublings. It was found, that characterisation of gene expression signatures in ovarian cancer (OVCA) patients may be useful for characterisng responses to treatment and also in developing an understanding of the biology that drives clinical outcome and survival. Furthermore, it was identified BAD, APC/C, and CREB was key players in the cytotoxicity of carboplatin, cisplatin, and paclitaxel in OVCA cell lines, and was suggested that targeted therapies against regulators of these proteins may be worthy of study in chemoresistant OVCAs.
Name Type Language
CARBOPLATIN
EP   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
NSC-201345
Code English
carboplatin [INN]
Common Name English
CARBOPLATIN [HSDB]
Common Name English
PLATINUM, DIAMINE(1,1-CYCLOBUTANEDICARBOXYLATO (2-)-O,O')-, (SP-4-2)-
Common Name English
CARBOPLATIN [ORANGE BOOK]
Common Name English
CARBOPLATIN [EP MONOGRAPH]
Common Name English
CARBOPLATIN [VANDF]
Common Name English
CARBOPLATIN [USP-RS]
Common Name English
PARAPLATIN
Brand Name English
CARBOPLATIN [USAN]
Common Name English
cis-Diammine(1,1-cyclobutanedicarboxylato)platinum
Common Name English
Carboplatin [WHO-DD]
Common Name English
CARBOPLATIN [JAN]
Common Name English
CARBOPLATIN [MI]
Common Name English
CARBOPLATIN [USP MONOGRAPH]
Common Name English
CARBOPLATINUM
Brand Name English
CARBOPLATIN [EP IMPURITY]
Common Name English
NSC-241240
Code English
CARBOPLATIN [MART.]
Common Name English
CARBOPLATIN [USP IMPURITY]
Common Name English
Classification Tree Code System Code
LIVERTOX NBK548565
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 8.2
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
WHO-VATC QL01XA02
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
NDF-RT N0000175073
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
EU-Orphan Drug EU/3/18/2043
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
WHO-ATC L01XA02
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
NCI_THESAURUS C1450
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
NDF-RT N0000175413
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
Code System Code Type Description
LACTMED
Carboplatin
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
HSDB
6957
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
RS_ITEM_NUM
1096407
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PRIMARY
FDA UNII
BG3F62OND5
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
MESH
D016190
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
WIKIPEDIA
Carboplatin
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
USAN
T-23
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
RXCUI
40048
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY RxNorm
NSC
241240
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
NSC
201345
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
SMS_ID
100000092564
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
DAILYMED
BG3F62OND5
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL1351
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
IUPHAR
7624
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
EVMPD
SUB06614MIG
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
INN
5231
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
NCI_THESAURUS
C1282
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
DRUG CENTRAL
4133
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
PUBCHEM
10339178
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
CHEBI
31355
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
DRUG BANK
DB00958
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
CHEBI
35690
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
ECHA (EC/EINECS)
255-446-0
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY
MERCK INDEX
m3093
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY Merck Index
CAS
41575-94-4
Created by admin on Sat Dec 16 17:15:53 UTC 2023 , Edited by admin on Sat Dec 16 17:15:53 UTC 2023
PRIMARY