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Irinotecan Hydrochloride

HCID 74990
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Basic informationNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
100286-90-6
Standard SMILES
CCc1c2c(nc3ccc(OC(=O)N4CCC(N5CCCCC5)CC4)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC.Cl
InChIKey
GURKHSYORGJETM-WAQYZQTGSA-N
Molecular formula
C33H39ClN4O6
Average molar mass
623.1 g/mol
Monoisotopic mass
622.2558127

Names & identifiers

Preferred name
Irinotecan Hydrochloride
IUPAC
[(19S)-10,19-diethyl-19-hydroxy-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4(9),5,7,10,15(20)-heptaen-7-yl] 4-piperidin-1-ylpiperidine-1-carboxylate;hydrochloride
English name
Irinotecan hydrochloride
Molecular formula
C33H39ClN4O6
Molecular weight
623.15

Names & synonyms

Irinotecan hydrochloride100286-90-6CPT 11CamptoCPT-11Camptothecin 11 hydrochlorideDTXSID6045953U 101440EIrinotecan hydrochloride anhydrous06X131E4OE7-Ethyl-10-(4-(1-piperidino)-1-piperidino)carbonyloxy camptothecin hydrochlorideCHEBI:5971
Show more names
IRINOTECAN HCL[1,4′-Bipiperidine]-1′-carboxylic acid, CPT-11,(S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinolin-9-yl esterIrinotecan HCICamptothecin II[1,4'-BIPIPERIDINE]-1'-CARBOXYLIC ACIDCPT-IICTP-11CS-1327
DTXCID4025953irinotecan hydrochloride (anhydrous)NSC-759878DQ-2805U-101440ECPT11IrinomedacIrinotecan hydrochloide

Database identifiers

CAS
100286-90-6、136572-09-3

Properties

Computed structural propertiesFilling in

Topological polar surface area
113 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
8
Rotatable bonds
5
Heavy atoms
44
Formal charge
0
Complexity
1,200

Physicochemical properties

Melting point
250 · 250-256°C (dec.)
Boiling point
257 °C · 257 °C
refractive index
67.7 ° · 67.7 ° (C=1, H2O)
storage temp.
2 · 2-8°C
solubility
20 mg/ml · Soluble in DMSO or DMF at approximately 20mg/ml. Sparingly soluble in aqueous buffers. /n
form
Yellow powder
color
White to yellow
biological source
plant (Fructus camptothecae)
Water Solubility
100 mg/ml · Soluble in DMSO at 100mg/ml. Soluble in water at 25mg/ml with warming
Merck
5091 · 5091
InChIKey
GURKHSYORGJETM-GCUJQDEHNA-N
SMILES
C(C1C2=CC(OC(N3CCC(N4CCCCC4)CC3)=O)=CC=C2N=C2C3=CC4[C@@](C(=O)OCC=4C(=O)N3CC=12)(O)CC)C.Cl |&1:28,r|
CAS DataBase Reference
100286 · 100286-90-6(CAS DataBase Reference)
NCI Dictionary of Cancer Terms
irinotecan hydrochloride

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 5 items

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 41 reports by companies from 1 notifications to the ECHA C&L Inventory.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

Hazard information

Hazard Classes and CategoriesAcute Tox. 4 (100%)

Toxicology

Drug Induced Liver Injury · 6 items

Drug Induced Liver Injury Rank (DILIrank 2.0)

Irinotecan hydrochloride

vLess-DILI-concern

3

Adverse reactions

DOI:10.1016/j.drudis.2016.02.015

Safety data

PPE
dust mask type N95 (US), Eyeshields, Gloves
wgk
3
rtecs
DW1060750
hs_code
29399990
risk_code
22
Signal word
Warning
Symbol(GHS)
GHS07
hazard_code
Xn

Chemistry & industry

Pharmacology

FDA Pharmacological Classification · 4 items

IRINOTECAN HYDROCHLOIDE

Topoisomerase Inhibitor [EPC]; Topoisomerase Inhibitors [MoA]

IRINOTECAN HYDROCHLORIDE

Topoisomerase Inhibitor [EPC]; Topoisomerase Inhibitors [MoA]

MeSH Pharmacological ClassificationCompounds that inhibit the activity of DNA TOPOISOMERASE I.

Uses & manufacturing

UsesUse (kg; approx.) in Germany (2009): >25;Use (kg) in USA (2002): 24;Consumption (g per capita; approx.) in Germany (2009): 0.000305;Consumption (g per capita) in the USA (2002): 8.51e-05;Calculated removal (%): 13.3
Applications · 5 items

Descriptionlrinotecan hydrochloride, a semi-synthetic, water soluble derivative of the potent anticancer agent camptothecin, was launched in Japan for the treatment of lung, ovarian, and cervical cancers. lrinotecan exerts its antitumor activity via inhibition of topoisomerase I, a cellular enzyme that is involved in maintaining the topographic structure of DNA during the process of translation, transcription, and mitosis. lrinotecan undergoes de-esterification in vivo to yield an active metabolite, SN-38, which is 1000-fold more potent than the parent. Although being much less toxic than camptothecin, a significant number of patients in clinical trials exhibited side effects of leukopenia, diarrhea, nauseahromiting, and alopecia. Combination therapy of irinotecan with another widely used anticancer agent, cisplatin, has been reported to be superior to either agent alone. lrinotecan is in clinical trials for gastrointestinal, breast, skin, colorectal, pancreatic cancers, mesothelioma and non-Hodgkin's lymphoma.

Usesantineoplactic;'inhibitor of topoisomerase I

UsesIrinotecan hydrochloride has been used:in combination with 5-fluorouracil for screening growth inhibitory functionality in MDA-MB-231 breast cancer cells.in chemosensitivity screening of high-grade appendiceal (HGA) and low-grade appendiceal (LGA) organoids.as a chemotherapeutic agent in the cytotoxicity studies in combination with heat shock proteins inhibitors (HPSC1) in HT29 colon cancer cells.

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Related reactions

1 records
New reaction record
HRID 1724885 reaction equation
HRID 1724885As productuspto-grants-2009_02

Compound notes

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On this pageBasic informationNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
PubChem CID
74990
DTXSID
DTXSID6045953
ChEMBL
CHEMBL3989514、CHEMBL541887
ChEBI
CHEBI:5971
UNII
06X131E4OE
EC Number
600-054-0
FDA UNII
6 X131E4OE · 06X131E4OE
NCI Drug Dictionary
irinotecan hydrochloride
UNSPSC Code
12352204 · 12352204
NACRES
77 · NA.77
Protein binding
65 % · 65%
Excreted unchanged in urine
20 % · 20%
Volume of distribution
110 · 110-234 Litres/m2(L/kg)
Biological half-life
14 · 14 / -
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
302 · H302
Precautionary statements
264 · P264-P270-P301+P312a-P330-P501a
PPE
95 · dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes
Xn
Risk Statements
22 · 22
WGK Germany
3 · 3
RTECS
1060750 · DW1060750
HS Code
29399990 · 29399990
Storage Class
11 · 11 - Combustible Solids
Hazard Classifications
4 Oral · Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
Hazard statements
H302
Hazard Classifications
Acute Tox. 4 Oral
Precautionary statements
P264-P270-P301+P312a-P330-P501a

UsesA DNA topoisomerase inhibitor

General DescriptionIrinotecan is available in 100-mg or 5-mL vials for IV administrationand is used in combination with 5-FU and leucovorinas first-line treatment of metastatic colon cancer.The agent may also be used as a single agent in colorectalcancer as a second-line therapy when 5-FU therapy hasfailed. Additional uses include small cell lung cancer,NSCLC, cervical cancer, esophageal cancer, and gastric cancer Irinotecan is 30% to 60% plasma protein bound, whereasthe active metabolite SN-38 is 95% protein bound. Bindingof SN-38 as the lactone stabilizes the material to ring opening.The elimination of the agent occurs primarily in the bilewith a minor amount of renal elimination. The excretion ofactive metabolites or inactive metabolites such as the glucuronideSN-38G, which may be converted back to SN-38 inthe bile, has been associated with severe diarrhea. Irinotecanand SN-38 have half-lives of 8 and 14 hours, respectively.Irinotecan has two dose-limiting toxicities, myelosuppressionand diarrhea. The diarrhea occurs in two forms, earlyand late. The early form occurs within the first 24 hours afteradministration. It has been associated with inhibition ofacetylcholinesterase, which results in increased gut motility.This early phase is also associated with flushing, abdominalpain, and excessive sweating. Atropine can be used to relievethese symptoms but it is not recommended for prophylacticuse unless there has been a prior episode. The late-phasediarrhea occurs after 24 hours and has been associated withthe presence of active material, particularly SN-38 in the gut,and may last 3 to 10 days. The prolonged nature may lead todehydration and electrolyte imbalances. Loperamide therapyis recommended at the first appearance of a loose stool. If thediarrhea persists, additional agents may be used includingantibiotics that decrease β-glucosidase–producing bacteria inthe gut and prevent the overgrowth of pathogenic bacteria.111Other toxicities include emesis and alopecia.

Upstream & downstream products

Upstream raw materials

Triethylamine7-Ethyl-10-hydroxycamptothecin1,4-Butenediol4-Piperidinopiperidine1-(5-Hydroxy-2-nitrophenyl)-1-propanone1-(2-Amino-5-hydroxyphenyl)propan-1-one1-(5-Fluoro-2-nitrophenyl)propan-1-one1-Chlorocarbonyl-4-piperidinopiperidine(S)-4-Ethyl-4-hydroxy-7,8-dihydro-1h-pyrano[3,4-f]indolizine-3,6,10(4h)-trione3-Fluorobenzaldehyde

Downstream products

Irinotecan hydrochloride trihydrate
Additional notes · 1 item

DefinitionChEBI: A hydrochloride obtained by combining irinotecan with one molar equivalent of hydrochloric acid. Used (in the form of its trihydrate) in combination with fluorouracil and leucovorin, for the treatment of patients with metastatic adenocarcinoma of the pancr as after disease progression following gemcitabine-based therapy. It is converted via hydrolysis of the carbamate linkage to its active metabolite, SN-38, which is ~1000 times more active.