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Fosamprenavir Calcium

HCID 131535
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
226700-81-8
Standard SMILES
CC(C)CN(C[C@@H](OP(=O)([O-])[O-])[C@H](Cc1ccccc1)NC(=O)O[C@H]1CCOC1)S(=O)(=O)c1ccc(N)cc1.[Ca+2]
InChIKey
PMDQGYMGQKTCSX-HQROKSDRSA-L
Molecular formula
C25H34CaN3O9PS
Average molar mass
623.7 g/mol
Monoisotopic mass
623.13792828

Overview

Fosamprenavir is a prescription medicine approved by the U.S. Food and Drug Administration (FDA) for the treatment of HIV in adults and children. Fosamprenavir is always used in combination with other HIV medicines.

Names & identifiers

Preferred name
Fosamprenavir Calcium
IUPAC
calcium [(2R,3S)-1-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-3-[[(3S)-oxolan-3-yl]oxycarbonylamino]-4-phenylbutan-2-yl] phosphate
English name
Fosamprenavir calcium
Molecular formula
C25H36N3O9PS.Ca
Molecular weight
625.69

Names & synonyms

Fosamprenavir calcium226700-81-8Fosamprenavir Calcium SaltLexivaTelzirGW 433908GDTXSID0046777GW433908GGW-433908GID1GU2627NDTXCID8026777RefChem:55231
Show more names
FOSAMPRENAVIRGW-43390820-Fosanavitamin CalciumFOSAMPRENAVIR, CALCIUM SALTFosamprenavir Calcium (200 mg)Fosamprenavir Calcium (GW433908G)
Fosamprenavir (Calcium Salt)Fosamprenavir calcium [USAN]Calcium (2R,3S)-1-(4-amino-N-isobutylphenylsulfonamido)-4-phenyl-3-(((((S)-tetrahydrofuran-3-yl)oxy)carbonyl)amino)butan-2-yl phosphatecalcium;[(2R,3S)-1-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-3-[[(3S)-oxolan-3-yl]oxycarbonylamino]-4-phenylbutan-2-yl] phosphateCAS-226700-81-8MFCD08141843Carbamic acid, ((1S,2R)-3-(((4-aminophenyl)sulfonyl)(2-methylpropyl)amino)-1-(phenylmethyl)-2-(phosphonooxy)propyl)-, C-((3S)-tetrahydro-3-furanyl) ester, calcium salt (1:1)Fosamprenavir calcium (USAN)

Database identifiers

CAS
226700-81-8
PubChem CID
131535
DTXSID

Properties

Computed structural properties

Topological polar surface area
192 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
11
Rotatable bonds
13
Heavy atoms
40
Formal charge
0
Complexity
901

Experimental & physicochemical properties

Human Drugs · 3 items

Breast Feeding; Lactation; Milk, Human; Anti-Infective Agents; Antiviral Agents; Anti-HIV Agents; Anti-Retroviral Agents; HIV Protease Inhibitors

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Physicochemical properties

Melting point
282 · 282-2840C
storage temp.
-20 °C · Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility
Aqueous Acid (Slightly), DMF (Slightly)
form
Solid
color
White to Off-White
BCS Class
2 · 2
InChIKey
PMDQGYMGQKTCSX-HQROKSDRSA-L
SMILES
[O-]P(O[C@H](CN(CC(C)C)S(C1=CC=C(N)C=C1)(=O)=O)[C@@H](NC(O[C@@H]2COCC2)=O)CC3=CC=CC=C3)([O-])=O.[Ca+2]
FDA UNII
1 GU2627N · ID1GU2627N
ATC code
5 AE07 · J05AE07
UNSPSC Code
41116107 · 41116107

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 · 4 items

Warning

H315 (33.3%): Causes skin irritation [Warning Skin corrosion/irritation]

P203, P260, P263, P264, P270, P280, P302+P352, P318, P319, P321, P332+P317, P362+P364, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 3 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Hazard Classes and CategoriesCarc. 2 (66.7%)

Toxicology

Drug Induced Liver Injury · 6 items

Drug Induced Liver Injury Rank (DILIrank 2.0)

Fosamprenavir calcium

Ambiguous-DILI-concern

3

Warnings & precautions

DOI:10.1016/j.drudis.2016.02.015

Effects During Pregnancy and Lactation◉ Summary of Use during Lactation

Safety data

wgk
WGK 3
Signal word
Warning
Symbol(GHS)
GHS08,GHS07
Storage Class
11 - Combustible Solids
Hazard statements
H315-H361
Precautionary statements
P264-P280-P302+P352-P321-P332+P313-P362-P201-P202-P281-P308+P313-P405-P501

Chemistry & industry

Pharmacology

FDA Pharmacological Classification · 2 items

FOSAMPRENAVIR CALCIUM

Cytochrome P450 3A4 Inhibitors [MoA]; P-Glycoprotein Inducers [MoA]; Protease Inhibitor [EPC]; Cytochrome P450 3A4 Inducers [MoA]; HIV Protease Inhibitors [MoA]

MeSH Pharmacological Classification · 2 items

Inhibitors of HIV PROTEASE, an enzyme required for production of proteins needed for viral assembly.

Agents used to treat AIDS and/or stop the spread of the HIV infection. These do not include drugs used to treat symptoms or opportunistic infections associated with AIDS.

Applications · 5 items

DescriptionFosamprenavir (calcium salt) is an orally bioavailable prodrug of the HIV-1 protease inhibitor amprenavir . Fosamprenavir has improved solubility compared with amprenavir, and its pharmacokinetics, either during fasting or with a low- or high-fat meal, suggest that it could be effective using fewer tablets and a less complex dosing schedule than other HIV treatments. Formulations containing fosamprenavir are used for adult and pediatric patients with HIV infection, especially as an initial antiretroviral therapy.

DescriptionFosamprenavir, a prodrug of the HIV protease inhibitor amprenavir, is indicated for the oral treatment of HIV infection in adults in combination with other antiretroviral agents. Although amprenavir has excellent antiviral potency and good tolerability, its watersolubility is poor (0.04 mg/ml). As a result, the formulation of the agent includes a high percentage of organic excipients to facilitate gastric dissolution, which limits the amount of active drug that can be formulated per capsule. Fosamprenavir is a highly soluble phosphate ester of amprenavir. It allows more convenient dosing and reduction in pill counts as compared to amprenavir. Fosamprenavir is readily prepared in two steps starting from a key intermediate used in the synthesis of amprenavir, by phosphorylating a hydroxyl group and subsequently reducing a p-nitrophenyl to a p-aminophenyl group. Fosamprenavir has little or no antiviral activity in vitro. After oral administration, it is rapidly and almost completely hydrolyzed by phosphatases in the gut epithelium to amprenavir prior to reaching systemic circulation. The time to reach peak plasma concentration of amprenavir is approximately 2.5 h and the plasma elimination half-life is approximately 7.7 h. Amprenavir is metabolized in the liver by CYP3A4 and >90% of the dose is excreted as metabolites in urine and feces. In most patients, fosamprenavir is administered at daily doses of 700–1400 mg in conjunction with ritonavir. Monotherapy with fosamprenavir is only recommended in antiretroviral therapy-nave patients and the dosing regimen is 1400 mg twice daily. The most common adverse events experienced with fosamprenavir are diarrhea, nausea, vomiting, headache and rash.

Related reactions

3 records
New reaction record
HRID 333034 reaction equation
HRID 333034As productuspto-grants-2014_11
HRID 1526527 reaction equation
HRID 1526527As productuspto-grants-2015_07
HRID 2275407 reaction equation
HRID 2275407As productuspto-grants-2015_09

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
DTXSID0046777
ChEMBL
CHEMBL1200734
UNII
ID1GU2627N
EC Number
607-123-4
NACRES
77 · NA.77
Protein binding
90 · 90 (amprenavir)
Excreted unchanged in urine
1 · <1 (amprenavir)
Volume of distribution
6 · 6 (amprenavir)
Biological half-life
7.7 · 7.7 / Unchanged (amprenavir)
Symbol(GHS)
8 · GHS08,GHS07
Signal word
Warning
Hazard statements
315 · H315-H361
Precautionary statements
264 · P264-P280-P302+P352-P321-P332+P313-P362-P201-P202-P281-P308+P313-P405-P501
WGK Germany
3 · WGK 3
Storage Class
11 · 11 - Combustible Solids

UsesHIV protease inhibitor; water soluble prodrug of amprenavir.

UsesProtease inhibitor, anti-HIV agent

General DescriptionFosamprenavir is used in combination with otherHIV drugs in adult patients. Like the other PIs, this compoundis a prodrug that produces the active drug uponhydrolysis. In this case, the active drug is amprenavir, apeptidomimetic transition state inhibitor. Fosamprenaviris typically administered in combination with RTinhibitors.

Suppliers89 total

北京华美互利生物化工010-56205725 · [email protected]
Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
武汉英诺医药科技有限公司+86-027-59232304 15387063101 · [email protected]
成都超九八生物科技有限公司13348960310 13348960310 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
咸宁深蓝生物医药研发有限公司18171815831 · [email protected]
杭州品高化工有限公司0571-87658025 · [email protected]
上海毕得医药科技股份有限公司400-1647117 13681763483 · [email protected]
湖北科乐精细化工有限公司027-59101668 19945030958 · [email protected]
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]
浙江珲达生物科技有限公司0571-89903022 18679456698 · [email protected]
LGM Pharma1-(800)-881-8210 · [email protected]
Hangzhou Sage Chemical Co., Ltd.+86057186818502 13588463833 · [email protected]
安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]
梯希爱(上海)化工贸易有限公司021-61109150 · [email protected]
欧利希(湖北)医药科技有限公司17316404525 17316404525 · [email protected]
InvivoChem中国13549236410 · [email protected]
MedBio脉铂医药021-69568360 18916172912 · [email protected]
上海相辉医药科技有限公司13761987713; 13761987713 · [email protected]
北京博奥森生物技术有限公司400-901-9800 18611424007 · [email protected]
上海泰坦科技股份有限公司400-6009262 15618770481 · [email protected]
MedChemexpress LLC021-58955995 · [email protected]
Zhejiang J&C Biological Technology Co.,Limited+1-2135480471 · [email protected]
上海瀚香生物科技有限公司177-54423994 17754423994 · [email protected]
杭州东帆化学有限公司86-0571-85151182
AdooQ BioScience, LLC+1 (866) 930-6790 · [email protected]
上海遐瑞医药科技有限公司+86 21 61551611
泰州市众致生物科技有限公司[email protected] 15066129350 · [email protected]
上海诺宝化工有限公司+86(0)21 60484900
湖北威德利化学试剂有限公司186-02735115 18602735115 · [email protected]
Cato Research Chemicals Inc.020-81960175 · [email protected]
PT CHEM GROUP LIMITED+86-85511178; +86-85511178 · [email protected]
雷丁试剂0510-85629785 18013409632 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
南京百鑫德诺生物科技有限公司025-58849295 · [email protected]
Chongqing jooe co., ltd+86-15223382610 · [email protected]
青岛海智微元生物科技有限公司18317699790 18317699790 · [email protected]
凯试(上海)科技有限公司021-50135380 · [email protected]
普善实业(陕西)有限公司029-81310890 18165209495 · [email protected]
上海一研生物科技有限公司021-69985186 13611928337 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
BOC Sciences16314854226; +8616314854226 · [email protected]
厦门志信化学有限公司+86-5922680277 +86-13806087780 · [email protected]
艾吉析科技(上海)有限公司17721401538;17717235263 17721401538 · [email protected]
上海阿拉丁生化科技股份有限公司6206333 13167063860 · [email protected]
武汉多普乐生物医药有限公司+86-02787215551 19945035818 · [email protected]
BOC Sciences16314854226 · [email protected]
Hebei Ningnan Trade Co. LTD+86-18034019111 · [email protected]
药渡经纬信息科技(北京)有限公司+86-400-851-9921 · [email protected]
广州市齐云生物技术有限公司020-61288194 61288195 · [email protected]