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Details

Stereochemistry ACHIRAL
Molecular Formula C7H10NO7P2.Na
Molecular Weight 305.0941
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RISEDRONATE SODIUM

SMILES

[Na+].OC(CC1=CN=CC=C1)(P(O)(O)=O)P(O)([O-])=O

InChI

InChIKey=DRFDPXKCEWYIAW-UHFFFAOYSA-M
InChI=1S/C7H11NO7P2.Na/c9-7(16(10,11)12,17(13,14)15)4-6-2-1-3-8-5-6;/h1-3,5,9H,4H2,(H2,10,11,12)(H2,13,14,15);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C7H10NO7P2
Molecular Weight 282.1043
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: https://www.drugs.com/mtm/risedronate.html http://www.wikidoc.org/index.php/Risedronate http://www.rxlist.com/actonel-drug.htm

Risedronic acid is a pyridinyl bisphosphonate that inhibits osteoclast-mediated bone resorption and modulates bone metabolism. The action of risedronate on bone tissue is based partly on its affinity for hydroxyapatite, which is part of the mineral matrix of bone. Risedronate also targets farnesyl pyrophosphate (FPP) synthase. It is FDA approved for the treatment of postmenopausal osteoporosis, osteoporosis in men, glucocorticoid-induced osteoporosis and Paget’s disease. Calcium, antacids, or oral medications containing divalent cations interfere with the absorption of Risedronic acid. Common adverse reactions include rash, abdominal pain, constipation, diarrhea, indigestion, nausea, backache, urinary tract infectious disease and influenza-like illness.

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ACTONEL

Approved Use

ACTONEL is indicated for the treatment and prevention of osteoporosis and Paget’s disease of bone in men and women.

Launch Date

1998
Primary
ACTONEL

Approved Use

ACTONEL is indicated for the treatment and prevention of glucocorticoid-induced osteoporosis in men and women who are either initiating or continuing systemic glucocorticoid treatment (daily dosage of ≥ 7.5 mg prednisone or equivalent) for chronic diseases.

Launch Date

1998
Primary
ACTONEL

Approved Use

ACTONEL is indicated for treatment of Paget’s disease of bone in men and women.

Launch Date

1998
Primary
ACTONEL

Approved Use

ACTONEL is indicated for treatment to increase bone mass in men with osteoporosis.

Launch Date

1998
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
2.05 ng/mL
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RISEDRONATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
6.49 ng × h/mL
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RISEDRONATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.61 h
5 mg single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RISEDRONATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
The efficacy and tolerability of risedronate once a week for the treatment of postmenopausal osteoporosis.
2002-08
Activity of bisphosphonates against Trypanosoma brucei rhodesiense.
2002-07-04
Bone quality: getting closer to a definition.
2002-07
Risedronate preserves trabecular architecture and increases bone strength in vertebra of ovariectomized minipigs as measured by three-dimensional microcomputed tomography.
2002-07
Sequential treatment with basic fibroblast growth factor and PTH is more efficacious than treatment with PTH alone for increasing vertebral bone mass and strength in osteopenic ovariectomized rats.
2002-07
The potential of parathyroid hormone as a therapy for osteoporosis.
2002-06-26
Treatment of postmenopausal osteoporosis.
2002-06-08
Do bisphosphonates reduce the risk of osteoporotic fractures? An evaluation of the evidence to date.
2002-05-28
Osteoporosis in men.
2002-05-25
The bisphosphonate zoledronic acid impairs Ras membrane [correction of impairs membrane] localisation and induces cytochrome c release in breast cancer cells.
2002-05-06
Gateways to clinical trials.
2002-05
Risedronate: a new oral bisphosphonate.
2002-05
The cost utility of bisphosphonate treatment in established osteoporosis.
2002-05
[Episcleritis secondary to risedronate].
2002-04-27
[When osteoporosis first manifests itself. Without therapy the next fracture threatens].
2002-04-04
[Osteoporosis - Evidence based therapy].
2002-04
Risedronate for the prevention of fractures in postmenopausal osteoporosis.
2002-04
[Risedronate, a new diphosphonate in osteoporosis and Paget's disease].
2002-03-02
[Risedronate: clinical usage].
2002-03
Risedronate for the prevention and treatment of corticosteroid-induced osteoporosis.
2002-03
Upper gastrointestinal tract safety of risedronate: a pooled analysis of 9 clinical trials.
2002-03
Antiresorptive treatment of postmenopausal osteoporosis: comparison of study designs and outcomes in large clinical trials with fracture as an endpoint.
2002-02
Risedronate treatment and extended fracture protection in postmenopausal women.
2002-01-17
Medical treatment of osteoporosis--increasing options.
2002-01
Therapies to improve bone mineral density and reduce the risk of fracture: clinical trial results.
2002-01
Risedronate reduces the risk of first vertebral fracture in osteoporotic women.
2002
The underuse of therapy in the secondary prevention of hip fractures.
2002
Actions of bisphosphonates in animal models of breast cancer.
2002
Development of bisphosphonates.
2002
Direct effects of bisphosphonates on breast cancer cells.
2002
Effect of vitamin D on bone mineral density of elderly patients with osteoporosis responding poorly to bisphosphonates.
2002
[Therapy of osteoporosis. Risk factors alone are not an indication].
2001-12-06
Risedronate for the prevention and treatment of postmenopausal osteoporosis: results from recent clinical trials.
2001-12
Bisphosphonates for the treatment of postmenopausal osteoporosis: clinical studies of etidronate and alendronate.
2001-12
Review of risedronate in the treatment of osteoporosis.
2001-12
Anabolic agents for treating postmenopausal osteoporosis.
2001-12
Inhibition of bone resorption by alendronate and risedronate does not require osteoclast apoptosis.
2001-12
[Economic aspects of osteoporosis therapy. What does a prevented fracture cost?].
2001-11-22
A method to assess the proportion of treatment effect explained by a surrogate endpoint.
2001-11-15
[Alternatives to hormonal treatment for the prevention of postmenopausal osteoporosis: the bisphosphonates].
2001-11
Bisphosphonate treatment suppresses not only stochastic remodeling but also the targeted repair of microdamage.
2001-11
The role of serial bone mineral density testing for osteoporosis.
2001-11
Role of alendronate and risedronate in preventing and treating osteoporosis.
2001-11
[Osteoporosis. Fracture as alarm signal].
2001-10-11
Tolerability of risedronate in postmenopausal women intolerant of alendronate.
2001-10
Risedronate increases bone density and reduces vertebral fracture risk within one year in men on corticosteroid therapy.
2001-10
Alendronate for the treatment of osteoporosis in men.
2001-10
Paget's disease of the spine and its management.
2001-10
Ocular adverse effects of alendronic acid.
2001-06
Comparison insight dual X-ray absorptiometry (DXA), histomorphometry, ash weight, and morphometric indices for bone evaluation in an animal model (the orchidectomized rat) of male osteoporosis.
2001-01
Patents

Sample Use Guides

Treatment of Postmenopausal Osteoporosis: 5 mg daily, 35 mg once-a-week, 75 mg two consecutive days each month, 150 mg once-a-month. Prevention of Postmenopausal Osteoporosis: 5 mg daily, 35 mg once-a-week. Men with Osteoporosis: 35 mg once-a-week. Glucocorticoid-Induced Osteoporosis: 5 mg daily. Paget’s Disease: 30 mg daily for 2 month.
Route of Administration: Oral
The antimalarial activities of risedronate, one of the most potent bisphosphonates clinically used to treat bone resorption diseases, against blood stages of Plasmodium falciparum (50% inhibitory concentration [IC50] of 20.3±1.0 μM).
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:13:16 GMT 2025
Edited
by admin
on Mon Mar 31 18:13:16 GMT 2025
Record UNII
OFG5EXG60L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RISEDRONATE SODIUM ANHYDROUS
Preferred Name English
RISEDRONATE SODIUM
MART.   ORANGE BOOK   USAN   USP   VANDF   WHO-DD  
USAN  
Official Name English
RISEDRONATE SODIUM [USP-RS]
Common Name English
Risedronate sodium [WHO-DD]
Common Name English
NSC-722598
Code English
NSC-759280
Code English
RISEDRONATE SODIUM [MART.]
Common Name English
NE-58095 ANHYDROUS
Code English
RISEDRONATE SODIUM [ORANGE BOOK]
Common Name English
PHOSPHONIC ACID, (1-HYDROXY-2-(3-PYRIDINYL)ETHYLIDENE)BIS-, MONOSODIUM SALT
Common Name English
RISEDRONATE SODIUM [VANDF]
Common Name English
RISEDRONATE MONOSODIUM
Common Name English
RISEDRONIC ACID MONOSODIUM SALT [MI]
Common Name English
RISEDRONATE SODIUM [USAN]
Common Name English
RISEDRONATE SODIUM [USP MONOGRAPH]
Common Name English
Sodium trihydrogen [1-hydroxy-2-(3-pyridyl)ethylidene]diphosphonate
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C443
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
NCI_THESAURUS C67439
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
FDA ORPHAN DRUG 229106
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
Code System Code Type Description
PUBCHEM
68739
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
ChEMBL
CHEMBL923
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
NCI_THESAURUS
C1528
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
NSC
722598
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
USAN
AA-96
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
EPA CompTox
DTXSID1046132
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
EVMPD
SUB04252MIG
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
SMS_ID
100000092051
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
EVMPD
SUB129792
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
DRUG BANK
DBSALT000494
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
RXCUI
60334
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY RxNorm
DAILYMED
OFG5EXG60L
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
FDA UNII
OFG5EXG60L
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
CAS
115436-72-1
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
NSC
759280
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
RS_ITEM_NUM
1604610
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY
MERCK INDEX
m9630
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
PRIMARY Merck Index
RXCUI
1926958
Created by admin on Mon Mar 31 18:13:16 GMT 2025 , Edited by admin on Mon Mar 31 18:13:16 GMT 2025
ALTERNATIVE
Related Record Type Details
SOLVATE->ANHYDROUS
PARENT -> SALT/SOLVATE
SOLVATE->ANHYDROUS
SUBSTANCE->BASIS OF STRENGTH
BASIS OF STRENGTH->SUBSTANCE
on the dried basis for the monohydrate form or on the anhydrous basis for the hemi-pentahydrate form
ASSAY (HPLC)
USP
Related Record Type Details
IMPURITY -> PARENT
UNSPECIFIED
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
molecular weight of risedronate related compound B as a free acid, 530.20
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
UNSPECIFIED
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY