Pamidronate Disodium Anhydrous

HCID 73351

データを補完しています。通常は 1 分以内に完了します

基本情報

CAS
57248-88-1
標準SMILES
NCCC(O)(P(=O)([O-])O)P(=O)([O-])O.[Na+].[Na+]
InChIKey
CEYUIFJWVHOCPP-UHFFFAOYSA-L
分子式
C3H9NNa2O7P2
平均分子量
279.03 g/mol
単同位体質量
278.96496345

概要

Pamidronate Disodium is the disodium salt of the synthetic bisphosphonate pamidronate. Although its mechanism of action is not completely understood, pamidronate appears to adsorb to calcium phosphate crystals in bone, blocking their dissolution by inhibiting osteoclast-mediated bone resorption. This agent does not inhibit bone mineralization and formation.

名称と識別子

優先名称
Pamidronate Disodium Anhydrous
IUPAC
disodium;[3-amino-1-hydroxy-1-[hydroxy(oxido)phosphoryl]propyl]-hydroxyphosphinate

名称と別名

PAMIDRONATE DISODIUM57248-88-1Disodium pamidronateAminomuxPamidronic acid disodium saltPamidronate disodium anhydrousC7S8VWP5DHGCP-23339ADTXSID5042667Phosphonic acid, (3-amino-1-hydroxypropylidene)bis-, disodium saltNSC-722600CGP-23339AE
名称をさらに表示
NSC720699RefChem:57112DTXCID3022667260-647-18742T8ZQZACGP 23339AEPamidronate disodium pentahydratePhosphonic acid, (3-amino-1-hydroxypropylidene)bis-, disodium salt, pentahydrate

データベース識別子

CAS
57248-88-1
PubChem CID
73351
DTXSID
DTXSID5042667
ChEMBL
CHEMBL3989401、CHEMBL676
UNII
C7S8VWP5DH
EC Number
260-647-1

物性

構造計算による物性補完中

極性表面積
167 Ų
水素結合供与体数
4
水素結合受容体数
8
回転可能結合数
4
重原子数
15

実験および物理化学的性質

Human Drugs · 2 件

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

安全と法規制

GHS分類

GHS Classification · 4 件

Warning

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

P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P308+P316, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 6 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory InformationPhosphonic acid, (3-amino-1-hydroxypropylidene)bis-, disodium salt: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Hazard Classes and CategoriesAcute Tox. 4 (100%)

毒性情報

TreatmentIf overdosage occurs, symptomatic hypocalcemia could also result; such patients should be treated with short-term intravenous calcium. (L1712)
Health EffectsRare cases of uveitis, iritis, scleritis, and episcleritis have been reported, including one case of scleritis, and one case of uveitis upon separate rechallenges.
Exposure RoutesParenteral (intravenous). Plasma concentration rises rapidly upon IV administration.
Toxicity Summary · 1 件

The mechanism of action of pamidronate is inhibition of bone resorption. Pamidronate adsorbs to calcium phosphate (hydroxyapatite) crystals in bone and may directly block dissolution of this mineral component of bone. In vitro studies also suggest that inhibition of osteoclast activity contributes to inhibition of bone resorption. Pamidronate also targets farnesyl pyrophosphate (FPP) synthase. Nitrogen-containing bisphosphonates (such as pamidronate, alendronate, risedronate, ibandronate and zoledronate) appear to act as analogues of isoprenoid diphosphate lipids, thereby inhibiting FPP synthase, an enzyme in the mevalonate pathway. Inhibition of this enzyme in osteoclasts prevents the biosynthesis of isoprenoid lipids (FPP and GGPP) that are essential for the post-translational farnesylation and geranylgeranylation of small GTPase signalling proteins. This activity inhibits osteoclast activity and reduces bone resorption and turnover. In postmenopausal women, it reduces the elevated rate of bone turnover, leading to, on average, a net gain in bone mass.

Signs and SymptomsSide effects include an allergic reaction, kidney problems, seizures, low levels of calcium, magnesium, or phosphorus in the blood
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).

化学と産業

薬理情報

Metabolism/Metabolites · 1 件

Pamidronate is not metabolized and is exclusively eliminated by renal excretion. Route of Elimination: Pamidronate is not metabolized and is exclusively eliminated by renal excretion. Half Life: The mean ± SD elimination half-life is 28 ± 7 hours

FDA Pharmacological Classification · 2 件

PAMIDRONATE DISODIUM

Diphosphonates [CS]; Bisphosphonate [EPC]

MeSH Pharmacological ClassificationAgents that inhibit BONE RESORPTION and/or favor BONE MINERALIZATION and BONE REGENERATION. They are used to heal BONE FRACTURES and to treat METABOLIC BONE DISEASES such as OSTEOPOROSIS.

用途と製造

Uses · 1 件

Pamidronate is in a class of drugs called bisphosphonates. Pamidronate reduces breakdown of the bones. Pamidronate is used in the treatment of Paget's disease of bone; to reduce high levels of calcium in the blood associated with malignancy (cancer); and to reduce the breakdown of bone due to metastases of breast cancer or multiple myeloma. For the treatment of moderate or severe hypercalcemia associated with malignancy

サプライヤー100 社

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
南通飞宇生物科技有限公司0513-68819626 15152877458 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
成都彼样生物科技有限公司18108052721 · [email protected]

関連反応

5 件

化合物ノート

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