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Inulin
Inulin is an unknown pharmaceutical. Inulin was first approved as Inulin and sodium chloride on 1982-01-01.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Inulin
Tradename
Company
Number
Date
Products
INULIN AND SODIUM CHLORIDEIso-Tex DiagnosticsN-002282 DISCN1982-01-01
1 products
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Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
V: Various drug classes in atc
— V04: Diagnostic agents
— V04C: Other diagnostic agents in atc
— V04CH: Renal function and ureteral injuries test diagnostic agents
— V04CH01: Inulin and other polyfructosans
HCPCS
No data
Clinical
Clinical Trials
130 clinical trials
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Mock data
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Patent ductus arteriosusD004374HP_0001643Q25.01551415
PancreatitisD010195EFO_0000278K85——44513
Premature obstetric laborD007752O602323311
Healthy volunteers/patients—3——216
Postoperative painD010149G89.18—12115
Ankylosing spondylitisD013167EFO_0003898M45——11—2
Colorectal neoplasmsD0151791——1—2
HemorrhageD006470MP_0001914R58——11—2
InflammationD0072491——1—2
Premature birthD047928EFO_0003917O60—1—1—2
Show 10 more
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Squamous cell carcinoma of head and neckD000077195—21——3
Cardiovascular diseasesD002318EFO_0000319I98111——2
Squamous cell carcinomaD002294—11——2
Cerebral intraventricular hemorrhageD000074042111——2
Gouty arthritisD015210——1——1
Langerhans-cell histiocytosisD006646C96.6—11——1
PainD010146EFO_0003843R52——1——1
Renal colicD056844EFO_1001412N23——1——1
Alzheimer diseaseD000544EFO_0000249F03——1——1
Congenital heart defectsD006330HP_0001627Q24.9——1——1
Show 2 more
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Prostatic neoplasmsD011471C6133———4
Regional blood flowD012039—1——12
AdenocarcinomaD000230—1———1
Covid-19D000086382U07.111———1
HypertensionD006973EFO_0000537I1011———1
StrokeD020521EFO_0000712I63.911———1
Obstructive sleep apneaD020181EFO_0003918G47.3311———1
Dental pinsD003772—1———1
TachycardiaD013610HP_0001649R00.011———1
Orthostatic intoleranceD05497111———1
Show 11 more
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
AsthmaD001249EFO_0000270J451————1
Ovarian neoplasmsD010051EFO_0003893C561————1
Esophageal neoplasmsD004938C151————1
Pure autonomic failureD0549701————1
Orthostatic hypotensionD007024I95.11————1
Drug interactionsD0043471————1
Breast neoplasmsD001943EFO_0003869C501————1
Triple negative breast neoplasmsD0647261————1
Male breast neoplasmsD0185671————1
GoutD006073EFO_0004274M101————1
Show 1 more
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Nephrogenic diabetes insipidusD018500N25.1————11
Endoscopic retrograde cholangiopancreatographyD002760————11
Migraine disordersD008881EFO_0003821G43————11
Acute necrotizing pancreatitisD019283————11
DehydrationD003681E86.0————11
Wounds and injuriesD014947T14.8————11
Ocular physiological phenomenaD009799————11
PancreaticoduodenectomyD016577————11
Systemic inflammatory response syndromeD018746EFO_1001478R65.10————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameINULIN
INN—
Description
Inulins are a group of naturally occurring polysaccharides produced by many types of plants, industrially most often extracted from chicory. The inulins belong to a class of dietary fibers known as fructans. Inulin is used by some plants as a means of storing energy and is typically found in roots or rhizomes. Most plants that synthesize and store inulin do not store other forms of carbohydrate such as starch. In the United States in 2018, the Food and Drug Administration approved inulin as a dietary fiber ingredient used to improve the nutritional value of manufactured food products. Using inulin to measure kidney function is the "gold standard" for comparison with other means of estimating glomerular filtration rate.
Classification
Small molecule
Drug class—
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
OC[C@H]1O[C@H](O[C@]2(CO[C@]3(CO[C@]4(CO[C@]5(CO[C@]6(CO[C@]7(CO[C@]8(CO[C@]9(CO[C@]%10(CO[C@]%11(CO[C@]%12(CO[C@]%13(CO[C@]%14(CO[C@]%15(CO[C@]%16(CO[C@]%17(CO[C@]%18(CO[C@]%19(CO[C@]%20(CO[C@]%21(CO[C@]%22(CO[C@]%23(CO[C@]%24(CO[C@]%25(CO[C@]%26(CO[C@]%27(CO[C@]%28(CO[C@]%29(CO[C@]%30(CO[C@]%31(CO[C@]%32(CO[C@]%33(CO[C@]%34(CO[C@]%35(CO[C@]%36(CO[C@]%37(CO[C@]%38(CO)O[C@H](CO)[C@@H](O)[C@@H]%38O)O[C@H](CO)[C@@H](O)[C@@H]%37O)O[C@H](CO)[C@@H](O)[C@@H]%36O)O[C@H](CO)[C@@H](O)[C@@H]%35O)O[C@H](CO)[C@@H](O)[C@@H]%34O)O[C@H](CO)[C@@H](O)[C@@H]%33O)O[C@H](CO)[C@@H](O)[C@@H]%32O)O[C@H](CO)[C@@H](O)[C@@H]%31O)O[C@H](CO)[C@@H](O)[C@@H]%30O)O[C@H](CO)[C@@H](O)[C@@H]%29O)O[C@H](CO)[C@@H](O)[C@@H]%28O)O[C@H](CO)[C@@H](O)[C@@H]%27O)O[C@H](CO)[C@@H](O)[C@@H]%26O)O[C@H](CO)[C@@H](O)[C@@H]%25O)O[C@H](CO)[C@@H](O)[C@@H]%24O)O[C@H](CO)[C@@H](O)[C@@H]%23O)O[C@H](CO)[C@@H](O)[C@@H]%22O)O[C@H](CO)[C@@H](O)[C@@H]%21O)O[C@H](CO)[C@@H](O)[C@@H]%20O)O[C@H](CO)[C@@H](O)[C@@H]%19O)O[C@H](CO)[C@@H](O)[C@@H]%18O)O[C@H](CO)[C@@H](O)[C@@H]%17O)O[C@H](CO)[C@@H](O)[C@@H]%16O)O[C@H](CO)[C@@H](O)[C@@H]%15O)O[C@H](CO)[C@@H](O)[C@@H]%14O)O[C@H](CO)[C@@H](O)[C@@H]%13O)O[C@H](CO)[C@@H](O)[C@@H]%12O)O[C@H](CO)[C@@H](O)[C@@H]%11O)O[C@H](CO)[C@@H](O)[C@@H]%10O)O[C@H](CO)[C@@H](O)[C@@H]9O)O[C@H](CO)[C@@H](O)[C@@H]8O)O[C@H](CO)[C@@H](O)[C@@H]7O)O[C@H](CO)[C@@H](O)[C@@H]6O)O[C@H](CO)[C@@H](O)[C@@H]5O)O[C@H](CO)[C@@H](O)[C@@H]4O)O[C@H](CO)[C@@H](O)[C@@H]3O)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
Identifiers
PDB—
CAS-ID9005-80-5
RxCUI5924
ChEMBL IDCHEMBL1201646
ChEBI ID—
PubChem CID24763
DrugBankDB00638
UNII ID—
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 25,473 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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5,305 adverse events reported
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