Page last updated: 2024-12-07

1,25-dihydroxyergocalciferol

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

1,25-dihydroxyvitamin D3, also known as calcitriol, is the biologically active form of vitamin D. It is not the same as 1,25-dihydroxyergocalciferol, which is the biologically active form of vitamin D2. However, they are both important for research as they are involved in various biological processes.

Here's a breakdown:

**1,25-dihydroxyvitamin D3 (Calcitriol)**

* **Formation:** Produced in the kidneys from vitamin D3 (cholecalciferol) through a series of enzymatic steps.
* **Function:** Acts as a hormone, regulating calcium and phosphorus metabolism, bone health, and immune function.
* **Importance in research:**
* **Bone health:** Investigating its role in osteoporosis and other bone disorders.
* **Immune system:** Exploring its effects on autoimmune diseases and infections.
* **Cancer:** Studying its potential in preventing or treating certain cancers.
* **Cardiovascular disease:** Examining its impact on blood pressure, heart health, and inflammation.
* **Other diseases:** Researching its involvement in conditions like diabetes, multiple sclerosis, and inflammatory bowel disease.

**1,25-dihydroxyergocalciferol**

* **Formation:** Produced from vitamin D2 (ergocalciferol) through a similar enzymatic process as calcitriol.
* **Function:** Similar to calcitriol, it regulates calcium and phosphorus metabolism and has various other physiological roles.
* **Importance in research:** While not as widely studied as calcitriol, it's important for understanding:
* **Differences in vitamin D2 and D3 metabolism:** Researchers are investigating how their differing structures and biological activities might affect health outcomes.
* **Nutritional implications:** As vitamin D2 is commonly found in fortified foods, its research helps assess its efficacy compared to vitamin D3.

**In Summary:**

* Both calcitriol and 1,25-dihydroxyergocalciferol are crucial for understanding the role of vitamin D in various biological processes.
* Calcitriol, being the active form of vitamin D3, is more commonly studied, while 1,25-dihydroxyergocalciferol research focuses on the unique aspects of vitamin D2 and its potential health benefits.

Research on these compounds continues to advance our understanding of vitamin D's role in maintaining health and developing potential treatments for various diseases.

1,25-dihydroxyergocalciferol: RN given refers to (3beta,5Z,7E,22E)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1alpha,25-dihydroxyvitamin D2 : A hydroxycalciol that is vitamin D2 bearing additional hydroxy substituents at positions 1alpha and 25. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID9547243
CHEMBL ID4303615
CHEBI ID86320
SCHEMBL ID264875
MeSH IDM0044598

Synonyms (47)

Synonym
LMST03010040
(5z,7e,22e)-(1s,3r)-9,10-seco-5,7,10(19),22-ergostatetraene-1,3,25-triol
1alpha,25-dihydroxyvitamin d2 / 1alpha,,25-dihydroxyergocalciferol
HY-32350
ercalcitriol ,
1alpha,25-dihydroxyvitamin d2, >=97.0% (sum of vitamin and previtamin, hplc)
1,25-dihydroxyergocalciferol
1,25-dihydroxy vitamin d
1,25-dihydroxyvitamin d2
1alpha,25-dihydroxyvitamin d2
60133-18-8
CS-0394
ro 17-6218
1,25-dihydroxycalciferol
SCHEMBL264875
5RWP08OQ36 ,
ro-17-6218
1,3-cyclohexanediol, 4-methylene-5-((2e)-2-((1r,3as,7ar)-octahydro-1-((1r,2e)-5-hydroxy-1,4,5-trimethyl-2-hexen-1-yl)-7a-methyl-4h-inden-4-ylidene)ethylidene)-, (1r,3s,5z)-
unii-5rwp08oq36
1.alpha.,25-dihydroxyergocalciferol
9,10-secoergosta-5,7,10(19),22-tetraene-1,3,25-triol, (1alpha,3beta,5z,7e,22e)-
1.alpha.,25-dihydroxyvitamin d2
9,10-secoergosta-5,7,10(19),22-tetraene-1,3,25-triol, (1.alpha.,3.beta.,5z,7e,22e)-
1alpha,25-dihydroxyergocalciferol
(1r,3s,5z)-4-methylene-5-[(2e)-2-[(1r,3as,7ar)-octahydro-1-[(1r,2e)-5-hydroxy-1,4,5-trimethyl-2-hexen-1-yl]-7?-methyl-4h-inden-4-ylidene]ethylidene]-1,3-cyclohexanediol
1?,25-dihydroxyvitamin d2
25-hydroxy doxercalciferol
DTXSID90429509
1alpha,25-dihydroxycalciferol
CHEBI:86320
AKOS024457904
1a,25-dihydroxycalciferol
1a,25-dihydroxyergocalciferol
1a,25-dihydroxyvitamin d2
o-1h-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol
(1r,3s,5z)-5-[(2e)-2-[(1r,3as,7ar)-1-[(e,2r,5s)-5,6-dimethyl-6-oxidanyl-hept-3-en-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydr
ZGLHBRQAEXKACO-XJRQOBMKSA-N
Q27159080
1-alpha,25-dihydroxyvitamin d2
CHEMBL4303615
9,10-secoergosta-5,7,10(19),22-tetraene-1,3,25-triol,(1a,3b,5z,7e,22e)-
EX-A4431
(1r,3s,5z)-5-[(2e)-2-[(1r,3as,7ar)-1-[(e,2r,5s)-6-hydroxy-5,6-dimethylhept-3-en-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1h-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol
1 alpha ,25-dihydroxyvitamin d2
A869040
AS-75822
1(alpha) 25-dihydroxyvitamin d2*

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Active and less toxic vitamin D analogs could be useful for clinical applications."( Toxicity and antitumor activity of the vitamin D analogs PRI-1906 and PRI-1907 in combined treatment with cyclophosphamide in a mouse mammary cancer model.
Filip, B; Kutner, A; Milczarek, M; Nevozhay, D; Wietrzyk, J, 2008
)
0.35
"The LD50 values after five daily subcutaneous (s."( Toxicity and antitumor activity of the vitamin D analogs PRI-1906 and PRI-1907 in combined treatment with cyclophosphamide in a mouse mammary cancer model.
Filip, B; Kutner, A; Milczarek, M; Nevozhay, D; Wietrzyk, J, 2008
)
0.35

Dosage Studied

ExcerptRelevanceReference
" Time-course and dose-response studies on 1,25-(OH)(2)D(3) and 19-nor-1,25-(OH)(2)D(2) induction of the marker of bone formation, osteocalcin, showed overlapping curves."( Relative potencies of 1,25-(OH)(2)D(3) and 19-Nor-1,25-(OH)(2)D(2) on inducing differentiation and markers of bone formation in MG-63 cells.
Dusso, AS; Finch, JL; Pavlopoulos, T; Slatopolsky, EA, 2001
)
0.31
"Mice were randomized into treatment and control groups for 5-week toxicity and dose-response studies."( Toxicity and dose-response studies of 1alpha-hydroxyvitamin D2 in a retinoblastoma xenograft model.
Albert, DM; Bryar, PJ; Darjatmoko, SR; Grostern, RJ; Lindstrom, MJ; Lissauer, BJ; Lokken, JM; Strugnell, SA; Zimbric, ML, 2002
)
0.31
"2 microg/d were selected on the basis of toxicity studies for the dose-response trial."( Toxicity and dose-response studies of 1alpha-hydroxyvitamin D2 in a retinoblastoma xenograft model.
Albert, DM; Bryar, PJ; Darjatmoko, SR; Grostern, RJ; Lindstrom, MJ; Lissauer, BJ; Lokken, JM; Strugnell, SA; Zimbric, ML, 2002
)
0.31
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
bone density conservation agentAn agent that inhibits bone resorption and/or favor bone mineralization and bone regeneration. Used to heal bone fractures and to treat bone diseases such as osteopenia and osteoporosis.
human xenobiotic metaboliteAny human metabolite produced by metabolism of a xenobiotic compound in humans.
nutraceuticalA product in capsule, tablet or liquid form that provide essential nutrients, such as a vitamin, an essential mineral, a protein, an herb, or similar nutritional substance.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (3)

ClassDescription
hydroxycalciol
seco-ergostane
vitamin DAny member of a group of fat-soluble hydroxy seco-steroids that exhibit biological activity against vitamin D deficiency. Vitamin D can be obtained from sun exposure, food and supplements and is biologically inactive and converted into the biologically active calcitriol via double hydroxylation in the body.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (121)

TimeframeStudies, This Drug (%)All Drugs %
pre-199040 (33.06)18.7374
1990's28 (23.14)18.2507
2000's17 (14.05)29.6817
2010's35 (28.93)24.3611
2020's1 (0.83)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials6 (4.92%)5.53%
Reviews8 (6.56%)6.00%
Case Studies6 (4.92%)4.05%
Observational0 (0.00%)0.25%
Other102 (83.61%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]