OralParenteralDosed ingredientTherapeutic flag Cosmetic cross-reference

Ergocalciferol

CAS 50-14-6

Ergocalciferol (CAS 50-14-6) is a Phase 4 pharmaceutical compound with 3 bioactivity targets and 9,306 adverse event associations.

SOURCE NLM DailyMed
Label records
2
SOURCE EMBL-EBI ChEMBL
Bioactivity
8
SOURCE DrugCentral
Adverse signals
9,306
SOURCE IUPHAR/BPS
PubMed IDs
0
SOURCE EMBL-EBI ChEMBL B25820EEF0F0

Compound Identity

Matched identifiers and naming fields for the pharmaceutical compound record.

Primary Name
Ergocalciferol
CAS Number
50-14-6
UNII
VS041H42XC
InChIKey
MECHNRXZTMCUDQ-RKHKHRCZSA-N
ChEMBL ID
CHEMBL1536
Molecule Type
Small molecule
Source Match
EMBL-EBI ChEMBL (INCHIKEY)
dosed ingredientnatural productoralparenteraltherapeutic flag
SOURCE EMBL-EBI ChEMBL B25820EEF0F0

Clinical Development Phase

Highest clinical development phase rendered from the matched compound identifier rows.

Phase 4 (Approved)
Approved or marketed human pharmaceutical use is represented in the source phase field.
ChEMBL CHEMBL1536 | Small molecule
SOURCE Ingredients table / CosIng profile same-CAS cross-reference

Cross-Reference to Cosmetics

Same-CAS ingredient record found in the cosmetics vertical.

SOURCE NLM DailyMed 2 label rows

Drug Label Active Ingredients

Active ingredient and active moiety rows from source drug product labels.

ProductIngredient Active MoietyEffective
Ergocalciferol ERGOCALCIFEROL
VS041H42XC
ERGOCALCIFEROL 20260505
Ergocalciferol ERGOCALCIFEROL
VS041H42XC
ERGOCALCIFEROL 20260505
SOURCE EMBL-EBI ChEMBL 8 bioactivity rows

Bioactivity & Target Interactions

Target-level activity records with assay counts, activity type, and measured value where present.

TargetActivity ValueAssaysOrganism
- AC50 28688.582142857143 nM 28 -
- Potency 28742.55 nM 12 -
- IC50 57800 nM 6 -
- GI50 66850 nM 2 -
- EC50 3800 nM 1 -
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial
Enzyme
- - - Homo sapiens
Vitamin D3 receptor
Nuclear hormone receptor
AGONIST - - Homo sapiens
Vitamin D 25-hydroxylase
Enzyme
- - - Homo sapiens
SOURCE DrugCentral 80 associations

Adverse Event Associations

DrugCentral / FAERS disproportionality signal rows matched to this compound.

Reaction PTDrug AE LLRMedDRA
Toxicity to various agents 543 1711.884 10070863
Completed suicide 200 1042.492 10010144
Drug interaction 1059 975.343 10013710
Drug abuse 114 785.93 10013654
Acute kidney injury 1931 665.02 10069339
Product dose omission issue 4366 635.672 10084406
Multiple sclerosis relapse 1294 623.99 10048393
Fatigue 12375 622.575 10016256
Intentional overdose 76 579.592 10022523
Overdose 418 576.927 10033295
Muscle spasms 2928 457.409 10028334
Thrombocytopenia 1008 429.196 10043554
Back pain 4179 383.588 10003988
Headache 8020 377.835 10019211
Febrile neutropenia 835 349.535 10016288
Multiple organ dysfunction syndrome 257 345.353 10077361
Cardio-respiratory arrest 199 324.099 10007617
Neutropenia 1313 321.805 10029354
Drug ineffective 8289 317.599 10013709
Hepatic function abnormal 86 316.34 10019670
Infective pulmonary exacerbation of cystic fibrosis 449 312.219 10070608
Hypoaesthesia 2669 308.745 10020937
Hypotension 2091 306.285 10021097
Pain in extremity 4617 301.028 10033425
Cardiac arrest 521 298.336 10007515
Cardiac failure 495 297.817 10007554
Suicide attempt 168 288.278 10042464
Depressed level of consciousness 189 279.395 10012373
Hyperkalaemia 279 261.551 10020646
Diarrhoea 9754 259.047 10012735
Fall 5580 251.556 10016173
Multiple sclerosis 612 251.52 10028245
Hyponatraemia 621 248.999 10021036
Sinusitis 2926 248.375 10040753
Memory impairment 1786 247.891 10027175
Rhabdomyolysis 243 245.74 10039020
Drug reaction with eosinophilia and systemic symptoms 81 244.28 10073508
Feeling abnormal 2337 236.771 10016322
Foetal exposure during pregnancy 281 227.237 10071404
Septic shock 394 221.095 10040070
Muscle spasticity 558 220.375 10028335
Pancytopenia 634 217.252 10033661
Electrocardiogram QT prolonged 234 216.903 10014387
Sopor 4 213.013 10058709
Insomnia 3289 210.764 10022437
Interstitial lung disease 365 203.411 10022611
Lactic acidosis 130 203.2 10023676
Respiratory failure 751 197.598 10038695
Metabolic acidosis 191 196.69 10027417
Influenza like illness 1207 194.388 10022004

Association rows are source-linked signal records, not incidence rates or clinical causality claims.

SOURCE NLM RxNorm 3 name rows

Drug Names / RxNorm

Normalized drug-name vocabulary rows, RxCUIs, and source abbreviations.

NameRxCUI TypeSource
Ergocalciferol 4018 SU MTHSPL
ERGOCALCIFEROL 4018 SU MTHSPL
ergocalciferol 4018 IN RXNORM
SOURCE Rendered pharma page rows FAQPage JSON-LD

Frequently Asked Questions

Short answers generated only from the same visible source-linked rows on this page.

What is Ergocalciferol used for in pharmaceutical contexts?

Ergocalciferol (CAS 50-14-6) appears in DailyMed active-ingredient label rows, including Ergocalciferol.

What are the known adverse events for Ergocalciferol?

Ergocalciferol has 9,306 DrugCentral/FAERS adverse event associations. Rendered reaction terms include Toxicity to various agents, Completed suicide, Drug interaction, Drug abuse, Acute kidney injury. Signal rows are source-linked records and should not be read as incidence rates or causality conclusions.

Is Ergocalciferol also used in cosmetics?

Yes. The ingredients table has a same-CAS cosmetic profile for Ergocalciferol with EU status "permitted".

What clinical phase is Ergocalciferol in?

Ergocalciferol is rendered with ChEMBL max phase 4 (approved).

What bioactivity targets are documented for Ergocalciferol?

Ergocalciferol has 8 bioactivity rows in this page query. Rendered target entries include 25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial, Vitamin D3 receptor, Vitamin D 25-hydroxylase.