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19356-17-3 molecular structure
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(1R,3Z)-3-{2-[(1R,4E,7aR)-1-[(2R)-6-hydroxy-6-methylheptan-2-yl]-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol

ChemBase ID: 32
Molecular Formular: C27H44O2
Molecular Mass: 400.63706
Monoisotopic Mass: 400.33413065
SMILES and InChIs

SMILES:
OC(CCC[C@H]([C@@H]1[C@@]2(C(CC1)/C(=C/C=C\1/C[C@H](O)CCC1=C)/CCC2)C)C)(C)C
Canonical SMILES:
O[C@@H]1CCC(=C)/C(=C\C=C\2/CCC[C@]3(C2CC[C@@H]3[C@@H](CCCC(O)(C)C)C)C)/C1
InChI:
InChI=1S/C27H44O2/c1-19-10-13-23(28)18-22(19)12-11-21-9-7-17-27(5)24(14-15-25(21)27)20(2)8-6-16-26(3,4)29/h11-12,20,23-25,28-29H,1,6-10,13-18H2,2-5H3/b21-11+,22-12-/t20-,23-,24-,25?,27-/m1/s1
InChIKey:
JWUBBDSIWDLEOM-BNQRRPJDSA-N

Cite this record

CBID:32 http://www.chembase.cn/molecule-32.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(1R,3Z)-3-{2-[(1R,4E,7aR)-1-[(2R)-6-hydroxy-6-methylheptan-2-yl]-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol
IUPAC Traditional name
calcifediol
Brand Name
Calderol
Delakmin
Synonyms
Calcifediol
Calcifediol Anhydrous
Calcifediolum [INN-Latin]
Calcifidiol
Calcidiol
CAS Number
19356-17-3
PubChem SID
160963495
PubChem CID
6433735

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem ALOGPS 2.1
Acid pKa 18.384342  H Acceptors
H Donor LogD (pH = 5.5) 5.654346 
LogD (pH = 7.4) 5.654346  Log P 5.654346 
Molar Refractivity 125.0606 cm3 Polarizability 48.829468 Å3
Polar Surface Area 40.46 Å2 Rotatable Bonds
Lipinski's Rule of Five false 
Log P 6.71  LOG S -5.26 
Solubility (Water) 2.20e-03 g/l 

PROPERTIES

PROPERTIES

Physical Property Bioassay(PubChem)
Solubility
Insoluble expand Show data source
Hydrophobicity(logP)
6 expand Show data source

DETAILS

DETAILS

DrugBank DrugBank
DrugBank - DB00146 external link
Item Information
Drug Groups approved; nutraceutical
Description The major circulating metabolite of vitamin D3 (cholecalciferol). It is produced in the liver and is the best indicator of the body's vitamin D stores. It is effective in the treatment of rickets and osteomalacia, both in azotemic and non-azotemic patients. Calcifediol also has mineralizing properties. [PubChem]
Indication Used to treat vitamin D deficiency or insufficiency, refractory rickets (vitamin D resistant rickets), familial hypophosphatemia and hypoparathyroidism, and in the management of hypocalcemia and renal osteodystrophy in patients with chronic renal failure undergoing dialysis. Also used in conjunction with calcium in the management and prevention of primary or corticosteroid-induced osteoporosis.
Pharmacology Calcidiol is the precursor of vitamin D3. Vitamin D3 is a steroid hormone that has long been known for its important role in regulating body levels of calcium and phosphorus, in mineralization of bone, and for the assimilation of vitamin A. The classical manifestations of vitamin D deficiency is rickets, which is seen in children and results in bony deformaties including bowed long bones. Deficiency in adults leads to the disease osteomalacia. Both rickets and osteomalacia reflect impaired mineralization of newly synthesized bone matrix, and usually result from a combination of inadequate exposure to sunlight and decreased dietary intake of vitamin D. Common causes of vitamin D deficiency include genetic defects in the vitamin D receptor, severe liver or kidney disease, and insufficient exposure to sunlight. Vitamin D plays an important role in maintaining calcium balance and in the regulation of parathyroid hormone (PTH). It promotes renal reabsorption of calcium, increases intestinal absorption of calcium and phosphorus, and increases calcium and phosphorus mobilization from bone to plasma.
Toxicity Bone pain, constipation (especially in children or adolescents), diarrhea, drowsiness, dryness of mouth; headache (continuing), increased thirst, increase in frequency of urination, especially at night, or in amount of urine, irregular heartbeat, itching skin, loss of appetite, metallic taste, muscle pain, nausea or vomiting (especially in children or adolescents), unusual tiredness or weakness.
Affected Organisms
Humans and other mammals
Biotransformation Calcidiol undergoes hydroxylation in the mitochondria of kidney tissue, and this reaction is activated by the renal 25-hydroxyvitamin D3-1-(alpha)-hydroxylase to produce calcitriol (1,25- dihydroxycholecalciferol), the active form of vitamin D3.
Absorption Readily absorbed.
Half Life 288 hours
External Links
Wikipedia
PDRhealth

REFERENCES

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