Metabolite

KNApSAcK Entry

id C00023747
Name 7-Dehydrocholesterol / Provitamin D3,Cholesta-5,7-dien-3beta-ol
CAS RN 434-16-2
Standard InChI InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9-10,18-19,21,23-25,28H,6-8,11-17H2,1-5H3/t19-,21+,23-,24+,25+,26+,27-/m1/s1
Standard InChI (Main Layer) InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9-10,18-19,21,23-25,28H,6-8,11-17H2,1-5H3

Cluster

Phytochemical cluster No. 11
KCF-S cluster No. 111

Link

ChEMBL

By standard InChI CHEMBL1797131
By standard InChI Main Layer CHEMBL1480760 CHEMBL1797131

KEGG

By LinkDB C01164

CTD

By CAS RN C016705

Human Protein / Gene in interaction

5 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P11473 Vitamin D3 receptor NR1I1 CHEMBL1480760 CHEMBL1794311 (1) CHEMBL1963865 (1)
CHEMBL1963915 (1) CHEMBL1963934 (1)
2 / 3
O00255 Menin Unclassified protein CHEMBL1480760 CHEMBL1614531 (1)
2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme CHEMBL1480760 CHEMBL1614531 (1)
1 / 3
Q13951 Core-binding factor subunit beta Unclassified protein CHEMBL1480760 CHEMBL1613933 (1)
0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein CHEMBL1480760 CHEMBL1613933 (1)
1 / 6

CTD interaction (2)

compound gene gene name gene description interaction interaction type form reference
pmid
C016705 1717 DHCR7
SLOS
7-dehydrocholesterol reductase (EC:1.3.1.21) DHCR7 mutant form results in increased abundance of 7-dehydrocholesterol increases abundance
mutant form 16446309
C016705 1717 DHCR7
SLOS
7-dehydrocholesterol reductase (EC:1.3.1.21) DHCR7 results in increased reduction of 7-dehydrocholesterol increases reduction
15896653

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (13)

KEGG disease name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)

Diseases related to CTD interactions

1 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D019082 C016705 Smith-Lemli-Opitz Syndrome marker/mechanism
11254748