24,25-dihydrolanosterol is a 3beta-sterol formed from lanosterol by reduction across the C-24C-25 double bond.
Definition
24,25-dihydrolanosterol is a 3beta-sterol formed from lanosterol by reduction across the C-24C-25 double bond. It has a role as a mouse metabolite and a human metabolite. It is a tetracyclic triterpenoid and a 3beta-sterol. It is functionally related to a lanosterol.
Source: PubChem
US FDA substance register · UNII 9H273A8B2X · registered name DIHYDROLANOSTEROL · single chemical substance
Cosmetic roles
Safety & regulatory references
Other restriction: ban substances that deplete the ozone layer
Source: EU CosIng ingredient list
More data — names, identifiers, properties, test records, literature
Official labels & definitions
JCIA labelling name ジヒドロラノステロール: 本品は、次の化学式で表されるステロールである。
Source: JCIA labelling names (Japan)
Names & identifiers
- CAS No.chemical registry number
- 79-62-9
- DTXSIDUS EPA chemical ID
- DTXSID101000181
- DTXCIDUS EPA compound ID
- DTXCID801427148
- IUPAC
- Lanost-8-en-3beta-ol
- Molecular formula
- C30H52O
- Molecular weight
- 428.745 g/mol
Measured properties
- Appearance
- Solid
Values measured on the substance itself, not a specification for a commercial raw material.
Source: PubChem
What products actually use it for
What the 3 products reported to the US EPA with this ingredient use it for. Products outside cosmetics are included, so the top few rows are its main uses.
- Emulsifier2
- Softener and conditioner1
Source: US EPA CompTox dashboard
Related literature
- The Potential of Isoprenoids in Adjuvant Cancer Therapy to Reduce Adverse Effects of Statins · 2019
- Study of supercritical CO2 extraction of tamarillo (Cyphomandra Betacea) seed oil containing high added value compounds · 2018
- Abstract 5098: Targeting the cholesterol pathway geneSC4MOLsensitizes cancer to EGFR inhibitors · 2010
- Crystal structure of cytochrome P450 14α-sterol demethylase (CYP51) from Mycobacterium tuberculosis in complex with azole inhibitors · 2001
- Calmodulin antagonists suppress cholesterol synthesis by inhibiting sterol Δ24 reductasereductase · 1987
Linked databases 16
- ChEBI
- ChEMBL
- China inventory of existing ingredients (IECIC)
- EU CosIng ingredient list 2
- JCIA labelling names (Japan)
- Korea Cosmetic Association ingredient dictionary
- MFDS (Korea) cosmetic ingredient register 2
- PubChem 2
- Tlooto literature search 2 3 4 5
- UniChem cross-reference IDs
- US EPA CompTox dashboard 2
- US EPA DSSTox chemical database
- US FDA substance registration (GSRS)
- US FDA Unique Ingredient Identifier (UNII)
- Wikidata
- Wikipedia · English · Chinese