Structure Database (LMSD)

Common Name
tuberculosinol
Systematic Name
(2E)-3-methyl-5-[(1R,2S,8aS)-1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-1-yl]pent-2-en-1-ol
Synonyms
  • halima-5,6-dien-15-ol
LM ID
LMPR0104030005
Formula
C20H34O
Exact Mass
Calculate m/z
290.260965
Status
Active
Show lipids differing only in stereochemistry/bond geometry

Main

Classification

Category
Main Class
Sub Class
Level 4 Class
Prenol Lipids [PR]
Isoprenoids [PR01]
C20 isoprenoids (diterpenes) [PR0104]
Labdane and halimane diterpenoids [PR010403]

String Representations

InChiKey (Click to copy)
VHFDWNJLUATPID-AHKHSGQUSA-N
InChi (Click to copy)
InChI=1S/C20H34O/c1-15(11-14-21)10-13-20(5)16(2)8-9-17-18(20)7-6-12-19(17,3)4/h9,11,16,18,21H,6-8,10,12-14H2,1-5H3/b15-11+/t16-,18+,20+/m0/s1
SMILES (Click to copy)
C1[C@]2([H])C(=CC[C@H](C)[C@]2(CC/C(/C)=C/CO)C)C(C)(C)CC1

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Mycobacterium tuberculosis H37Rv (#83332)
Actinomycetia (#1760)
Mycobacterium tuberculosis H37Rv3377c encodes the diterpene cyclase for producing the halimane skeleton.,
Chem Commun (Camb), 2005
Pubmed ID: 15719101

Other Databases

CHEBI ID
50387
PubChem CID
24883452
SwissLipids ID
SLM:000390232

Calculated Physicochemical Properties

Heavy Atoms 21
Rings 2
Aromatic Rings 0
Rotatable Bonds 4
Van der Waals Molecular Volume 333.35
Topological Polar Surface Area 20.23
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 1
logP 5.79
Molar Refractivity 91.66

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Updated at
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