(1R,4S,5R,7R,10R)-guaiane-1,5,10,11,12-pentaol

Details

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Internal ID f350a8a5-5c11-48fb-a82b-430cac22d6d6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (1S,3aR,4R,7R,8aR)-7-(1,2-dihydroxypropan-2-yl)-1,4-dimethyl-2,3,5,6,7,8-hexahydro-1H-azulene-3a,4,8a-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H28O5/c1-10-4-7-15(20)13(3,18)6-5-11(8-14(10,15)19)12(2,17)9-16/h10-11,16-20H,4-9H2,1-3H3/t10-,11+,12?,13+,14+,15+/m0/s1
InChI Key VSZFUFYQDUYMSE-CXHAHFFASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O5
Molecular Weight 288.38 g/mol
Exact Mass 288.19367399 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP -0.50
Atomic LogP (AlogP) 0.17
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4S,5R,7R,10R)-guaiane-1,5,10,11,12-pentaol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8963 89.63%
Caco-2 + 0.5505 55.05%
Blood Brain Barrier + 0.5885 58.85%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.5193 51.93%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9329 93.29%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8150 81.50%
BSEP inhibitior - 0.8183 81.83%
P-glycoprotein inhibitior - 0.9404 94.04%
P-glycoprotein substrate - 0.7292 72.92%
CYP3A4 substrate + 0.6082 60.82%
CYP2C9 substrate - 0.6061 60.61%
CYP2D6 substrate - 0.7518 75.18%
CYP3A4 inhibition - 0.8954 89.54%
CYP2C9 inhibition - 0.7621 76.21%
CYP2C19 inhibition - 0.8148 81.48%
CYP2D6 inhibition - 0.9558 95.58%
CYP1A2 inhibition - 0.6965 69.65%
CYP2C8 inhibition - 0.7931 79.31%
CYP inhibitory promiscuity - 0.9782 97.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7451 74.51%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.6620 66.20%
Skin irritation - 0.5840 58.40%
Skin corrosion - 0.9547 95.47%
Ames mutagenesis - 0.8437 84.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5805 58.05%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5287 52.87%
skin sensitisation - 0.8501 85.01%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6266 62.66%
Acute Oral Toxicity (c) III 0.6041 60.41%
Estrogen receptor binding + 0.6191 61.91%
Androgen receptor binding - 0.4932 49.32%
Thyroid receptor binding + 0.5398 53.98%
Glucocorticoid receptor binding + 0.5423 54.23%
Aromatase binding + 0.6457 64.57%
PPAR gamma - 0.8183 81.83%
Honey bee toxicity - 0.8871 88.71%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.7010 70.10%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.78% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.38% 96.09%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 92.77% 100.00%
CHEMBL206 P03372 Estrogen receptor alpha 92.17% 97.64%
CHEMBL2996 Q05655 Protein kinase C delta 91.30% 97.79%
CHEMBL1871 P10275 Androgen Receptor 91.22% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.45% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 86.38% 95.93%
CHEMBL259 P32245 Melanocortin receptor 4 86.04% 95.38%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.99% 91.03%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.38% 96.61%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.08% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 84.18% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.98% 97.09%
CHEMBL234 P35462 Dopamine D3 receptor 82.13% 90.48%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.00% 95.50%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.52% 98.46%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 81.48% 95.27%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.34% 92.86%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.13% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 139585440
LOTUS LTS0124986
wikiData Q77422564