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

Details

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Internal ID 9e2c5315-4e6b-4618-9e17-994528fb9a31
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (1R,3S,3aS,4R,7R,8aR)-7-(1,2-dihydroxypropan-2-yl)-1,4-dimethyl-2,3,3a,5,6,7,8,8a-octahydroazulene-1,3,4-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H28O5/c1-13(18)5-4-9(15(3,20)8-16)6-10-12(13)11(17)7-14(10,2)19/h9-12,16-20H,4-8H2,1-3H3/t9-,10-,11+,12+,13-,14-,15?/m1/s1
InChI Key IXFRQVRAVLEFDG-KYHUKMSWSA-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 -0.60
Atomic LogP (AlogP) 0.03
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 (1S,2S,4R,5R,7R,10R)-guaiane-2,4,10,11,12-pentaol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9109 91.09%
Caco-2 - 0.5774 57.74%
Blood Brain Barrier + 0.5635 56.35%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.5783 57.83%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8150 81.50%
BSEP inhibitior - 0.8134 81.34%
P-glycoprotein inhibitior - 0.9275 92.75%
P-glycoprotein substrate - 0.7352 73.52%
CYP3A4 substrate + 0.6233 62.33%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.7387 73.87%
CYP3A4 inhibition - 0.9034 90.34%
CYP2C9 inhibition - 0.7438 74.38%
CYP2C19 inhibition - 0.8002 80.02%
CYP2D6 inhibition - 0.9495 94.95%
CYP1A2 inhibition - 0.6806 68.06%
CYP2C8 inhibition - 0.6618 66.18%
CYP inhibitory promiscuity - 0.9786 97.86%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7462 74.62%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.7829 78.29%
Skin irritation - 0.6335 63.35%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.7637 76.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5856 58.56%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5226 52.26%
skin sensitisation - 0.8325 83.25%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5074 50.74%
Acute Oral Toxicity (c) III 0.6509 65.09%
Estrogen receptor binding + 0.7044 70.44%
Androgen receptor binding - 0.5953 59.53%
Thyroid receptor binding + 0.6457 64.57%
Glucocorticoid receptor binding + 0.7193 71.93%
Aromatase binding + 0.6812 68.12%
PPAR gamma - 0.8186 81.86%
Honey bee toxicity - 0.7953 79.53%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.4292 42.92%

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 99.68% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 97.39% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.15% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 96.21% 97.79%
CHEMBL218 P21554 Cannabinoid CB1 receptor 95.21% 96.61%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 95.11% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.92% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.62% 100.00%
CHEMBL1871 P10275 Androgen Receptor 89.57% 96.43%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.18% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.48% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.12% 91.11%
CHEMBL237 P41145 Kappa opioid receptor 87.90% 98.10%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 84.49% 87.16%
CHEMBL206 P03372 Estrogen receptor alpha 83.99% 97.64%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.92% 91.03%
CHEMBL1937 Q92769 Histone deacetylase 2 83.87% 94.75%
CHEMBL259 P32245 Melanocortin receptor 4 83.40% 95.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.04% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.60% 95.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.04% 92.94%
CHEMBL221 P23219 Cyclooxygenase-1 81.84% 90.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.74% 97.14%
CHEMBL2581 P07339 Cathepsin D 81.12% 98.95%
CHEMBL220 P22303 Acetylcholinesterase 80.67% 94.45%

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 139588104
LOTUS LTS0062971
wikiData Q105122124