1(10)E,5E-germacradiene-9beta,11-diol

Details

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Internal ID 827a386b-97cf-44c8-9515-521bbe695840
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (1S,2E,6S,7E,9R)-9-(2-hydroxypropan-2-yl)-2,6-dimethylcyclodeca-2,7-dien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O2/c1-11-6-5-7-12(2)14(16)10-13(9-8-11)15(3,4)17/h7-9,11,13-14,16-17H,5-6,10H2,1-4H3/b9-8+,12-7+/t11-,13-,14-/m0/s1
InChI Key DXVZUYIXOHXNBU-ALKIPFEHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1(10)E,5E-germacradiene-9beta,11-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.7183 71.83%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5100 51.00%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9504 95.04%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7519 75.19%
P-glycoprotein inhibitior - 0.9401 94.01%
P-glycoprotein substrate - 0.6694 66.94%
CYP3A4 substrate - 0.5148 51.48%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7641 76.41%
CYP3A4 inhibition - 0.8500 85.00%
CYP2C9 inhibition - 0.8625 86.25%
CYP2C19 inhibition - 0.8019 80.19%
CYP2D6 inhibition - 0.9297 92.97%
CYP1A2 inhibition - 0.7401 74.01%
CYP2C8 inhibition - 0.7815 78.15%
CYP inhibitory promiscuity - 0.7960 79.60%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8028 80.28%
Carcinogenicity (trinary) Non-required 0.6033 60.33%
Eye corrosion - 0.9670 96.70%
Eye irritation - 0.9303 93.03%
Skin irritation + 0.6213 62.13%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4391 43.91%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.7478 74.78%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7097 70.97%
Acute Oral Toxicity (c) III 0.7911 79.11%
Estrogen receptor binding - 0.8492 84.92%
Androgen receptor binding - 0.8292 82.92%
Thyroid receptor binding + 0.5393 53.93%
Glucocorticoid receptor binding - 0.4826 48.26%
Aromatase binding - 0.8404 84.04%
PPAR gamma - 0.7108 71.08%
Honey bee toxicity - 0.9050 90.50%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.8628 86.28%

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 97.99% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.67% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.81% 92.94%
CHEMBL1871 P10275 Androgen Receptor 85.04% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.61% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.95% 97.21%
CHEMBL2581 P07339 Cathepsin D 83.86% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.45% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.85% 96.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.60% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.10% 89.00%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.05% 90.93%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139591588
LOTUS LTS0012905
wikiData Q104991224