(-)-Obtusadiene

Details

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Internal ID f322c28b-85bf-497d-afa9-ae2cd325c969
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Chamigranes
IUPAC Name (3S,4R,6R)-4-bromo-5,5,9-trimethyl-1-methylidenespiro[5.5]undeca-8,10-dien-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H21BrO/c1-10-5-7-15(8-6-10)11(2)9-12(17)13(16)14(15,3)4/h5-7,12-13,17H,2,8-9H2,1,3-4H3/t12-,13-,15-/m0/s1
InChI Key ITZMWVKTANMHQA-YDHLFZDLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H21BrO
Molecular Weight 297.23 g/mol
Exact Mass 296.07758 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.99
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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(-)-10beta-bormo-1,3,7(14)-chamigratrien-9alpha-ol
(3S,4R,6R)-4-bromo-5,5,9-trimethyl-1-methylidenespiro[5.5]undeca-8,10-dien-3-ol
(3S,4R,6R)-4-bromo-5,5,9-trimethyl-1-methylidenespiro(5.5)undeca-8,10-dien-3-ol
RefChem:67915
CHEBI:137716
LMPR0103670001

2D Structure

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2D Structure of (-)-Obtusadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.8673 86.73%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5798 57.98%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9354 93.54%
OATP1B3 inhibitior + 0.9103 91.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7635 76.35%
P-glycoprotein inhibitior - 0.9654 96.54%
P-glycoprotein substrate - 0.7865 78.65%
CYP3A4 substrate + 0.5491 54.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7789 77.89%
CYP3A4 inhibition - 0.6204 62.04%
CYP2C9 inhibition - 0.6083 60.83%
CYP2C19 inhibition - 0.6181 61.81%
CYP2D6 inhibition - 0.9203 92.03%
CYP1A2 inhibition - 0.8326 83.26%
CYP2C8 inhibition - 0.8935 89.35%
CYP inhibitory promiscuity - 0.7071 70.71%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.5658 56.58%
Eye corrosion - 0.9668 96.68%
Eye irritation - 0.8424 84.24%
Skin irritation + 0.5104 51.04%
Skin corrosion - 0.9088 90.88%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3798 37.98%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.5925 59.25%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4945 49.45%
Acute Oral Toxicity (c) III 0.7077 70.77%
Estrogen receptor binding - 0.8912 89.12%
Androgen receptor binding - 0.6567 65.67%
Thyroid receptor binding - 0.6872 68.72%
Glucocorticoid receptor binding - 0.7071 70.71%
Aromatase binding - 0.6862 68.62%
PPAR gamma - 0.6435 64.35%
Honey bee toxicity - 0.9301 93.01%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9937 99.37%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.24% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 91.47% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.44% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 83.67% 90.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.64% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.74% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.29% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.15% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.81% 94.45%

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 15599842
LOTUS LTS0059038
wikiData Q76506759