9-(3-Hydroxyprop-1-en-2-yl)-2,6-dimethylidenecyclodecane-1,5-diol

Details

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Internal ID 459e9590-0cb9-44ec-8139-070faa26ec59
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 9-(3-hydroxyprop-1-en-2-yl)-2,6-dimethylidenecyclodecane-1,5-diol
SMILES (Canonical) C=C1CCC(CC(C(=C)CCC1O)O)C(=C)CO
SMILES (Isomeric) C=C1CCC(CC(C(=C)CCC1O)O)C(=C)CO
InChI InChI=1S/C15H24O3/c1-10-4-6-13(12(3)9-16)8-15(18)11(2)5-7-14(10)17/h13-18H,1-9H2
InChI Key VYJPSNRDHOGIPH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-(3-Hydroxyprop-1-en-2-yl)-2,6-dimethylidenecyclodecane-1,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9821 98.21%
Caco-2 - 0.7370 73.70%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7609 76.09%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9465 94.65%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6542 65.42%
BSEP inhibitior - 0.9281 92.81%
P-glycoprotein inhibitior - 0.9288 92.88%
P-glycoprotein substrate - 0.8940 89.40%
CYP3A4 substrate - 0.5610 56.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7035 70.35%
CYP3A4 inhibition - 0.7760 77.60%
CYP2C9 inhibition - 0.8502 85.02%
CYP2C19 inhibition - 0.7584 75.84%
CYP2D6 inhibition - 0.8672 86.72%
CYP1A2 inhibition - 0.7916 79.16%
CYP2C8 inhibition - 0.8406 84.06%
CYP inhibitory promiscuity - 0.8292 82.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.7043 70.43%
Eye corrosion - 0.9143 91.43%
Eye irritation + 0.9271 92.71%
Skin irritation - 0.7563 75.63%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5918 59.18%
Micronuclear - 0.8841 88.41%
Hepatotoxicity - 0.5073 50.73%
skin sensitisation - 0.5498 54.98%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4538 45.38%
Acute Oral Toxicity (c) III 0.7445 74.45%
Estrogen receptor binding - 0.5925 59.25%
Androgen receptor binding - 0.6490 64.90%
Thyroid receptor binding - 0.5970 59.70%
Glucocorticoid receptor binding + 0.6886 68.86%
Aromatase binding - 0.7149 71.49%
PPAR gamma - 0.7314 73.14%
Honey bee toxicity - 0.9275 92.75%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7057 70.57%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.45% 83.82%
CHEMBL226 P30542 Adenosine A1 receptor 92.33% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.97% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.45% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.05% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.04% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.03% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.02% 96.09%

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.
Artemisia reptans
Seriphidium herba-alba

Cross-Links

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PubChem 14705670
LOTUS LTS0120528
wikiData Q105299034