(4S,5S)-Germacrone-4,5-epoxide

Details

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Internal ID 582740a9-cb71-4d45-a940-68a2055847c4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (1S,10R)-6,10-dimethyl-3-propan-2-ylidene-11-oxabicyclo[8.1.0]undec-6-en-4-one
SMILES (Canonical) CC1=CCCC2(C(O2)CC(=C(C)C)C(=O)C1)C
SMILES (Isomeric) CC1=CCC[C@@]2([C@@H](O2)CC(=C(C)C)C(=O)C1)C
InChI InChI=1S/C15H22O2/c1-10(2)12-9-14-15(4,17-14)7-5-6-11(3)8-13(12)16/h6,14H,5,7-9H2,1-4H3/t14-,15+/m0/s1
InChI Key DWGVRYKQVZGSIB-LSDHHAIUSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 29.60 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.57
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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(4S,5S)-Germacrone-4,5-epoxide

2D Structure

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2D Structure of (4S,5S)-Germacrone-4,5-epoxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8464 84.64%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5236 52.36%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9507 95.07%
OATP1B3 inhibitior + 0.9652 96.52%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.6924 69.24%
P-glycoprotein inhibitior - 0.9233 92.33%
P-glycoprotein substrate - 0.9103 91.03%
CYP3A4 substrate + 0.5653 56.53%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8544 85.44%
CYP3A4 inhibition - 0.7800 78.00%
CYP2C9 inhibition - 0.7294 72.94%
CYP2C19 inhibition + 0.5284 52.84%
CYP2D6 inhibition - 0.9418 94.18%
CYP1A2 inhibition + 0.7087 70.87%
CYP2C8 inhibition - 0.8211 82.11%
CYP inhibitory promiscuity - 0.9051 90.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5623 56.23%
Eye corrosion - 0.9608 96.08%
Eye irritation + 0.7084 70.84%
Skin irritation + 0.5730 57.30%
Skin corrosion - 0.9564 95.64%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4598 45.98%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5805 58.05%
skin sensitisation + 0.7362 73.62%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6373 63.73%
Acute Oral Toxicity (c) III 0.7023 70.23%
Estrogen receptor binding - 0.7565 75.65%
Androgen receptor binding - 0.7204 72.04%
Thyroid receptor binding - 0.7161 71.61%
Glucocorticoid receptor binding - 0.6471 64.71%
Aromatase binding - 0.8717 87.17%
PPAR gamma - 0.6918 69.18%
Honey bee toxicity - 0.8733 87.33%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9397 93.97%

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 95.80% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.80% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.79% 85.14%
CHEMBL2581 P07339 Cathepsin D 91.10% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.23% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.04% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.31% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.16% 99.23%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.90% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.08% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.41% 96.61%
CHEMBL4208 P20618 Proteasome component C5 83.62% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 82.88% 94.73%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.28% 96.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.65% 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.
Curcuma kwangsiensis
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria

Cross-Links

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PubChem 91753231
NPASS NPC12463