Germazone

Details

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Internal ID 6104ed67-e731-43e1-9b9c-f204b804a799
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,7-dimethyl-4-propan-2-ylidenetricyclo[4.4.0.02,7]decan-3-one
SMILES (Canonical) CC(=C1CC2C3(CCCC2(C3C1=O)C)C)C
SMILES (Isomeric) CC(=C1CC2C3(CCCC2(C3C1=O)C)C)C
InChI InChI=1S/C15H22O/c1-9(2)10-8-11-14(3)6-5-7-15(11,4)13(14)12(10)16/h11,13H,5-8H2,1-4H3
InChI Key BBZWSYDKASNBSO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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62332-96-1
DTXSID60977885
BBZWSYDKASNBSO-UHFFFAOYSA-N
1,7-Dimethyl-4-(propan-2-ylidene)tricyclo[4.4.0.0~2,7~]decan-3-one
1,7-dimethyl-4-(propan-2-ylidene)tricyclo[4.4.0.02,7]decan-3-one
Tricyclo[4.4.0.02,7]decan-3-one, 1,7-dimethyl-4-(1-methylethylidene)-

2D Structure

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2D Structure of Germazone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8161 81.61%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5109 51.09%
OATP2B1 inhibitior - 0.8443 84.43%
OATP1B1 inhibitior + 0.8921 89.21%
OATP1B3 inhibitior + 0.8963 89.63%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8467 84.67%
P-glycoprotein inhibitior - 0.8961 89.61%
P-glycoprotein substrate - 0.9688 96.88%
CYP3A4 substrate + 0.5058 50.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8716 87.16%
CYP3A4 inhibition - 0.8543 85.43%
CYP2C9 inhibition - 0.7138 71.38%
CYP2C19 inhibition - 0.5098 50.98%
CYP2D6 inhibition - 0.9452 94.52%
CYP1A2 inhibition - 0.7499 74.99%
CYP2C8 inhibition - 0.9683 96.83%
CYP inhibitory promiscuity - 0.7005 70.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4718 47.18%
Eye corrosion - 0.9786 97.86%
Eye irritation + 0.8926 89.26%
Skin irritation + 0.5830 58.30%
Skin corrosion - 0.9723 97.23%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6117 61.17%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5574 55.74%
skin sensitisation + 0.8205 82.05%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.7041 70.41%
Acute Oral Toxicity (c) III 0.6701 67.01%
Estrogen receptor binding - 0.7347 73.47%
Androgen receptor binding - 0.5372 53.72%
Thyroid receptor binding - 0.5925 59.25%
Glucocorticoid receptor binding - 0.7154 71.54%
Aromatase binding - 0.7909 79.09%
PPAR gamma - 0.6718 67.18%
Honey bee toxicity - 0.9319 93.19%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9959 99.59%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.14% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.76% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.59% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.32% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.15% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.55% 99.23%

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.
Geranium macrorrhizum

Cross-Links

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PubChem 182335
LOTUS LTS0066484
wikiData Q82963193