1,6-Germacradien-5-ol

Details

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Internal ID 322344cf-0a0b-478c-b4cd-ada13232cf9e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (2Z,7Z)-3,7-dimethyl-10-propan-2-ylcyclodeca-2,7-dien-1-ol
SMILES (Canonical) CC1=CCC(C(C=C(CCC1)C)O)C(C)C
SMILES (Isomeric) C/C/1=C/CC(C(/C=C(\CCC1)/C)O)C(C)C
InChI InChI=1S/C15H26O/c1-11(2)14-9-8-12(3)6-5-7-13(4)10-15(14)16/h8,10-11,14-16H,5-7,9H2,1-4H3/b12-8-,13-10-
InChI Key JZGKKDAVPHTIQS-KDVDBFTISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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JZGKKDAVPHTIQS-KDVDBFTISA-N

2D Structure

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2D Structure of 1,6-Germacradien-5-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.9474 94.74%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4740 47.40%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9466 94.66%
OATP1B3 inhibitior + 0.9318 93.18%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8765 87.65%
P-glycoprotein inhibitior - 0.9274 92.74%
P-glycoprotein substrate - 0.9314 93.14%
CYP3A4 substrate - 0.6004 60.04%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.8096 80.96%
CYP2C9 inhibition - 0.7546 75.46%
CYP2C19 inhibition - 0.7735 77.35%
CYP2D6 inhibition - 0.9104 91.04%
CYP1A2 inhibition - 0.5741 57.41%
CYP2C8 inhibition - 0.9635 96.35%
CYP inhibitory promiscuity - 0.7251 72.51%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.6152 61.52%
Eye corrosion - 0.8378 83.78%
Eye irritation - 0.7177 71.77%
Skin irritation + 0.6941 69.41%
Skin corrosion - 0.8583 85.83%
Ames mutagenesis - 0.7982 79.82%
Human Ether-a-go-go-Related Gene inhibition + 0.6458 64.58%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.8266 82.66%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6164 61.64%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.7013 70.13%
Acute Oral Toxicity (c) III 0.5709 57.09%
Estrogen receptor binding - 0.9253 92.53%
Androgen receptor binding - 0.8097 80.97%
Thyroid receptor binding - 0.6485 64.85%
Glucocorticoid receptor binding - 0.7892 78.92%
Aromatase binding - 0.9019 90.19%
PPAR gamma - 0.7409 74.09%
Honey bee toxicity - 0.9331 93.31%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9864 98.64%

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
CHEMBL2581 P07339 Cathepsin D 91.45% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.45% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.70% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.73% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.95% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.78% 93.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.16% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.08% 97.09%

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.
Elsholtzia ciliata
Mosla chinensis

Cross-Links

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PubChem 91748908
NPASS NPC10315