Gymnomitr-3-en-15-ol

Details

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Internal ID 5036570a-2394-4951-aff4-0002bc74f86a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (1,2,6-trimethyl-8-tricyclo[5.3.1.02,6]undec-8-enyl)methanol
SMILES (Canonical) CC12CCCC1(C3(CC=C(C2C3)CO)C)C
SMILES (Isomeric) CC12CCCC1(C3(CC=C(C2C3)CO)C)C
InChI InChI=1S/C15H24O/c1-13-8-5-11(10-16)12(9-13)14(2)6-4-7-15(13,14)3/h5,12,16H,4,6-10H2,1-3H3
InChI Key BOBUWMAINZVWRJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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BOBUWMAINZVWRJ-UHFFFAOYSA-N

2D Structure

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2D Structure of Gymnomitr-3-en-15-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.9396 93.96%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Lysosomes 0.8520 85.20%
OATP2B1 inhibitior - 0.8426 84.26%
OATP1B1 inhibitior + 0.8618 86.18%
OATP1B3 inhibitior + 0.8810 88.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7643 76.43%
P-glycoprotein inhibitior - 0.9525 95.25%
P-glycoprotein substrate - 0.8708 87.08%
CYP3A4 substrate - 0.5171 51.71%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7936 79.36%
CYP2C9 inhibition - 0.7255 72.55%
CYP2C19 inhibition - 0.7767 77.67%
CYP2D6 inhibition - 0.9060 90.60%
CYP1A2 inhibition - 0.7519 75.19%
CYP2C8 inhibition - 0.8813 88.13%
CYP inhibitory promiscuity - 0.6184 61.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6152 61.52%
Eye corrosion - 0.9614 96.14%
Eye irritation + 0.6180 61.80%
Skin irritation - 0.5829 58.29%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4658 46.58%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5743 57.43%
skin sensitisation + 0.5518 55.18%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8298 82.98%
Acute Oral Toxicity (c) III 0.8162 81.62%
Estrogen receptor binding - 0.8119 81.19%
Androgen receptor binding + 0.6110 61.10%
Thyroid receptor binding - 0.7413 74.13%
Glucocorticoid receptor binding - 0.8242 82.42%
Aromatase binding - 0.6547 65.47%
PPAR gamma - 0.8128 81.28%
Honey bee toxicity - 0.9323 93.23%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9883 98.83%

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 97.51% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.02% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.03% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.44% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 90.82% 97.79%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.77% 96.61%
CHEMBL226 P30542 Adenosine A1 receptor 88.27% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.09% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.12% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.89% 95.89%
CHEMBL2581 P07339 Cathepsin D 82.57% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.15% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.48% 95.56%
CHEMBL259 P32245 Melanocortin receptor 4 80.10% 95.38%

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.
Jungermannia infusca
Jungermannia truncata
Lejeunea aquatica

Cross-Links

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PubChem 91750191
LOTUS LTS0184517
wikiData Q104939146