Dihydrolycopodine (5-OH)

Details

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Internal ID 0b508ddd-051f-461b-969a-ed8defa1ab0f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,10S,11R,13S,15R)-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadecan-11-ol
SMILES (Canonical) CC1CC2CC(C3CCCN4C3(C1)C2CCC4)O
SMILES (Isomeric) C[C@@H]1C[C@H]2C[C@H]([C@H]3CCCN4[C@]3(C1)[C@@H]2CCC4)O
InChI InChI=1S/C16H27NO/c1-11-8-12-9-15(18)14-5-3-7-17-6-2-4-13(12)16(14,17)10-11/h11-15,18H,2-10H2,1H3/t11-,12+,13-,14-,15-,16-/m1/s1
InChI Key ICWQJNDZXVMLCK-JXEZDRHFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H27NO
Molecular Weight 249.39 g/mol
Exact Mass 249.209264485 g/mol
Topological Polar Surface Area (TPSA) 23.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dihydrolycopodine (5-OH)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 + 0.7113 71.13%
Blood Brain Barrier + 0.9629 96.29%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.6567 65.67%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9516 95.16%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.8397 83.97%
P-glycoprotein inhibitior - 0.9323 93.23%
P-glycoprotein substrate - 0.7973 79.73%
CYP3A4 substrate + 0.5353 53.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5975 59.75%
CYP3A4 inhibition - 0.7991 79.91%
CYP2C9 inhibition - 0.8865 88.65%
CYP2C19 inhibition - 0.9265 92.65%
CYP2D6 inhibition + 0.5521 55.21%
CYP1A2 inhibition - 0.9383 93.83%
CYP2C8 inhibition - 0.9179 91.79%
CYP inhibitory promiscuity - 0.9862 98.62%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5697 56.97%
Eye corrosion - 0.9650 96.50%
Eye irritation + 0.6263 62.63%
Skin irritation - 0.5588 55.88%
Skin corrosion - 0.5000 50.00%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6114 61.14%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5657 56.57%
skin sensitisation - 0.8133 81.33%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.7139 71.39%
Acute Oral Toxicity (c) III 0.6511 65.11%
Estrogen receptor binding - 0.6358 63.58%
Androgen receptor binding - 0.4815 48.15%
Thyroid receptor binding + 0.5257 52.57%
Glucocorticoid receptor binding - 0.6218 62.18%
Aromatase binding - 0.6535 65.35%
PPAR gamma - 0.8236 82.36%
Honey bee toxicity - 0.8960 89.60%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.9223 92.23%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.04% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.04% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.77% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 92.39% 95.58%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 91.94% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.40% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.63% 92.94%
CHEMBL206 P03372 Estrogen receptor alpha 85.28% 97.64%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.76% 94.78%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.09% 90.24%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.85% 98.99%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.82% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.52% 95.50%
CHEMBL226 P30542 Adenosine A1 receptor 82.47% 95.93%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 82.02% 96.03%
CHEMBL237 P41145 Kappa opioid receptor 81.72% 98.10%
CHEMBL238 Q01959 Dopamine transporter 81.64% 95.88%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.60% 99.18%
CHEMBL1871 P10275 Androgen Receptor 80.83% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.34% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.21% 91.03%

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.
Lycopodium carolinum
Lycopodium lagopus
Lycopodium volubile

Cross-Links

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PubChem 21581107
LOTUS LTS0067903
wikiData Q105111206