beta-Necrodol

Details

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Internal ID d50b75a1-8720-4d92-8703-458c4d4f3c70
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name [(1R,3R)-2,2,3-trimethyl-4-methylidenecyclopentyl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O/c1-7-5-9(6-11)10(3,4)8(7)2/h8-9,11H,1,5-6H2,2-4H3/t8-,9+/m1/s1
InChI Key QPEVOWJNFFZVOF-BDAKNGLRSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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104086-70-6
[(1R,3R)-2,2,3-trimethyl-4-methylidenecyclopentyl]methanol

2D Structure

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2D Structure of beta-Necrodol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 - 0.5618 56.18%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.7596 75.96%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.9171 91.71%
OATP1B3 inhibitior + 0.8757 87.57%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9540 95.40%
P-glycoprotein inhibitior - 0.9744 97.44%
P-glycoprotein substrate - 0.8831 88.31%
CYP3A4 substrate - 0.6139 61.39%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.7754 77.54%
CYP3A4 inhibition - 0.7747 77.47%
CYP2C9 inhibition - 0.8378 83.78%
CYP2C19 inhibition - 0.7871 78.71%
CYP2D6 inhibition - 0.9272 92.72%
CYP1A2 inhibition - 0.8423 84.23%
CYP2C8 inhibition - 0.9614 96.14%
CYP inhibitory promiscuity - 0.6996 69.96%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6428 64.28%
Carcinogenicity (trinary) Non-required 0.6265 62.65%
Eye corrosion - 0.7492 74.92%
Eye irritation + 0.9292 92.92%
Skin irritation + 0.6109 61.09%
Skin corrosion - 0.7229 72.29%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6709 67.09%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5177 51.77%
skin sensitisation + 0.6262 62.62%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6505 65.05%
Acute Oral Toxicity (c) III 0.7955 79.55%
Estrogen receptor binding - 0.8227 82.27%
Androgen receptor binding - 0.7334 73.34%
Thyroid receptor binding - 0.7766 77.66%
Glucocorticoid receptor binding - 0.7237 72.37%
Aromatase binding - 0.7001 70.01%
PPAR gamma - 0.7819 78.19%
Honey bee toxicity - 0.9076 90.76%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9399 93.99%

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 93.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.17% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.25% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 85.83% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.72% 97.09%
CHEMBL2581 P07339 Cathepsin D 85.09% 98.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.77% 95.50%

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.
There are no matching plants.

Cross-Links

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PubChem 10920731
LOTUS LTS0234228
wikiData Q105225340