Herbertene

Details

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Internal ID 50eea38e-e469-4712-a57f-02c631e65ed3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-3-[(1S)-1,2,2-trimethylcyclopentyl]benzene
SMILES (Canonical) CC1=CC(=CC=C1)C2(CCCC2(C)C)C
SMILES (Isomeric) CC1=CC(=CC=C1)[C@]2(CCCC2(C)C)C
InChI InChI=1S/C15H22/c1-12-7-5-8-13(11-12)15(4)10-6-9-14(15,2)3/h5,7-8,11H,6,9-10H2,1-4H3/t15-/m1/s1
InChI Key BBZBREYBGRYINI-OAHLLOKOSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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BBZBREYBGRYINI-OAHLLOKOSA-N
1-methyl-3-[(1S)-1,2,2-trimethylcyclopentyl]benzene
80322-46-9

2D Structure

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2D Structure of Herbertene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.9713 97.13%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5018 50.18%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9543 95.43%
OATP1B3 inhibitior + 0.9261 92.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6270 62.70%
P-glycoprotein inhibitior - 0.9786 97.86%
P-glycoprotein substrate - 0.9076 90.76%
CYP3A4 substrate - 0.5650 56.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6793 67.93%
CYP3A4 inhibition - 0.9113 91.13%
CYP2C9 inhibition - 0.8942 89.42%
CYP2C19 inhibition - 0.9131 91.31%
CYP2D6 inhibition - 0.9517 95.17%
CYP1A2 inhibition - 0.8370 83.70%
CYP2C8 inhibition - 0.9375 93.75%
CYP inhibitory promiscuity - 0.7086 70.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4532 45.32%
Eye corrosion - 0.7644 76.44%
Eye irritation + 0.6766 67.66%
Skin irritation + 0.5221 52.21%
Skin corrosion - 0.9830 98.30%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4442 44.42%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6728 67.28%
skin sensitisation + 0.7802 78.02%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5151 51.51%
Mitochondrial toxicity - 0.6090 60.90%
Nephrotoxicity - 0.7652 76.52%
Acute Oral Toxicity (c) III 0.5863 58.63%
Estrogen receptor binding - 0.8165 81.65%
Androgen receptor binding - 0.5247 52.47%
Thyroid receptor binding - 0.6769 67.69%
Glucocorticoid receptor binding - 0.8500 85.00%
Aromatase binding - 0.7867 78.67%
PPAR gamma - 0.8148 81.48%
Honey bee toxicity - 0.9702 97.02%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9967 99.67%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.27% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.36% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.46% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 88.59% 96.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.09% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 85.20% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.01% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.74% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.16% 94.62%
CHEMBL240 Q12809 HERG 81.64% 89.76%
CHEMBL3568 P29475 Nitric-oxide synthase, brain 80.64% 95.46%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.33% 96.25%

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.
Cinnamomum philippinense
Herbertus aduncus
Herbertus dicranus
Herbertus sakuraii
Mastigophora diclados
Metacalypogeia alternifolia

Cross-Links

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PubChem 10910593
NPASS NPC150039
LOTUS LTS0238880
wikiData Q104254423