(+)-Himachala-2,4-diene

Details

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Internal ID a106d065-9515-48e7-a7c9-8faa26177516
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Himachalane and lippifoliane sesquiterpenoids
IUPAC Name (9R,9aR)-3,5,5,9-tetramethyl-1,6,7,8,9,9a-hexahydrobenzo[7]annulene
SMILES (Canonical) CC1CCCC(C2=CC(=CCC12)C)(C)C
SMILES (Isomeric) C[C@@H]1CCCC(C2=CC(=CC[C@H]12)C)(C)C
InChI InChI=1S/C15H24/c1-11-7-8-13-12(2)6-5-9-15(3,4)14(13)10-11/h7,10,12-13H,5-6,8-9H2,1-4H3/t12-,13-/m1/s1
InChI Key JMGZKUMTFGHNRS-CHWSQXEVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-Himachala-2,4-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.8972 89.72%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7169 71.69%
OATP2B1 inhibitior - 0.8486 84.86%
OATP1B1 inhibitior + 0.8872 88.72%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8651 86.51%
P-glycoprotein inhibitior - 0.9572 95.72%
P-glycoprotein substrate - 0.9106 91.06%
CYP3A4 substrate + 0.5234 52.34%
CYP2C9 substrate - 0.8001 80.01%
CYP2D6 substrate - 0.7763 77.63%
CYP3A4 inhibition - 0.9106 91.06%
CYP2C9 inhibition - 0.7053 70.53%
CYP2C19 inhibition - 0.7164 71.64%
CYP2D6 inhibition - 0.9217 92.17%
CYP1A2 inhibition - 0.7916 79.16%
CYP2C8 inhibition - 0.7865 78.65%
CYP inhibitory promiscuity - 0.7783 77.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.4701 47.01%
Eye corrosion - 0.9150 91.50%
Eye irritation - 0.6008 60.08%
Skin irritation + 0.5844 58.44%
Skin corrosion - 0.9651 96.51%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6825 68.25%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5140 51.40%
skin sensitisation + 0.8306 83.06%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6712 67.12%
Acute Oral Toxicity (c) III 0.7611 76.11%
Estrogen receptor binding - 0.9506 95.06%
Androgen receptor binding - 0.5526 55.26%
Thyroid receptor binding - 0.6662 66.62%
Glucocorticoid receptor binding - 0.8270 82.70%
Aromatase binding - 0.8382 83.82%
PPAR gamma - 0.8866 88.66%
Honey bee toxicity - 0.9199 91.99%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9974 99.74%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.86% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.97% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 92.88% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.61% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.67% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.45% 94.80%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.09% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.71% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.89% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 82.83% 94.75%
CHEMBL1871 P10275 Androgen Receptor 82.61% 96.43%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 82.22% 90.71%

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.
Bazzania japonica
Capsicum annuum

Cross-Links

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PubChem 12993379
NPASS NPC68418
LOTUS LTS0272488
wikiData Q105131399