African-5-ene

Details

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Internal ID 64c7fdfa-8f0f-4f7a-a403-bb286f6c0339
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name (1aR,7bR)-3,3,5,7b-tetramethyl-1a,2,5,6,7,7a-hexahydro-1H-cyclopropa[e]azulene
SMILES (Canonical) CC1CCC2C1=CC(CC3C2(C3)C)(C)C
SMILES (Isomeric) CC1CCC2C1=CC(C[C@@H]3[C@]2(C3)C)(C)C
InChI InChI=1S/C15H24/c1-10-5-6-13-12(10)9-14(2,3)7-11-8-15(11,13)4/h9-11,13H,5-8H2,1-4H3/t10?,11-,13?,15+/m0/s1
InChI Key FCQGZOYPTSMOOM-OGOZRWHJSA-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) 4.42
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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FCQGZOYPTSMOOM-OGOZRWHJSA-N

2D Structure

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2D Structure of African-5-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.8731 87.31%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.6807 68.07%
OATP2B1 inhibitior - 0.8448 84.48%
OATP1B1 inhibitior + 0.9019 90.19%
OATP1B3 inhibitior + 0.9657 96.57%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9354 93.54%
P-glycoprotein inhibitior - 0.9504 95.04%
P-glycoprotein substrate - 0.8050 80.50%
CYP3A4 substrate + 0.5220 52.20%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.9372 93.72%
CYP2C9 inhibition - 0.6680 66.80%
CYP2C19 inhibition - 0.6605 66.05%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition - 0.6697 66.97%
CYP2C8 inhibition - 0.9511 95.11%
CYP inhibitory promiscuity - 0.7471 74.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4776 47.76%
Eye corrosion - 0.9219 92.19%
Eye irritation + 0.6626 66.26%
Skin irritation + 0.5798 57.98%
Skin corrosion - 0.9643 96.43%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6945 69.45%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.7724 77.24%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5998 59.98%
Acute Oral Toxicity (c) III 0.8165 81.65%
Estrogen receptor binding - 0.7080 70.80%
Androgen receptor binding - 0.7293 72.93%
Thyroid receptor binding - 0.6170 61.70%
Glucocorticoid receptor binding - 0.6840 68.40%
Aromatase binding - 0.6637 66.37%
PPAR gamma - 0.7840 78.40%
Honey bee toxicity - 0.9149 91.49%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9956 99.56%

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 91.95% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.73% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.50% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.71% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.54% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.51% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.31% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.23% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.56% 95.89%
CHEMBL4444 P04070 Vitamin K-dependent protein C 81.24% 93.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.94% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.44% 92.94%

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.
Arnebia euchroma
Arnebia guttata
Lithospermum erythrorhizon

Cross-Links

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PubChem 91750055
NPASS NPC225582