Anastreptene

Details

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Internal ID cdd5fa7c-d918-42e9-aae7-90f8c938591f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Aromadendrane sesquiterpenoids > 5,10-cycloaromadendrane sesquiterpenoids
IUPAC Name (1R,2S,4R)-3,3,7,11-tetramethyltetracyclo[5.4.0.01,8.02,4]undec-10-ene
SMILES (Canonical) CC1=CCC2C13C2(CCC4C3C4(C)C)C
SMILES (Isomeric) CC1=CCC2[C@]13C2(CC[C@@H]4[C@H]3C4(C)C)C
InChI InChI=1S/C15H22/c1-9-5-6-11-14(4)8-7-10-12(13(10,2)3)15(9,11)14/h5,10-12H,6-8H2,1-4H3/t10-,11?,12+,14?,15-/m1/s1
InChI Key SYNYVXGDEQOMCB-OGNMTSBISA-N
Popularity 17 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 4.10
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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SYNYVXGDEQOMCB-OGNMTSBISA-N
Q67879688

2D Structure

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2D Structure of Anastreptene

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 + 0.6899 68.99%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.6788 67.88%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.9107 91.07%
OATP1B3 inhibitior + 0.9307 93.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9419 94.19%
P-glycoprotein inhibitior - 0.9319 93.19%
P-glycoprotein substrate - 0.9333 93.33%
CYP3A4 substrate + 0.5463 54.63%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7431 74.31%
CYP3A4 inhibition - 0.8741 87.41%
CYP2C9 inhibition - 0.6884 68.84%
CYP2C19 inhibition - 0.5848 58.48%
CYP2D6 inhibition - 0.9144 91.44%
CYP1A2 inhibition - 0.7676 76.76%
CYP2C8 inhibition - 0.7096 70.96%
CYP inhibitory promiscuity - 0.5431 54.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4894 48.94%
Eye corrosion - 0.9588 95.88%
Eye irritation - 0.5617 56.17%
Skin irritation - 0.5463 54.63%
Skin corrosion - 0.9529 95.29%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4947 49.47%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5274 52.74%
skin sensitisation + 0.7757 77.57%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.4566 45.66%
Acute Oral Toxicity (c) III 0.7948 79.48%
Estrogen receptor binding - 0.7721 77.21%
Androgen receptor binding + 0.6508 65.08%
Thyroid receptor binding - 0.7033 70.33%
Glucocorticoid receptor binding - 0.8210 82.10%
Aromatase binding - 0.7154 71.54%
PPAR gamma - 0.7229 72.29%
Honey bee toxicity - 0.7718 77.18%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL1871 P10275 Androgen Receptor 89.08% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.08% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 88.76% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.28% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.69% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.45% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.21% 82.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.01% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.34% 86.00%

Cross-Links

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PubChem 91746864
LOTUS LTS0033607
wikiData Q67879688