cis-Vitispirane

Details

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Internal ID cd912999-48a0-4367-a31b-e9af8bccfbc7
Taxonomy Organoheterocyclic compounds > Oxolanes
IUPAC Name (2S,5R)-2,6,6-trimethyl-10-methylidene-1-oxaspiro[4.5]dec-8-ene
SMILES (Canonical) CC1CCC2(O1)C(=C)C=CCC2(C)C
SMILES (Isomeric) C[C@H]1CC[C@]2(O1)C(=C)C=CCC2(C)C
InChI InChI=1S/C13H20O/c1-10-6-5-8-12(3,4)13(10)9-7-11(2)14-13/h5-6,11H,1,7-9H2,2-4H3/t11-,13-/m0/s1
InChI Key DUPDJVDPPBFBPL-AAEUAGOBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O
Molecular Weight 192.30 g/mol
Exact Mass 192.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.47
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Vitispirane B
Vitispirane II
Vitispirane, cis-
260K6CUA1F
DUPDJVDPPBFBPL-AAEUAGOBSA-N
Q27254018
(5R)-2beta,10,10-Trimethyl-6-methylene-1-oxaspiro[4.5]deca-7-ene
1-Oxaspiro(4.5)dec-7-ene, 2,10,10-trimethyl-6-methylene-, (2R,5S)-rel-

2D Structure

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2D Structure of cis-Vitispirane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.8861 88.61%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4829 48.29%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9050 90.50%
OATP1B3 inhibitior + 0.8722 87.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9444 94.44%
P-glycoprotein inhibitior - 0.9706 97.06%
P-glycoprotein substrate - 0.8928 89.28%
CYP3A4 substrate + 0.5278 52.78%
CYP2C9 substrate + 0.6043 60.43%
CYP2D6 substrate - 0.7856 78.56%
CYP3A4 inhibition - 0.8499 84.99%
CYP2C9 inhibition - 0.6727 67.27%
CYP2C19 inhibition + 0.5965 59.65%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.5060 50.60%
CYP2C8 inhibition - 0.8798 87.98%
CYP inhibitory promiscuity - 0.7402 74.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4966 49.66%
Eye corrosion - 0.9159 91.59%
Eye irritation - 0.6689 66.89%
Skin irritation + 0.5405 54.05%
Skin corrosion - 0.9696 96.96%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5398 53.98%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6481 64.81%
skin sensitisation + 0.7653 76.53%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6464 64.64%
Acute Oral Toxicity (c) III 0.8444 84.44%
Estrogen receptor binding - 0.9079 90.79%
Androgen receptor binding - 0.6041 60.41%
Thyroid receptor binding - 0.7553 75.53%
Glucocorticoid receptor binding - 0.8277 82.77%
Aromatase binding - 0.8690 86.90%
PPAR gamma - 0.8533 85.33%
Honey bee toxicity - 0.8431 84.31%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9722 97.22%

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 91.31% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.57% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.91% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.71% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.07% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.58% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.46% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.35% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.38% 94.80%

Cross-Links

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PubChem 91748031
NPASS NPC307064
LOTUS LTS0220628
wikiData Q27254018