(2Z,3R,4S,5R)-2-but-2-ynylidene-6-oxaspiro[4.5]decane-3,4-diol

Details

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Internal ID 5a38b7ec-cca2-4140-a7a2-03a54fc0157a
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name (2Z,3R,4S,5R)-2-but-2-ynylidene-6-oxaspiro[4.5]decane-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O3/c1-2-3-6-10-9-13(12(15)11(10)14)7-4-5-8-16-13/h6,11-12,14-15H,4-5,7-9H2,1H3/b10-6-/t11-,12+,13-/m1/s1
InChI Key RZEXIMRXKVYRLP-YRHGKNAFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O3
Molecular Weight 222.28 g/mol
Exact Mass 222.125594432 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.00
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2Z,3R,4S,5R)-2-but-2-ynylidene-6-oxaspiro[4.5]decane-3,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8920 89.20%
Caco-2 - 0.6614 66.14%
Blood Brain Barrier - 0.5322 53.22%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7893 78.93%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8818 88.18%
OATP1B3 inhibitior + 0.9710 97.10%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7069 70.69%
BSEP inhibitior - 0.8450 84.50%
P-glycoprotein inhibitior - 0.9571 95.71%
P-glycoprotein substrate - 0.8806 88.06%
CYP3A4 substrate + 0.5183 51.83%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7880 78.80%
CYP3A4 inhibition - 0.9599 95.99%
CYP2C9 inhibition - 0.8411 84.11%
CYP2C19 inhibition - 0.7022 70.22%
CYP2D6 inhibition - 0.9156 91.56%
CYP1A2 inhibition - 0.7580 75.80%
CYP2C8 inhibition - 0.9039 90.39%
CYP inhibitory promiscuity - 0.9155 91.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5282 52.82%
Eye corrosion - 0.9678 96.78%
Eye irritation - 0.9457 94.57%
Skin irritation - 0.7190 71.90%
Skin corrosion - 0.9299 92.99%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6641 66.41%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.7540 75.40%
skin sensitisation - 0.7964 79.64%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6121 61.21%
Acute Oral Toxicity (c) III 0.4918 49.18%
Estrogen receptor binding - 0.6963 69.63%
Androgen receptor binding - 0.7208 72.08%
Thyroid receptor binding - 0.5370 53.70%
Glucocorticoid receptor binding - 0.5075 50.75%
Aromatase binding - 0.7514 75.14%
PPAR gamma - 0.7309 73.09%
Honey bee toxicity - 0.8589 85.89%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.4095 40.95%

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 94.89% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.28% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.40% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.74% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.23% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 80.93% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.55% 95.56%

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.
Matricaria aurea

Cross-Links

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PubChem 162926559
LOTUS LTS0090506
wikiData Q105248348