Spiniferin-1

Details

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Internal ID c4da13eb-b263-4b33-be50-a8f01aca9046
Taxonomy Organoheterocyclic compounds > Cycloheptafurans
IUPAC Name 10,10-dimethyl-4-oxatricyclo[7.4.1.03,7]tetradeca-1,3(7),5,8,12-pentaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O/c1-15(2)6-3-4-11-8-13(15)10-12-5-7-16-14(12)9-11/h3-5,7,9-10H,6,8H2,1-2H3
InChI Key JKYQZVRIQNFMHF-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O
Molecular Weight 212.29 g/mol
Exact Mass 212.120115130 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.44
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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10,10-dimethyl-4-oxatricyclo(7.4.1.03,7)tetradeca-1,3(7),5,8,12-pentaene
10,10-Dimethyl-4-oxatricyclo[7.4.1.03,7]tetradeca-1,3(7),5,8,12-pentaene
RefChem:184696

2D Structure

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2D Structure of Spiniferin-1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8720 87.20%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4276 42.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9065 90.65%
OATP1B3 inhibitior + 0.9619 96.19%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6795 67.95%
P-glycoprotein inhibitior - 0.9544 95.44%
P-glycoprotein substrate - 0.8532 85.32%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8083 80.83%
CYP2D6 substrate - 0.7527 75.27%
CYP3A4 inhibition - 0.8971 89.71%
CYP2C9 inhibition - 0.6558 65.58%
CYP2C19 inhibition + 0.5622 56.22%
CYP2D6 inhibition - 0.7992 79.92%
CYP1A2 inhibition + 0.5536 55.36%
CYP2C8 inhibition - 0.7765 77.65%
CYP inhibitory promiscuity + 0.6613 66.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.4868 48.68%
Eye corrosion - 0.9285 92.85%
Eye irritation + 0.7514 75.14%
Skin irritation - 0.5947 59.47%
Skin corrosion - 0.9352 93.52%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6754 67.54%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.6035 60.35%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5753 57.53%
Acute Oral Toxicity (c) III 0.7304 73.04%
Estrogen receptor binding + 0.5423 54.23%
Androgen receptor binding + 0.6605 66.05%
Thyroid receptor binding - 0.7071 70.71%
Glucocorticoid receptor binding - 0.6003 60.03%
Aromatase binding + 0.7311 73.11%
PPAR gamma - 0.6380 63.80%
Honey bee toxicity - 0.8966 89.66%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9917 99.17%

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 94.33% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.16% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.26% 85.14%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.09% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.93% 95.56%
CHEMBL2581 P07339 Cathepsin D 82.56% 98.95%
CHEMBL4208 P20618 Proteasome component C5 81.35% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.13% 94.45%

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.
There are no matching plants.

Cross-Links

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PubChem 21637541
LOTUS LTS0247707
wikiData Q104402868