Scodopin

Details

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Internal ID 4b8b1cb9-c444-465c-beb5-0b5c3c792fc7
Taxonomy Hydrocarbon derivatives > Tropones > Tropolones
IUPAC Name (1S,4R)-7-hydroxy-4-methyl-1-propan-2-yl-1,2,3,4-tetrahydrobenzo[7]annulen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O2/c1-9(2)11-5-4-10(3)13-8-15(17)14(16)7-6-12(11)13/h6-11H,4-5H2,1-3H3,(H,16,17)/t10-,11+/m1/s1
InChI Key UBBJWWNVYFBQMJ-MNOVXSKESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(1S,4R)-7-hydroxy-4-methyl-1-propan-2-yl-1,2,3,4-tetrahydrobenzo[7]annulen-6-one

2D Structure

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2D Structure of Scodopin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8915 89.15%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7373 73.73%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9567 95.67%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9249 92.49%
P-glycoprotein inhibitior - 0.9596 95.96%
P-glycoprotein substrate - 0.6365 63.65%
CYP3A4 substrate - 0.5511 55.11%
CYP2C9 substrate + 0.5969 59.69%
CYP2D6 substrate - 0.7493 74.93%
CYP3A4 inhibition - 0.9414 94.14%
CYP2C9 inhibition - 0.8313 83.13%
CYP2C19 inhibition - 0.8130 81.30%
CYP2D6 inhibition - 0.8871 88.71%
CYP1A2 inhibition + 0.8903 89.03%
CYP2C8 inhibition - 0.9355 93.55%
CYP inhibitory promiscuity - 0.9331 93.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6366 63.66%
Eye corrosion - 0.8748 87.48%
Eye irritation - 0.7182 71.82%
Skin irritation + 0.6446 64.46%
Skin corrosion - 0.5953 59.53%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5641 56.41%
Micronuclear - 0.9182 91.82%
Hepatotoxicity - 0.5684 56.84%
skin sensitisation + 0.7094 70.94%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7919 79.19%
Acute Oral Toxicity (c) III 0.8445 84.45%
Estrogen receptor binding - 0.8810 88.10%
Androgen receptor binding + 0.6220 62.20%
Thyroid receptor binding + 0.5259 52.59%
Glucocorticoid receptor binding - 0.5479 54.79%
Aromatase binding - 0.8074 80.74%
PPAR gamma - 0.5972 59.72%
Honey bee toxicity - 0.9657 96.57%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9645 96.45%

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
CHEMBL2581 P07339 Cathepsin D 95.97% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.87% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 95.17% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 94.16% 94.75%
CHEMBL1951 P21397 Monoamine oxidase A 93.51% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.20% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.04% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.62% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.34% 95.89%
CHEMBL5203 P33316 dUTP pyrophosphatase 87.90% 99.18%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.15% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.41% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.20% 93.03%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.89% 97.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.28% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.22% 93.40%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.12% 93.99%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.50% 90.24%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.88% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.82% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.21% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 80.75% 91.19%

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.
Scorodocarpus borneensis

Cross-Links

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PubChem 12051232
LOTUS LTS0091380
wikiData Q105269199