4,8,14-Trihydroxyilludala-2,6,8-triene

Details

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Internal ID 6d2ab69f-3b47-4eba-a003-b596fa3cdf0c
Taxonomy Benzenoids > Indanes
IUPAC Name (2S)-6-(2-hydroxyethyl)-2-(hydroxymethyl)-2,5,7-trimethyl-1,3-dihydroinden-4-ol
SMILES (Canonical) CC1=C2CC(CC2=C(C(=C1CCO)C)O)(C)CO
SMILES (Isomeric) CC1=C2C[C@](CC2=C(C(=C1CCO)C)O)(C)CO
InChI InChI=1S/C15H22O3/c1-9-11(4-5-16)10(2)14(18)13-7-15(3,8-17)6-12(9)13/h16-18H,4-8H2,1-3H3/t15-/m0/s1
InChI Key FCSXZAGMYKCEHI-HNNXBMFYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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4,8,14-Trihydroxyilludala-2,6,8-triene

2D Structure

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2D Structure of 4,8,14-Trihydroxyilludala-2,6,8-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.9111 91.11%
Blood Brain Barrier + 0.6385 63.85%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7277 72.77%
OATP2B1 inhibitior - 0.8453 84.53%
OATP1B1 inhibitior + 0.8293 82.93%
OATP1B3 inhibitior + 0.8948 89.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7852 78.52%
BSEP inhibitior - 0.8157 81.57%
P-glycoprotein inhibitior - 0.9216 92.16%
P-glycoprotein substrate - 0.8282 82.82%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate + 0.3802 38.02%
CYP3A4 inhibition - 0.7083 70.83%
CYP2C9 inhibition - 0.8545 85.45%
CYP2C19 inhibition - 0.8687 86.87%
CYP2D6 inhibition - 0.9574 95.74%
CYP1A2 inhibition + 0.5330 53.30%
CYP2C8 inhibition - 0.7155 71.55%
CYP inhibitory promiscuity - 0.8508 85.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6216 62.16%
Eye corrosion - 0.9901 99.01%
Eye irritation + 0.9577 95.77%
Skin irritation - 0.6916 69.16%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5236 52.36%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8028 80.28%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6037 60.37%
Acute Oral Toxicity (c) III 0.7119 71.19%
Estrogen receptor binding - 0.6000 60.00%
Androgen receptor binding - 0.4816 48.16%
Thyroid receptor binding - 0.5176 51.76%
Glucocorticoid receptor binding + 0.5886 58.86%
Aromatase binding - 0.6674 66.74%
PPAR gamma - 0.5643 56.43%
Honey bee toxicity - 0.9432 94.32%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9528 95.28%

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 91.91% 91.11%
CHEMBL240 Q12809 HERG 87.69% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.18% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.72% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.43% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 82.07% 94.75%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.20% 98.75%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 80.09% 85.49%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 12040220
LOTUS LTS0008243
wikiData Q75060002