8Beta-Hydroxypachydictyol A

Details

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Internal ID 85ad4779-eaa0-4774-b342-c1b5b7a998f0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Pachydictyane and cneorubin diterpenoids
IUPAC Name (3aS,4S,5R,6R,8aR)-3-methyl-5-[(2R)-6-methylhept-5-en-2-yl]-8-methylidene-3a,4,5,6,7,8a-hexahydro-1H-azulene-4,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O2/c1-12(2)7-6-8-13(3)19-17(21)11-15(5)16-10-9-14(4)18(16)20(19)22/h7,9,13,16-22H,5-6,8,10-11H2,1-4H3/t13-,16+,17-,18-,19-,20+/m1/s1
InChI Key BKGLGOGPWGBWFY-AJTFGXLRSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O2
Molecular Weight 304.50 g/mol
Exact Mass 304.240230259 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL1652220

2D Structure

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2D Structure of 8Beta-Hydroxypachydictyol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.6721 67.21%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.5745 57.45%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8748 87.48%
OATP1B3 inhibitior + 0.9305 93.05%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5518 55.18%
P-glycoprotein inhibitior - 0.7648 76.48%
P-glycoprotein substrate - 0.6890 68.90%
CYP3A4 substrate + 0.5414 54.14%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate + 0.3479 34.79%
CYP3A4 inhibition - 0.7983 79.83%
CYP2C9 inhibition - 0.7980 79.80%
CYP2C19 inhibition - 0.7415 74.15%
CYP2D6 inhibition - 0.9173 91.73%
CYP1A2 inhibition - 0.6098 60.98%
CYP2C8 inhibition - 0.8983 89.83%
CYP inhibitory promiscuity - 0.6879 68.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6576 65.76%
Eye corrosion - 0.9715 97.15%
Eye irritation - 0.9223 92.23%
Skin irritation - 0.5114 51.14%
Skin corrosion - 0.9264 92.64%
Ames mutagenesis - 0.7678 76.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4293 42.93%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.5418 54.18%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6394 63.94%
Acute Oral Toxicity (c) I 0.3884 38.84%
Estrogen receptor binding - 0.6004 60.04%
Androgen receptor binding + 0.5483 54.83%
Thyroid receptor binding - 0.5121 51.21%
Glucocorticoid receptor binding - 0.5083 50.83%
Aromatase binding - 0.8536 85.36%
PPAR gamma - 0.6220 62.20%
Honey bee toxicity - 0.8530 85.30%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9656 96.56%

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 95.81% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.66% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 93.53% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 93.07% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.23% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.04% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.09% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.89% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.85% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.30% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.49% 95.56%

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 53325968
LOTUS LTS0152621
wikiData Q104937552