dihydro ochraceolide A

Details

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Internal ID 37e82443-6cff-41a5-a5c1-5b640011b232
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,2R,5R,7S,10R,11R,14R,15S,16R,20R,22S)-7-hydroxy-1,2,6,6,10,22-hexamethyl-17-methylidene-19-oxahexacyclo[12.10.0.02,11.05,10.015,22.016,20]tetracosan-18-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H46O3/c1-17-23-19(33-25(17)32)16-27(4)14-15-29(6)18(24(23)27)8-9-21-28(5)12-11-22(31)26(2,3)20(28)10-13-30(21,29)7/h18-24,31H,1,8-16H2,2-7H3/t18-,19-,20+,21-,22+,23-,24+,27+,28+,29-,30-/m1/s1
InChI Key MPHDAXXJNDNMGF-MRRHYTQVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H46O3
Molecular Weight 454.70 g/mol
Exact Mass 454.34469533 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 8.00
Atomic LogP (AlogP) 6.54
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL512958

2D Structure

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2D Structure of dihydro ochraceolide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 - 0.6306 63.06%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7598 75.98%
OATP2B1 inhibitior - 0.7089 70.89%
OATP1B1 inhibitior + 0.9073 90.73%
OATP1B3 inhibitior - 0.2436 24.36%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.6779 67.79%
P-glycoprotein inhibitior - 0.6314 63.14%
P-glycoprotein substrate - 0.8609 86.09%
CYP3A4 substrate + 0.6945 69.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8379 83.79%
CYP3A4 inhibition + 0.5319 53.19%
CYP2C9 inhibition - 0.8430 84.30%
CYP2C19 inhibition - 0.6515 65.15%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.7508 75.08%
CYP2C8 inhibition - 0.6541 65.41%
CYP inhibitory promiscuity - 0.8731 87.31%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5855 58.55%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9148 91.48%
Skin irritation + 0.6028 60.28%
Skin corrosion - 0.9239 92.39%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6872 68.72%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.6059 60.59%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity + 0.6346 63.46%
Acute Oral Toxicity (c) III 0.6398 63.98%
Estrogen receptor binding + 0.7054 70.54%
Androgen receptor binding + 0.7515 75.15%
Thyroid receptor binding + 0.6407 64.07%
Glucocorticoid receptor binding + 0.7807 78.07%
Aromatase binding + 0.7038 70.38%
PPAR gamma + 0.6542 65.42%
Honey bee toxicity - 0.6474 64.74%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9961 99.61%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.93% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.36% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.61% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.08% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.02% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.68% 95.89%
CHEMBL204 P00734 Thrombin 86.83% 96.01%
CHEMBL221 P23219 Cyclooxygenase-1 86.27% 90.17%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.89% 93.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.28% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.82% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.49% 99.23%

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.
Lophopetalum wallichii

Cross-Links

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PubChem 44566890
LOTUS LTS0263987
wikiData Q105169511