Dihydroamoorinin

Details

Top
Internal ID db2383ab-f9fd-4cb0-82de-ef4c961bda5b
Taxonomy Organoheterocyclic compounds > Dioxepanes > 1,4-dioxepanes
IUPAC Name methyl 2-[(1R,3S,6R)-6-[(1aS,4R,4aS,7R,8aS)-4-(furan-3-yl)-4a-methyl-8-methylidene-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromen-7-yl]-3-hydroxy-2,2,6-trimethylcyclohexyl]acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H36O7/c1-15-17(25(4)10-8-19(28)24(2,3)18(25)13-20(29)31-6)7-11-26(5)21(16-9-12-32-14-16)33-23(30)22-27(15,26)34-22/h9,12,14,17-19,21-22,28H,1,7-8,10-11,13H2,2-6H3/t17-,18-,19-,21+,22+,25-,26-,27+/m0/s1
InChI Key BOBVUKUEMMUUKW-UOKFWGLMSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H36O7
Molecular Weight 472.60 g/mol
Exact Mass 472.24610348 g/mol
Topological Polar Surface Area (TPSA) 98.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.35
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Dihydroamoorinin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9808 98.08%
Caco-2 - 0.6874 68.74%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7281 72.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.4146 41.46%
OATP1B3 inhibitior - 0.2797 27.97%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8418 84.18%
P-glycoprotein inhibitior + 0.6718 67.18%
P-glycoprotein substrate + 0.5465 54.65%
CYP3A4 substrate + 0.7185 71.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8347 83.47%
CYP3A4 inhibition + 0.8854 88.54%
CYP2C9 inhibition - 0.5880 58.80%
CYP2C19 inhibition - 0.6724 67.24%
CYP2D6 inhibition - 0.9172 91.72%
CYP1A2 inhibition - 0.7490 74.90%
CYP2C8 inhibition + 0.6450 64.50%
CYP inhibitory promiscuity - 0.8416 84.16%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5743 57.43%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.8891 88.91%
Skin irritation - 0.6385 63.85%
Skin corrosion - 0.9240 92.40%
Ames mutagenesis - 0.7470 74.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7106 71.06%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5145 51.45%
skin sensitisation - 0.8318 83.18%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7478 74.78%
Acute Oral Toxicity (c) I 0.5564 55.64%
Estrogen receptor binding + 0.7081 70.81%
Androgen receptor binding + 0.7602 76.02%
Thyroid receptor binding + 0.6413 64.13%
Glucocorticoid receptor binding + 0.8021 80.21%
Aromatase binding + 0.8025 80.25%
PPAR gamma + 0.6645 66.45%
Honey bee toxicity - 0.8184 81.84%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9962 99.62%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.59% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 91.92% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.25% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.78% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.44% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.16% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.99% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.92% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.95% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.19% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 85.12% 83.82%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.87% 94.33%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.15% 97.28%
CHEMBL3524 P56524 Histone deacetylase 4 83.02% 92.97%
CHEMBL2581 P07339 Cathepsin D 80.99% 98.95%

Plants that contains it

Top
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.
Aphanamixis polystachya

Cross-Links

Top
PubChem 15508011
LOTUS LTS0065949
wikiData Q104939147