8,12-Dihydroxy-3-(2-hydroxypropan-2-yl)-6a,12b-dimethyl-9-(4-methyl-3-oxohexan-2-yl)-8-(2-oxopropyl)-1,2,3,4a,5,6,12,12a-octahydropyrano[3,2-a]xanthen-11-one

Details

Top
Internal ID 101d6d6d-61c1-40fb-8980-90d41ec52103
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name 8,12-dihydroxy-3-(2-hydroxypropan-2-yl)-6a,12b-dimethyl-9-(4-methyl-3-oxohexan-2-yl)-8-(2-oxopropyl)-1,2,3,4a,5,6,12,12a-octahydropyrano[3,2-a]xanthen-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H46O8/c1-9-16(2)24(34)18(4)19-14-20(33)23-25(35)26-29(7)12-10-21(28(5,6)36)38-22(29)11-13-30(26,8)39-27(23)31(19,37)15-17(3)32/h14,16,18,21-22,25-26,35-37H,9-13,15H2,1-8H3
InChI Key ZCSZZICIPVOPHV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C31H46O8
Molecular Weight 546.70 g/mol
Exact Mass 546.31926842 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 3.60
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 8,12-Dihydroxy-3-(2-hydroxypropan-2-yl)-6a,12b-dimethyl-9-(4-methyl-3-oxohexan-2-yl)-8-(2-oxopropyl)-1,2,3,4a,5,6,12,12a-octahydropyrano[3,2-a]xanthen-11-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 - 0.7219 72.19%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7992 79.92%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8509 85.09%
OATP1B3 inhibitior + 0.8977 89.77%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6564 65.64%
BSEP inhibitior + 0.9569 95.69%
P-glycoprotein inhibitior + 0.7326 73.26%
P-glycoprotein substrate + 0.6475 64.75%
CYP3A4 substrate + 0.6923 69.23%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.8790 87.90%
CYP3A4 inhibition + 0.6407 64.07%
CYP2C9 inhibition - 0.9087 90.87%
CYP2C19 inhibition - 0.8879 88.79%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.9245 92.45%
CYP2C8 inhibition + 0.5487 54.87%
CYP inhibitory promiscuity - 0.9147 91.47%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5853 58.53%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.9273 92.73%
Skin irritation + 0.5621 56.21%
Skin corrosion - 0.9278 92.78%
Ames mutagenesis - 0.5324 53.24%
Human Ether-a-go-go-Related Gene inhibition - 0.4643 46.43%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5692 56.92%
skin sensitisation - 0.7998 79.98%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8111 81.11%
Acute Oral Toxicity (c) III 0.5651 56.51%
Estrogen receptor binding + 0.7102 71.02%
Androgen receptor binding + 0.7157 71.57%
Thyroid receptor binding - 0.5166 51.66%
Glucocorticoid receptor binding + 0.8161 81.61%
Aromatase binding + 0.8077 80.77%
PPAR gamma + 0.6428 64.28%
Honey bee toxicity - 0.8415 84.15%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9811 98.11%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.18% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.15% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.11% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.37% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 95.80% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 93.94% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.90% 94.45%
CHEMBL218 P21554 Cannabinoid CB1 receptor 91.45% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.44% 89.00%
CHEMBL230 P35354 Cyclooxygenase-2 91.13% 89.63%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.42% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.88% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.44% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.51% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.69% 95.89%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 84.96% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.30% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.47% 93.04%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 81.52% 92.78%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.08% 97.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.65% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.28% 97.09%

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.
There are no matching plants.

Cross-Links

Top
PubChem 163003476
LOTUS LTS0196822
wikiData Q104202295