Rhodocorane A

Details

Top
Internal ID 9336af82-5537-4325-a2f4-50ffafaa5ed5
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 6-[(3S,3aR,5S,6R,6aS)-5-hydroxy-3,6-dimethyl-2,3,3a,4,5,6-hexahydrocyclopenta[b]furan-6a-yl]-3-hydroxy-4-methylpyran-2-one
SMILES (Canonical) CC1COC2(C1CC(C2C)O)C3=CC(=C(C(=O)O3)O)C
SMILES (Isomeric) C[C@@H]1CO[C@]2([C@@H]1C[C@@H]([C@H]2C)O)C3=CC(=C(C(=O)O3)O)C
InChI InChI=1S/C15H20O5/c1-7-4-12(20-14(18)13(7)17)15-9(3)11(16)5-10(15)8(2)6-19-15/h4,8-11,16-17H,5-6H2,1-3H3/t8-,9-,10-,11+,15-/m1/s1
InChI Key KMNBURIPCCDPIF-JAPZVGMSSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C15H20O5
Molecular Weight 280.32 g/mol
Exact Mass 280.13107373 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.53
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Rhodocorane A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9845 98.45%
Caco-2 + 0.7157 71.57%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7875 78.75%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8904 89.04%
OATP1B3 inhibitior + 0.9167 91.67%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7894 78.94%
P-glycoprotein inhibitior - 0.8519 85.19%
P-glycoprotein substrate - 0.6490 64.90%
CYP3A4 substrate + 0.6044 60.44%
CYP2C9 substrate + 0.6387 63.87%
CYP2D6 substrate - 0.8314 83.14%
CYP3A4 inhibition - 0.8138 81.38%
CYP2C9 inhibition - 0.9175 91.75%
CYP2C19 inhibition - 0.9305 93.05%
CYP2D6 inhibition - 0.9560 95.60%
CYP1A2 inhibition - 0.7107 71.07%
CYP2C8 inhibition - 0.8001 80.01%
CYP inhibitory promiscuity - 0.9487 94.87%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5774 57.74%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9110 91.10%
Skin irritation - 0.7290 72.90%
Skin corrosion - 0.9404 94.04%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6716 67.16%
Micronuclear - 0.6641 66.41%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation - 0.8394 83.94%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8777 87.77%
Acute Oral Toxicity (c) III 0.4227 42.27%
Estrogen receptor binding + 0.5846 58.46%
Androgen receptor binding + 0.7108 71.08%
Thyroid receptor binding + 0.5179 51.79%
Glucocorticoid receptor binding + 0.7287 72.87%
Aromatase binding - 0.5603 56.03%
PPAR gamma - 0.5353 53.53%
Honey bee toxicity - 0.8156 81.56%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9710 97.10%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.08% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.26% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.99% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.79% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.90% 98.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.66% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.48% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.00% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.56% 97.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.90% 85.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.72% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.65% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 82.98% 91.49%
CHEMBL4530 P00488 Coagulation factor XIII 82.18% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.54% 95.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.21% 93.04%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.75% 97.21%

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 146683190
LOTUS LTS0259185
wikiData Q105143047