(2R,4S,5'S,6S,7S,10S,12S)-5',12,17-trihydroxy-6-methylspiro[3,8-dioxahexacyclo[11.8.0.02,4.02,10.06,10.014,19]henicosa-1(13),14(19),15,17-tetraene-7,4'-oxolane]-2',20-dione

Details

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Internal ID b23e6d0b-e104-4904-8194-c6bf3a3a1ef2
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (2R,4S,5'S,6S,7S,10S,12S)-5',12,17-trihydroxy-6-methylspiro[3,8-dioxahexacyclo[11.8.0.02,4.02,10.06,10.014,19]henicosa-1(13),14(19),15,17-tetraene-7,4'-oxolane]-2',20-dione
SMILES (Canonical) CC12CC3C4(C1(CC(C5=C4CC(=O)C6=C5C=CC(=C6)O)O)COC27CC(=O)OC7O)O3
SMILES (Isomeric) C[C@]12C[C@H]3[C@@]4([C@]1(C[C@@H](C5=C4CC(=O)C6=C5C=CC(=C6)O)O)CO[C@@]27CC(=O)O[C@@H]7O)O3
InChI InChI=1S/C23H22O8/c1-20-7-16-23(31-16)13-5-14(25)12-4-10(24)2-3-11(12)18(13)15(26)6-21(20,23)9-29-22(20)8-17(27)30-19(22)28/h2-4,15-16,19,24,26,28H,5-9H2,1H3/t15-,16-,19-,20-,21+,22+,23-/m0/s1
InChI Key JDNHANBRNDZELM-FACWNCDSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O8
Molecular Weight 426.40 g/mol
Exact Mass 426.13146766 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP -1.00
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,4S,5'S,6S,7S,10S,12S)-5',12,17-trihydroxy-6-methylspiro[3,8-dioxahexacyclo[11.8.0.02,4.02,10.06,10.014,19]henicosa-1(13),14(19),15,17-tetraene-7,4'-oxolane]-2',20-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 - 0.7354 73.54%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8315 83.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8090 80.90%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7864 78.64%
BSEP inhibitior + 0.6726 67.26%
P-glycoprotein inhibitior - 0.5727 57.27%
P-glycoprotein substrate + 0.6803 68.03%
CYP3A4 substrate + 0.6603 66.03%
CYP2C9 substrate - 0.8066 80.66%
CYP2D6 substrate - 0.8496 84.96%
CYP3A4 inhibition - 0.7144 71.44%
CYP2C9 inhibition - 0.7080 70.80%
CYP2C19 inhibition - 0.7520 75.20%
CYP2D6 inhibition - 0.8600 86.00%
CYP1A2 inhibition - 0.6467 64.67%
CYP2C8 inhibition + 0.5393 53.93%
CYP inhibitory promiscuity - 0.8999 89.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4366 43.66%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.9085 90.85%
Skin irritation - 0.6689 66.89%
Skin corrosion - 0.9301 93.01%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5905 59.05%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.6420 64.20%
skin sensitisation - 0.7971 79.71%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.6837 68.37%
Acute Oral Toxicity (c) I 0.4276 42.76%
Estrogen receptor binding + 0.8777 87.77%
Androgen receptor binding + 0.7375 73.75%
Thyroid receptor binding + 0.5363 53.63%
Glucocorticoid receptor binding + 0.7587 75.87%
Aromatase binding + 0.7919 79.19%
PPAR gamma + 0.7067 70.67%
Honey bee toxicity - 0.6830 68.30%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9940 99.40%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.30% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.43% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.25% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 92.91% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.43% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.67% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.49% 89.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.99% 90.17%
CHEMBL240 Q12809 HERG 87.93% 89.76%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.75% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.95% 85.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.69% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.42% 97.09%
CHEMBL4208 P20618 Proteasome component C5 83.32% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.21% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.83% 95.89%
CHEMBL242 Q92731 Estrogen receptor beta 81.32% 98.35%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.29% 97.14%

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.
There are no matching plants.

Cross-Links

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PubChem 162869850
LOTUS LTS0112134
wikiData Q105125603