(4R,7S)-7,14-dihydroxy-16-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one

Details

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Internal ID 8759a658-14d6-4471-b155-69f4bc19a8ef
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (4R,7S)-7,14-dihydroxy-16-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one
SMILES (Canonical) CC1CCC(CCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O
SMILES (Isomeric) C[C@@H]1CC[C@H](CCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O
InChI InChI=1S/C17H24O5/c1-11-7-8-13(18)6-4-3-5-12-9-14(19)10-15(21-2)16(12)17(20)22-11/h9-11,13,18-19H,3-8H2,1-2H3/t11-,13+/m1/s1
InChI Key DGMDZTUKWDQSTB-YPMHNXCESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O5
Molecular Weight 308.40 g/mol
Exact Mass 308.16237386 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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(3R,6S)-6-Hydroxylasiodiplodin

2D Structure

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2D Structure of (4R,7S)-7,14-dihydroxy-16-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.7778 77.78%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7563 75.63%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8954 89.54%
OATP1B3 inhibitior + 0.9217 92.17%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9571 95.71%
BSEP inhibitior - 0.7669 76.69%
P-glycoprotein inhibitior - 0.8662 86.62%
P-glycoprotein substrate - 0.8498 84.98%
CYP3A4 substrate + 0.6168 61.68%
CYP2C9 substrate - 0.5773 57.73%
CYP2D6 substrate - 0.7857 78.57%
CYP3A4 inhibition - 0.6472 64.72%
CYP2C9 inhibition - 0.9166 91.66%
CYP2C19 inhibition - 0.7467 74.67%
CYP2D6 inhibition - 0.8622 86.22%
CYP1A2 inhibition + 0.7884 78.84%
CYP2C8 inhibition - 0.5834 58.34%
CYP inhibitory promiscuity - 0.9457 94.57%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8611 86.11%
Carcinogenicity (trinary) Non-required 0.7062 70.62%
Eye corrosion - 0.9765 97.65%
Eye irritation - 0.8863 88.63%
Skin irritation - 0.7361 73.61%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6813 68.13%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6020 60.20%
skin sensitisation - 0.8473 84.73%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7538 75.38%
Acute Oral Toxicity (c) III 0.4213 42.13%
Estrogen receptor binding + 0.7312 73.12%
Androgen receptor binding + 0.6351 63.51%
Thyroid receptor binding - 0.6207 62.07%
Glucocorticoid receptor binding + 0.6499 64.99%
Aromatase binding - 0.5176 51.76%
PPAR gamma + 0.6678 66.78%
Honey bee toxicity - 0.8761 87.61%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.9474 94.74%

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 98.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.30% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 95.67% 91.49%
CHEMBL2581 P07339 Cathepsin D 94.51% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.73% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.27% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.04% 96.09%
CHEMBL2535 P11166 Glucose transporter 89.96% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.54% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.42% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.63% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.48% 97.14%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 85.73% 82.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.59% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.28% 99.18%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.14% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.99% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.04% 99.17%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.72% 91.07%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.21% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.18% 94.45%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.39% 94.03%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.85% 95.78%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.70% 90.71%

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.
Carthamus arborescens

Cross-Links

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PubChem 101765495
NPASS NPC51106
LOTUS LTS0255661
wikiData Q104978904