Abyssomicin S

Details

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Internal ID 9dde3243-4336-4570-9a3f-74d3d8838293
Taxonomy Organoheterocyclic compounds > Furopyrans
IUPAC Name (1R,2S,3S,4S,5R,7S,9S,14S,16R,18R)-2,4,7,10,16-pentahydroxy-1,7,9,16-tetramethyl-13,17-dioxapentacyclo[9.5.2.03,14.05,18.014,18]octadec-10-ene-6,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26O9/c1-7-5-16(2,26)13(23)9-12(22)8-14(24)18(4)17(3,27)6-19(8)20(9,29-18)10(11(7)21)15(25)28-19/h7-9,12,14,21-22,24,26-27H,5-6H2,1-4H3/t7-,8-,9-,12-,14-,16-,17+,18+,19-,20+/m0/s1
InChI Key NAYVDWJFVXWOFH-YWNJRVHOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O9
Molecular Weight 410.40 g/mol
Exact Mass 410.15768240 g/mol
Topological Polar Surface Area (TPSA) 154.00 Ų
XlogP -1.70
Atomic LogP (AlogP) -0.90
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Abyssomicin S

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9682 96.82%
Caco-2 - 0.6529 65.29%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6127 61.27%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.8658 86.58%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9092 90.92%
P-glycoprotein inhibitior - 0.7290 72.90%
P-glycoprotein substrate - 0.6031 60.31%
CYP3A4 substrate + 0.6788 67.88%
CYP2C9 substrate - 0.8020 80.20%
CYP2D6 substrate - 0.8767 87.67%
CYP3A4 inhibition - 0.7441 74.41%
CYP2C9 inhibition - 0.8829 88.29%
CYP2C19 inhibition - 0.9174 91.74%
CYP2D6 inhibition - 0.9294 92.94%
CYP1A2 inhibition - 0.8975 89.75%
CYP2C8 inhibition - 0.6237 62.37%
CYP inhibitory promiscuity - 0.9057 90.57%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4968 49.68%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.8895 88.95%
Skin irritation + 0.4947 49.47%
Skin corrosion - 0.8812 88.12%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6787 67.87%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.5082 50.82%
skin sensitisation - 0.8108 81.08%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.8369 83.69%
Acute Oral Toxicity (c) I 0.4702 47.02%
Estrogen receptor binding + 0.7660 76.60%
Androgen receptor binding + 0.6867 68.67%
Thyroid receptor binding + 0.6552 65.52%
Glucocorticoid receptor binding + 0.6358 63.58%
Aromatase binding + 0.5862 58.62%
PPAR gamma + 0.5565 55.65%
Honey bee toxicity - 0.8262 82.62%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9379 93.79%

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 97.77% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.02% 91.49%
CHEMBL2581 P07339 Cathepsin D 94.95% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.38% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.53% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.84% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.89% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 86.74% 90.17%
CHEMBL1937 Q92769 Histone deacetylase 2 85.33% 94.75%
CHEMBL4208 P20618 Proteasome component C5 85.05% 90.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.96% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.70% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.49% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.06% 92.94%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.78% 97.14%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.30% 91.24%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139589691
LOTUS LTS0188025
wikiData Q105176651