Agariblazeispirol A

Details

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Internal ID 1e2781f9-573b-4e1b-86e2-9451f9739229
Taxonomy Benzenoids > Naphthalenes
IUPAC Name (1S,3'R,4'S,10R,13R,14S,15R)-6-methoxy-4',5,5',5',10,14-hexamethylspiro[16-oxatetracyclo[8.6.0.01,13.04,9]hexadeca-2,4(9),5,7-tetraene-15,2'-oxolane]-3'-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H34O4/c1-14-17-10-13-24-18(11-12-23(24,6)19(17)8-9-20(14)27-7)15(2)25(29-24)21(26)16(3)22(4,5)28-25/h8-10,13,15-16,18,21,26H,11-12H2,1-7H3/t15-,16-,18+,21+,23+,24-,25+/m0/s1
InChI Key XANOSTKMMIEIMI-XJOOGWOKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H34O4
Molecular Weight 398.50 g/mol
Exact Mass 398.24570956 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.61
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Agariblazeispirol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.5902 59.02%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5995 59.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8581 85.81%
OATP1B3 inhibitior + 0.8616 86.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7416 74.16%
P-glycoprotein inhibitior - 0.6099 60.99%
P-glycoprotein substrate - 0.5562 55.62%
CYP3A4 substrate + 0.6798 67.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7282 72.82%
CYP3A4 inhibition - 0.5067 50.67%
CYP2C9 inhibition - 0.6734 67.34%
CYP2C19 inhibition - 0.6710 67.10%
CYP2D6 inhibition - 0.7933 79.33%
CYP1A2 inhibition - 0.5400 54.00%
CYP2C8 inhibition + 0.5714 57.14%
CYP inhibitory promiscuity - 0.5485 54.85%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Danger 0.5274 52.74%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9291 92.91%
Skin irritation - 0.7092 70.92%
Skin corrosion - 0.9091 90.91%
Ames mutagenesis - 0.6570 65.70%
Human Ether-a-go-go-Related Gene inhibition - 0.3915 39.15%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5779 57.79%
skin sensitisation - 0.7704 77.04%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8404 84.04%
Acute Oral Toxicity (c) III 0.4708 47.08%
Estrogen receptor binding + 0.8612 86.12%
Androgen receptor binding + 0.7175 71.75%
Thyroid receptor binding + 0.8481 84.81%
Glucocorticoid receptor binding + 0.7555 75.55%
Aromatase binding + 0.7871 78.71%
PPAR gamma + 0.5980 59.80%
Honey bee toxicity - 0.8719 87.19%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9852 98.52%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.59% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.04% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.03% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.90% 97.09%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 88.56% 89.05%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.39% 95.56%
CHEMBL1871 P10275 Androgen Receptor 86.82% 96.43%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.72% 89.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.35% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.52% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.28% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.05% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.66% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.52% 100.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.10% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.52% 97.25%

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 10250287
LOTUS LTS0198141
wikiData Q77424881