Anhydrodebromaplysiatoxin

Details

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Internal ID 212912ee-af6d-4c93-bb20-053c72e4d5fe
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (1S,3R,4S,5S,9R)-9-[(1R)-1-hydroxyethyl]-3-[(2S,5S)-5-(3-hydroxyphenyl)-5-methoxypentan-2-yl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadec-13-ene-7,11-dione
SMILES (Canonical) CC1C2CC3(C(CC(=C(O3)CC(=O)OC(CC(=O)O2)C(C)O)C)(C)C)OC1C(C)CCC(C4=CC(=CC=C4)O)OC
SMILES (Isomeric) C[C@H]1[C@@H]2C[C@]3(C(CC(=C(O3)CC(=O)O[C@H](CC(=O)O2)[C@@H](C)O)C)(C)C)O[C@@H]1[C@@H](C)CC[C@@H](C4=CC(=CC=C4)O)OC
InChI InChI=1S/C32H46O9/c1-18(11-12-24(37-7)22-9-8-10-23(34)13-22)30-20(3)27-17-32(41-30)31(5,6)16-19(2)25(40-32)14-28(35)38-26(21(4)33)15-29(36)39-27/h8-10,13,18,20-21,24,26-27,30,33-34H,11-12,14-17H2,1-7H3/t18-,20-,21+,24-,26+,27-,30+,32+/m0/s1
InChI Key HCEQACRMJXGKHI-UOYYIASUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H46O9
Molecular Weight 574.70 g/mol
Exact Mass 574.31418304 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 5.34
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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Anhydro-
Anhydrodebromaplysiatoxin
NSC-694448

2D Structure

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2D Structure of Anhydrodebromaplysiatoxin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9818 98.18%
Caco-2 - 0.7879 78.79%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7985 79.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8449 84.49%
OATP1B3 inhibitior - 0.4817 48.17%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8590 85.90%
P-glycoprotein inhibitior + 0.7389 73.89%
P-glycoprotein substrate + 0.7227 72.27%
CYP3A4 substrate + 0.7130 71.30%
CYP2C9 substrate - 0.7935 79.35%
CYP2D6 substrate - 0.8444 84.44%
CYP3A4 inhibition - 0.6459 64.59%
CYP2C9 inhibition - 0.8077 80.77%
CYP2C19 inhibition - 0.8155 81.55%
CYP2D6 inhibition - 0.9297 92.97%
CYP1A2 inhibition - 0.7365 73.65%
CYP2C8 inhibition + 0.5811 58.11%
CYP inhibitory promiscuity - 0.8769 87.69%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5821 58.21%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9356 93.56%
Skin irritation - 0.6855 68.55%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4151 41.51%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6159 61.59%
skin sensitisation - 0.8313 83.13%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6940 69.40%
Acute Oral Toxicity (c) III 0.3056 30.56%
Estrogen receptor binding + 0.7829 78.29%
Androgen receptor binding + 0.6748 67.48%
Thyroid receptor binding + 0.5752 57.52%
Glucocorticoid receptor binding + 0.7978 79.78%
Aromatase binding + 0.6806 68.06%
PPAR gamma + 0.7846 78.46%
Honey bee toxicity - 0.6635 66.35%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9941 99.41%

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
CHEMBL240 Q12809 HERG 99.48% 89.76%
CHEMBL2581 P07339 Cathepsin D 98.95% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.31% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.69% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.20% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.64% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.25% 95.56%
CHEMBL236 P41143 Delta opioid receptor 95.85% 99.35%
CHEMBL2996 Q05655 Protein kinase C delta 94.67% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.29% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.76% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.15% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.57% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.17% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.99% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 86.75% 94.73%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.70% 93.40%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.52% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.37% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.61% 99.15%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.01% 100.00%
CHEMBL4208 P20618 Proteasome component C5 82.77% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.22% 96.95%
CHEMBL233 P35372 Mu opioid receptor 81.90% 97.93%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.87% 97.14%
CHEMBL1907 P15144 Aminopeptidase N 80.94% 93.31%

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.
Cinnamomum camphora

Cross-Links

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PubChem 393063
NPASS NPC295196
LOTUS LTS0128774
wikiData Q105025643