Haemodorose

Details

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Internal ID 86f004a5-bab7-4934-898c-f4869282e157
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 7-methoxy-10-phenyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-oxatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-2-one
SMILES (Canonical) COC1=C(C2=C(C=CC3=C2C(=C1)COC3=O)C4=CC=CC=C4)OC5C(C(C(C(O5)CO)O)O)O
SMILES (Isomeric) COC1=C(C2=C(C=CC3=C2C(=C1)COC3=O)C4=CC=CC=C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O
InChI InChI=1S/C25H24O9/c1-31-16-9-13-11-32-24(30)15-8-7-14(12-5-3-2-4-6-12)19(18(13)15)23(16)34-25-22(29)21(28)20(27)17(10-26)33-25/h2-9,17,20-22,25-29H,10-11H2,1H3/t17-,20-,21+,22-,25+/m1/s1
InChI Key PZTAHEJWBGPZLJ-FHBCLOHASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O9
Molecular Weight 468.50 g/mol
Exact Mass 468.14203234 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.36
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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CHEMBL552207

2D Structure

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2D Structure of Haemodorose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5457 54.57%
Caco-2 - 0.8118 81.18%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.5961 59.61%
OATP2B1 inhibitior - 0.7080 70.80%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.9786 97.86%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9537 95.37%
P-glycoprotein inhibitior - 0.5510 55.10%
P-glycoprotein substrate - 0.6974 69.74%
CYP3A4 substrate + 0.6235 62.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8385 83.85%
CYP3A4 inhibition - 0.9437 94.37%
CYP2C9 inhibition - 0.9060 90.60%
CYP2C19 inhibition - 0.8926 89.26%
CYP2D6 inhibition - 0.9515 95.15%
CYP1A2 inhibition - 0.9150 91.50%
CYP2C8 inhibition + 0.4784 47.84%
CYP inhibitory promiscuity - 0.7142 71.42%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6642 66.42%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9443 94.43%
Skin irritation - 0.8320 83.20%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4564 45.64%
Micronuclear + 0.6533 65.33%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.9324 93.24%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6498 64.98%
Acute Oral Toxicity (c) III 0.6678 66.78%
Estrogen receptor binding + 0.7814 78.14%
Androgen receptor binding + 0.7283 72.83%
Thyroid receptor binding - 0.5974 59.74%
Glucocorticoid receptor binding + 0.5761 57.61%
Aromatase binding - 0.4849 48.49%
PPAR gamma + 0.6976 69.76%
Honey bee toxicity - 0.7880 78.80%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5151 51.51%
Fish aquatic toxicity + 0.6698 66.98%

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
CHEMBL2581 P07339 Cathepsin D 97.85% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.04% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.46% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.55% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.34% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 92.83% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.57% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.73% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.43% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.47% 97.14%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 85.40% 95.83%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.58% 96.21%
CHEMBL1951 P21397 Monoamine oxidase A 80.60% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.39% 97.09%
CHEMBL1907 P15144 Aminopeptidase N 80.24% 93.31%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.05% 95.89%

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.
Haemodorum simplex
Saururus chinensis

Cross-Links

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PubChem 44179651
NPASS NPC52598
LOTUS LTS0170572
wikiData Q105217106