Harringtonolide

Details

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Internal ID a2261250-1905-45b1-a345-ae3d7357c2f4
Taxonomy Organoheterocyclic compounds > Furopyrans
IUPAC Name (1S,11S,12R,16R,19R)-8,19-dimethyl-14,17-dioxahexacyclo[13.3.1.01,11.04,10.09,13.012,16]nonadeca-4,7,9-triene-6,18-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O4/c1-7-5-10(20)6-9-3-4-19-8(2)15-17(23-18(19)21)13-14(19)12(9)11(7)16(13)22-15/h5-6,8,13-17H,3-4H2,1-2H3/t8-,13+,14+,15?,16?,17+,19+/m0/s1
InChI Key QNJIIOHVULPMRL-MBKAUVROSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O4
Molecular Weight 310.30 g/mol
Exact Mass 310.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 0.30
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Harringtonolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9833 98.33%
Caco-2 + 0.6401 64.01%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6638 66.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9121 91.21%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6669 66.69%
P-glycoprotein inhibitior - 0.7638 76.38%
P-glycoprotein substrate - 0.7809 78.09%
CYP3A4 substrate + 0.5982 59.82%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.8476 84.76%
CYP3A4 inhibition - 0.8225 82.25%
CYP2C9 inhibition - 0.7419 74.19%
CYP2C19 inhibition - 0.6182 61.82%
CYP2D6 inhibition - 0.8842 88.42%
CYP1A2 inhibition - 0.5953 59.53%
CYP2C8 inhibition - 0.8190 81.90%
CYP inhibitory promiscuity - 0.8501 85.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5408 54.08%
Eye corrosion - 0.9748 97.48%
Eye irritation - 0.9109 91.09%
Skin irritation - 0.6464 64.64%
Skin corrosion - 0.7338 73.38%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5608 56.08%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.7086 70.86%
skin sensitisation - 0.7797 77.97%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7719 77.19%
Acute Oral Toxicity (c) III 0.4770 47.70%
Estrogen receptor binding + 0.7595 75.95%
Androgen receptor binding + 0.7565 75.65%
Thyroid receptor binding - 0.6064 60.64%
Glucocorticoid receptor binding + 0.7024 70.24%
Aromatase binding - 0.7179 71.79%
PPAR gamma + 0.6351 63.51%
Honey bee toxicity - 0.8790 87.90%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9414 94.14%

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 94.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.57% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.61% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.85% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.40% 97.09%
CHEMBL230 P35354 Cyclooxygenase-2 86.83% 89.63%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.13% 89.00%
CHEMBL2581 P07339 Cathepsin D 85.48% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.24% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.95% 97.14%
CHEMBL4581 P52732 Kinesin-like protein 1 83.72% 93.18%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.52% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.31% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.28% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.17% 100.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.41% 85.11%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.98% 82.38%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.31% 93.03%
CHEMBL3401 O75469 Pregnane X receptor 80.07% 94.73%

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.
Cephalotaxus fortunei
Cephalotaxus hainanensis
Murraya paniculata

Cross-Links

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PubChem 56841078
NPASS NPC94048
LOTUS LTS0263379
wikiData Q104400164