Deoxyartemisinin

Details

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Internal ID bf19d866-d870-4d09-a4a0-02aa9819f89c
Taxonomy Organoheterocyclic compounds > Dioxolopyrans
IUPAC Name (1S,4S,5R,8S,9R,12S,13R)-1,5,9-trimethyl-11,14,15-trioxatetracyclo[10.2.1.04,13.08,13]pentadecan-10-one
SMILES (Canonical) CC1CCC2C(C(=O)OC3C24C1CCC(O3)(O4)C)C
SMILES (Isomeric) C[C@@H]1CC[C@H]2[C@H](C(=O)O[C@H]3[C@@]24[C@H]1CC[C@](O3)(O4)C)C
InChI InChI=1S/C15H22O4/c1-8-4-5-11-9(2)12(16)17-13-15(11)10(8)6-7-14(3,18-13)19-15/h8-11,13H,4-7H2,1-3H3/t8-,9-,10+,11+,13-,14-,15-/m1/s1
InChI Key ZQGMLVQZBIKKMP-NNWCWBAJSA-N
Popularity 26 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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72826-63-2
Deoxy Artemisinin
2-deoxyartemisinin
(3R,3AS,3a1R,6R,6aS,9S,10aS)-3,6,9-trimethyldecahydro-2H-3a1,9-epoxyoxepino[4,3,2-ij]isochromen-2-one
UNII-J59T2407WZ
J59T2407WZ
(1S,4S,5R,8S,9R,12S,13R)-1,5,9-trimethyl-11,14,15-trioxatetracyclo[10.2.1.04,13.08,13]pentadecan-10-one
Desoxyartemisinin
Hydroarteannuin
Artemisinin, deoxy
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Deoxyartemisinin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9729 97.29%
Caco-2 + 0.9195 91.95%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6182 61.82%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9244 92.44%
OATP1B3 inhibitior + 0.9736 97.36%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8854 88.54%
P-glycoprotein inhibitior - 0.8334 83.34%
P-glycoprotein substrate - 0.9265 92.65%
CYP3A4 substrate + 0.7008 70.08%
CYP2C9 substrate - 0.8521 85.21%
CYP2D6 substrate - 0.8409 84.09%
CYP3A4 inhibition - 0.9092 90.92%
CYP2C9 inhibition - 0.9468 94.68%
CYP2C19 inhibition - 0.8659 86.59%
CYP2D6 inhibition - 0.9562 95.62%
CYP1A2 inhibition + 0.5461 54.61%
CYP2C8 inhibition - 0.7974 79.74%
CYP inhibitory promiscuity - 0.9744 97.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6156 61.56%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8697 86.97%
Skin irritation - 0.5710 57.10%
Skin corrosion - 0.7783 77.83%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6850 68.50%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8700 87.00%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4699 46.99%
Acute Oral Toxicity (c) III 0.4316 43.16%
Estrogen receptor binding + 0.7389 73.89%
Androgen receptor binding + 0.7974 79.74%
Thyroid receptor binding + 0.6501 65.01%
Glucocorticoid receptor binding + 0.6432 64.32%
Aromatase binding - 0.5495 54.95%
PPAR gamma + 0.5203 52.03%
Honey bee toxicity - 0.7673 76.73%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9462 94.62%

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
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.03% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.73% 96.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.47% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.66% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.27% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.08% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.52% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.34% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.02% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.54% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.51% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.08% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 81.66% 92.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.02% 96.61%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.62% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.61% 86.33%

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.
Artemisia annua
Artemisia carvifolia

Cross-Links

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PubChem 12814879
NPASS NPC60568
ChEMBL CHEMBL331309
LOTUS LTS0090782
wikiData Q27281229