16-Hydroxytriptolide

Details

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Internal ID 498f0760-70ee-41ee-885e-dfaee4e1b9c2
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (1S,2S,4S,5S,7R,8R,9S,11S,13S)-8-hydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1-methyl-3,6,10,16-tetraoxaheptacyclo[11.7.0.02,4.02,9.05,7.09,11.014,18]icos-14(18)-en-17-one
SMILES (Canonical) CC(CO)C12C(O1)C3C4(O3)C5(CCC6=C(C5CC7C4(C2O)O7)COC6=O)C
SMILES (Isomeric) C[C@@H](CO)[C@@]12[C@@H](O1)[C@H]3[C@@]4(O3)[C@]5(CCC6=C([C@@H]5C[C@H]7[C@]4([C@@H]2O)O7)COC6=O)C
InChI InChI=1S/C20H24O7/c1-8(6-21)18-13(26-18)14-20(27-14)17(2)4-3-9-10(7-24-15(9)22)11(17)5-12-19(20,25-12)16(18)23/h8,11-14,16,21,23H,3-7H2,1-2H3/t8-,11-,12-,13-,14-,16+,17-,18-,19+,20+/m0/s1
InChI Key HPTCYMNPHWXVLA-UBBHAYRHSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O7
Molecular Weight 376.40 g/mol
Exact Mass 376.15220310 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP -1.00
Atomic LogP (AlogP) 0.08
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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139713-80-7
(15S)-16-Hydroxytriptolide
(1S,2S,4S,5S,7R,8R,9S,11S,13S)-8-hydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1-methyl-3,6,10,16-tetraoxaheptacyclo[11.7.0.02,4.02,9.05,7.09,11.014,18]icos-14(18)-en-17-one
DTXSID70930562
CHEBI:132621
Triptolide, 16-hydroxy-, (15S)-
(3bS,4aS,5aS,6R,6aR,7aS,7bS,8aS,8bS)-6-hydroxy-6a-[(2S)-1-hydroxypropan-2-yl]-8b-methyl-3b,4,4a,6,6a,7a,7b,8b,9,10-decahydrotrisoxireno[6,7:8a,9:4b,5]phenanthro[1,2-c]furan-1(3H)-one

2D Structure

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2D Structure of 16-Hydroxytriptolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9548 95.48%
Caco-2 - 0.5538 55.38%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7740 77.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9019 90.19%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior + 0.8180 81.80%
P-glycoprotein inhibitior - 0.7872 78.72%
P-glycoprotein substrate - 0.5646 56.46%
CYP3A4 substrate + 0.6549 65.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8694 86.94%
CYP3A4 inhibition - 0.8854 88.54%
CYP2C9 inhibition - 0.8796 87.96%
CYP2C19 inhibition - 0.8898 88.98%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.7948 79.48%
CYP2C8 inhibition - 0.7138 71.38%
CYP inhibitory promiscuity - 0.8937 89.37%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Danger 0.5470 54.70%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9550 95.50%
Skin irritation - 0.5246 52.46%
Skin corrosion - 0.9303 93.03%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7115 71.15%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5273 52.73%
skin sensitisation - 0.8795 87.95%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6527 65.27%
Acute Oral Toxicity (c) III 0.4744 47.44%
Estrogen receptor binding + 0.7760 77.60%
Androgen receptor binding + 0.7673 76.73%
Thyroid receptor binding + 0.6714 67.14%
Glucocorticoid receptor binding + 0.7598 75.98%
Aromatase binding + 0.6986 69.86%
PPAR gamma + 0.6362 63.62%
Honey bee toxicity - 0.7263 72.63%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9769 97.69%

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 96.48% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.07% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 94.23% 97.79%
CHEMBL2581 P07339 Cathepsin D 94.17% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.27% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.71% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.41% 95.56%
CHEMBL299 P17252 Protein kinase C alpha 90.18% 98.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.06% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.54% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 88.02% 90.17%
CHEMBL226 P30542 Adenosine A1 receptor 87.54% 95.93%
CHEMBL1937 Q92769 Histone deacetylase 2 86.27% 94.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.00% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.76% 89.00%
CHEMBL268 P43235 Cathepsin K 83.70% 96.85%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.20% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.19% 100.00%
CHEMBL5555 O00767 Acyl-CoA desaturase 82.94% 97.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.79% 96.61%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.03% 99.23%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.95% 96.77%

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.
Tripterygium wilfordii

Cross-Links

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PubChem 126556
LOTUS LTS0002881
wikiData Q72482113