Tetrahydrocucurbitacin I

Details

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Internal ID 022bd55c-ec0e-4d41-bb2c-a930ca1829d3
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cucurbitacins
IUPAC Name 17-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H46O7/c1-25(2,36)12-11-21(33)30(8,37)23-19(32)14-27(5)20-10-9-16-17(13-18(31)24(35)26(16,3)4)29(20,7)22(34)15-28(23,27)6/h9,17-20,23,31-32,36-37H,10-15H2,1-8H3
InChI Key ITMUUFDDBRYVNJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O7
Molecular Weight 518.70 g/mol
Exact Mass 518.32435380 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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NSC112164
NSC-112164

2D Structure

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2D Structure of Tetrahydrocucurbitacin I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 - 0.6122 61.22%
Blood Brain Barrier + 0.9138 91.38%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7952 79.52%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.8651 86.51%
OATP1B3 inhibitior + 0.8759 87.59%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6596 65.96%
BSEP inhibitior + 0.7549 75.49%
P-glycoprotein inhibitior - 0.4587 45.87%
P-glycoprotein substrate - 0.5546 55.46%
CYP3A4 substrate + 0.6751 67.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8029 80.29%
CYP3A4 inhibition - 0.7882 78.82%
CYP2C9 inhibition - 0.8572 85.72%
CYP2C19 inhibition - 0.8174 81.74%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.9401 94.01%
CYP2C8 inhibition + 0.4563 45.63%
CYP inhibitory promiscuity - 0.8614 86.14%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6884 68.84%
Eye corrosion - 0.9934 99.34%
Eye irritation - 0.9269 92.69%
Skin irritation + 0.6621 66.21%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6967 69.67%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5914 59.14%
skin sensitisation - 0.8033 80.33%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.7037 70.37%
Acute Oral Toxicity (c) I 0.6370 63.70%
Estrogen receptor binding + 0.7046 70.46%
Androgen receptor binding + 0.7399 73.99%
Thyroid receptor binding + 0.6647 66.47%
Glucocorticoid receptor binding + 0.8171 81.71%
Aromatase binding + 0.7719 77.19%
PPAR gamma - 0.4942 49.42%
Honey bee toxicity - 0.7791 77.91%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9925 99.25%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.04% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.66% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.98% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.41% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.90% 94.45%
CHEMBL2996 Q05655 Protein kinase C delta 88.31% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.37% 95.56%
CHEMBL4208 P20618 Proteasome component C5 85.02% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.88% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.55% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.54% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.08% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.37% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.14% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.09% 99.23%

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.
Begonia heracleifolia
Bryonia cretica
Cucumis melo
Dendrosicyos socotrana
Trichosanthes tricuspidata

Cross-Links

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PubChem 270059
LOTUS LTS0184921
wikiData Q105120138