Terreustoxin G

Details

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Internal ID 62ceb7cd-fedc-405d-bdcb-dece601e1eb3
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (2S,4aR,4bS,5R,6aS,10aS,10bS,12aS)-5-hydroxy-2,4b,7,7,10a,12a-hexamethyl-12-methylidene-5,6a,9,10,10b,11-hexahydro-4aH-naphtho[1,2-h]isochromene-1,4,6,8-tetrone
SMILES (Canonical) CC1C(=O)C2(C(C(=O)O1)C3(C(CC2=C)C4(CCC(=O)C(C4C(=O)C3O)(C)C)C)C)C
SMILES (Isomeric) C[C@H]1C(=O)[C@]2([C@H](C(=O)O1)[C@@]3([C@@H](CC2=C)[C@@]4(CCC(=O)C([C@H]4C(=O)[C@@H]3O)(C)C)C)C)C
InChI InChI=1S/C24H32O6/c1-11-10-13-22(5)9-8-14(25)21(3,4)16(22)15(26)19(28)24(13,7)17-20(29)30-12(2)18(27)23(11,17)6/h12-13,16-17,19,28H,1,8-10H2,2-7H3/t12-,13-,16+,17-,19-,22-,23+,24-/m0/s1
InChI Key OJCUHOMXXINHDN-YMFBSIIISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H32O6
Molecular Weight 416.50 g/mol
Exact Mass 416.21988874 g/mol
Topological Polar Surface Area (TPSA) 97.70 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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(2S,4aR,4bS,5R,6aS,10aS,10bS,12aS)-5-hydroxy-2,4b,7,7,10a,12a-hexamethyl-12-methylidene-5,6a,9,10,10b,11-hexahydro-4aH-naphtho[1,2-h]isochromene-1,4,6,8-tetrone
(2S,4aR,4bS,5R,6aS,10aS,10bS,12aS)-5-hydroxy-2,4b,7,7,10a,12a-hexamethyl-12-methylidene-5,6a,9,10,10b,11-hexahydro-4aH-naphtho(1,2-h)isochromene-1,4,6,8-tetrone
RefChem:188140
CHEBI:227712

2D Structure

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2D Structure of Terreustoxin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9527 95.27%
Caco-2 - 0.6615 66.15%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7789 77.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8331 83.31%
OATP1B3 inhibitior + 0.8573 85.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.9010 90.10%
P-glycoprotein inhibitior - 0.4596 45.96%
P-glycoprotein substrate - 0.6888 68.88%
CYP3A4 substrate + 0.6140 61.40%
CYP2C9 substrate - 0.8217 82.17%
CYP2D6 substrate - 0.8422 84.22%
CYP3A4 inhibition - 0.6383 63.83%
CYP2C9 inhibition - 0.9182 91.82%
CYP2C19 inhibition - 0.8679 86.79%
CYP2D6 inhibition - 0.9369 93.69%
CYP1A2 inhibition - 0.6704 67.04%
CYP2C8 inhibition - 0.7888 78.88%
CYP inhibitory promiscuity - 0.9637 96.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7109 71.09%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.8976 89.76%
Skin irritation + 0.5767 57.67%
Skin corrosion - 0.9158 91.58%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4431 44.31%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.6158 61.58%
skin sensitisation - 0.6378 63.78%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5309 53.09%
Acute Oral Toxicity (c) III 0.7445 74.45%
Estrogen receptor binding + 0.6472 64.72%
Androgen receptor binding + 0.6992 69.92%
Thyroid receptor binding + 0.6487 64.87%
Glucocorticoid receptor binding + 0.7642 76.42%
Aromatase binding + 0.6458 64.58%
PPAR gamma - 0.4879 48.79%
Honey bee toxicity - 0.7987 79.87%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9941 99.41%

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
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.59% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.40% 95.56%
CHEMBL204 P00734 Thrombin 89.35% 96.01%
CHEMBL2581 P07339 Cathepsin D 88.20% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.97% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.37% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.46% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.00% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146682419
LOTUS LTS0104563
wikiData Q105193005