10,13-Dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

Details

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Internal ID 44b161ad-28c3-4e30-afbb-f6533a9dcd80
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 10,13-dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H48O6/c1-25(16-31)10-12-30(24(35)36)13-11-28(4)18(19(30)15-25)14-20(33)23-26(2)8-7-22(34)27(3,17-32)21(26)6-9-29(23,28)5/h14,19-23,31-34H,6-13,15-17H2,1-5H3,(H,35,36)
InChI Key XZHBPKIHVVAKTG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O6
Molecular Weight 504.70 g/mol
Exact Mass 504.34508925 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10,13-Dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9731 97.31%
Caco-2 - 0.6434 64.34%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7913 79.13%
OATP2B1 inhibitior - 0.5747 57.47%
OATP1B1 inhibitior + 0.8363 83.63%
OATP1B3 inhibitior - 0.4026 40.26%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5602 56.02%
BSEP inhibitior + 0.8612 86.12%
P-glycoprotein inhibitior - 0.7801 78.01%
P-glycoprotein substrate - 0.6964 69.64%
CYP3A4 substrate + 0.6699 66.99%
CYP2C9 substrate - 0.6653 66.53%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8858 88.58%
CYP2C9 inhibition - 0.9175 91.75%
CYP2C19 inhibition - 0.9087 90.87%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition - 0.9089 90.89%
CYP2C8 inhibition - 0.6144 61.44%
CYP inhibitory promiscuity - 0.9354 93.54%
UGT catelyzed - 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6769 67.69%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.9262 92.62%
Skin irritation - 0.5370 53.70%
Skin corrosion - 0.9648 96.48%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4183 41.83%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.7309 73.09%
skin sensitisation - 0.8825 88.25%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.6569 65.69%
Acute Oral Toxicity (c) III 0.7827 78.27%
Estrogen receptor binding + 0.7803 78.03%
Androgen receptor binding + 0.7241 72.41%
Thyroid receptor binding + 0.5416 54.16%
Glucocorticoid receptor binding + 0.7533 75.33%
Aromatase binding + 0.7015 70.15%
PPAR gamma + 0.5632 56.32%
Honey bee toxicity - 0.8558 85.58%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9802 98.02%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 91.39% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.59% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.32% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.18% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.63% 91.11%
CHEMBL5028 O14672 ADAM10 80.34% 97.50%

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 74317396
LOTUS LTS0270908
wikiData Q105344932