Obtusol(triterpene)

Details

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Internal ID baa4e0c0-a344-4519-9164-72433b35f03a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3S,4aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bR)-6b-(hydroxymethyl)-4,4,6a,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol
SMILES (Canonical) CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)CO)C
SMILES (Isomeric) C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)C)[C@@H]2[C@H]1C)CO)C
InChI InChI=1S/C30H50O2/c1-19-10-13-27(5)16-17-30(18-31)21(25(27)20(19)2)8-9-23-28(6)14-12-24(32)26(3,4)22(28)11-15-29(23,30)7/h8,19-20,22-25,31-32H,9-18H2,1-7H3/t19-,20+,22+,23-,24+,25+,27-,28+,29-,30+/m1/s1
InChI Key MJYXNLJVQSSJFM-SSRSPWJUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O2
Molecular Weight 442.70 g/mol
Exact Mass 442.381080833 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 7.60
Atomic LogP (AlogP) 7.00
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Obtusol(triterpene)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.6138 61.38%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6394 63.94%
OATP2B1 inhibitior - 0.7241 72.41%
OATP1B1 inhibitior + 0.9287 92.87%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5635 56.35%
BSEP inhibitior + 0.8263 82.63%
P-glycoprotein inhibitior - 0.8351 83.51%
P-glycoprotein substrate - 0.7789 77.89%
CYP3A4 substrate + 0.6637 66.37%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate - 0.7222 72.22%
CYP3A4 inhibition - 0.8016 80.16%
CYP2C9 inhibition - 0.8893 88.93%
CYP2C19 inhibition - 0.8457 84.57%
CYP2D6 inhibition - 0.9156 91.56%
CYP1A2 inhibition - 0.8632 86.32%
CYP2C8 inhibition - 0.5651 56.51%
CYP inhibitory promiscuity - 0.6829 68.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6559 65.59%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9517 95.17%
Skin irritation - 0.6560 65.60%
Skin corrosion - 0.9692 96.92%
Ames mutagenesis - 0.8323 83.23%
Human Ether-a-go-go-Related Gene inhibition + 0.6789 67.89%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6976 69.76%
skin sensitisation - 0.6103 61.03%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8728 87.28%
Acute Oral Toxicity (c) III 0.8142 81.42%
Estrogen receptor binding + 0.8078 80.78%
Androgen receptor binding + 0.7257 72.57%
Thyroid receptor binding + 0.6543 65.43%
Glucocorticoid receptor binding + 0.8558 85.58%
Aromatase binding + 0.7136 71.36%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8312 83.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9677 96.77%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.38% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.61% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.37% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.96% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.33% 93.99%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.55% 82.69%
CHEMBL2581 P07339 Cathepsin D 88.11% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.60% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.53% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 86.67% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.83% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.24% 94.45%

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.
Plumeria obtusa
Swertia hickinii

Cross-Links

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PubChem 15895316
NPASS NPC98102
LOTUS LTS0250342
wikiData Q105298818