Glanduliferol

Details

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Internal ID 0f03b910-4635-430e-899c-e181cd64e646
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Chamigranes
IUPAC Name 4-bromo-10-chloro-1,5,5,9-tetramethylspiro[5.5]undec-1-en-9-ol
SMILES (Canonical) CC1=CCC(C(C12CCC(C(C2)Cl)(C)O)(C)C)Br
SMILES (Isomeric) CC1=CCC(C(C12CCC(C(C2)Cl)(C)O)(C)C)Br
InChI InChI=1S/C15H24BrClO/c1-10-5-6-11(16)13(2,3)15(10)8-7-14(4,18)12(17)9-15/h5,11-12,18H,6-9H2,1-4H3
InChI Key XTJRMMKSWBOFCC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24BrClO
Molecular Weight 335.71 g/mol
Exact Mass 334.06991 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.65
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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54278-86-3
GLANDULIFEROL
DTXSID80330897
NSC-329496

2D Structure

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2D Structure of Glanduliferol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7250 72.50%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5111 51.11%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9116 91.16%
OATP1B3 inhibitior + 0.9189 91.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9369 93.69%
P-glycoprotein substrate - 0.9233 92.33%
CYP3A4 substrate + 0.5786 57.86%
CYP2C9 substrate - 0.5939 59.39%
CYP2D6 substrate - 0.8017 80.17%
CYP3A4 inhibition - 0.8000 80.00%
CYP2C9 inhibition - 0.7270 72.70%
CYP2C19 inhibition - 0.8228 82.28%
CYP2D6 inhibition - 0.9140 91.40%
CYP1A2 inhibition - 0.9048 90.48%
CYP2C8 inhibition - 0.8844 88.44%
CYP inhibitory promiscuity - 0.8241 82.41%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8472 84.72%
Carcinogenicity (trinary) Non-required 0.6000 60.00%
Eye corrosion - 0.9792 97.92%
Eye irritation - 0.9196 91.96%
Skin irritation + 0.5144 51.44%
Skin corrosion - 0.9310 93.10%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5894 58.94%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6556 65.56%
skin sensitisation + 0.5656 56.56%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5744 57.44%
Acute Oral Toxicity (c) III 0.6306 63.06%
Estrogen receptor binding - 0.6556 65.56%
Androgen receptor binding - 0.5990 59.90%
Thyroid receptor binding - 0.5138 51.38%
Glucocorticoid receptor binding + 0.6195 61.95%
Aromatase binding - 0.5698 56.98%
PPAR gamma - 0.6561 65.61%
Honey bee toxicity - 0.7917 79.17%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9952 99.52%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.33% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.26% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.92% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.56% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.04% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.81% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.93% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.44% 94.45%

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 433418
LOTUS LTS0269742
wikiData Q82095577