Isorotundene

Details

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Internal ID 6146ce2d-760c-4bb8-b02a-c13218cf7cce
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Rotundane sesquiterpenoids
IUPAC Name (2R,5S,6S,8R)-1,5-dimethyl-9-methylidenetricyclo[6.2.2.02,6]dodecane
SMILES (Canonical) CC1CCC2C1CC3CCC2(CC3=C)C
SMILES (Isomeric) C[C@H]1CC[C@@H]2[C@H]1C[C@H]3CCC2(CC3=C)C
InChI InChI=1S/C15H24/c1-10-4-5-14-13(10)8-12-6-7-15(14,3)9-11(12)2/h10,12-14H,2,4-9H2,1,3H3/t10-,12+,13-,14+,15?/m0/s1
InChI Key NPHFULIVCUBDDN-KNDSXMFQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.42
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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NPHFULIVCUBDDN-XFZHLKPQSA-N
Q67879964

2D Structure

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2D Structure of Isorotundene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.8590 85.90%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.8430 84.30%
OATP2B1 inhibitior - 0.8455 84.55%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9346 93.46%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9168 91.68%
P-glycoprotein inhibitior - 0.9219 92.19%
P-glycoprotein substrate - 0.7533 75.33%
CYP3A4 substrate + 0.5706 57.06%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.7523 75.23%
CYP3A4 inhibition - 0.8522 85.22%
CYP2C9 inhibition - 0.8169 81.69%
CYP2C19 inhibition - 0.7636 76.36%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.7197 71.97%
CYP2C8 inhibition - 0.6262 62.62%
CYP inhibitory promiscuity - 0.7790 77.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4544 45.44%
Eye corrosion - 0.8842 88.42%
Eye irritation + 0.8147 81.47%
Skin irritation + 0.5182 51.82%
Skin corrosion - 0.9803 98.03%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4247 42.47%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5246 52.46%
skin sensitisation + 0.8502 85.02%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6479 64.79%
Acute Oral Toxicity (c) III 0.8413 84.13%
Estrogen receptor binding - 0.6919 69.19%
Androgen receptor binding + 0.6399 63.99%
Thyroid receptor binding - 0.7381 73.81%
Glucocorticoid receptor binding - 0.6249 62.49%
Aromatase binding - 0.6866 68.66%
PPAR gamma - 0.8237 82.37%
Honey bee toxicity - 0.7328 73.28%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.8200 82.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.41% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 95.39% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.18% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.26% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 90.31% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.79% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.40% 100.00%

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.
Cyperus rotundus
Piper obliquum

Cross-Links

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PubChem 91753591
NPASS NPC99655
LOTUS LTS0069458
wikiData Q105304343