Neocrotocembranal

Details

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Internal ID f466952f-3638-45ca-9222-05aefc39feee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (1E,5E,9E,11E)-5,9-dimethyl-12-propan-2-ylcyclotetradeca-1,5,9,11-tetraene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O/c1-16(2)20-13-11-18(4)8-5-7-17(3)9-6-10-19(15-21)12-14-20/h7,10-11,13,15-16H,5-6,8-9,12,14H2,1-4H3/b17-7+,18-11+,19-10+,20-13+
InChI Key SQMACIRXDFOOLF-SKTYWBPTSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O
Molecular Weight 286.50 g/mol
Exact Mass 286.229665576 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.60
Atomic LogP (AlogP) 5.94
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEMBL509049
(1E,5E,9E,11E)-5,9-dimethyl-12-propan-2-ylcyclotetradeca-1,5,9,11-tetraene-1-carbaldehyde

2D Structure

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2D Structure of Neocrotocembranal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8509 85.09%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.3551 35.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9322 93.22%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8421 84.21%
P-glycoprotein inhibitior - 0.6767 67.67%
P-glycoprotein substrate - 0.9290 92.90%
CYP3A4 substrate - 0.5902 59.02%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8385 83.85%
CYP3A4 inhibition - 0.9611 96.11%
CYP2C9 inhibition - 0.8370 83.70%
CYP2C19 inhibition - 0.8259 82.59%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.6628 66.28%
CYP2C8 inhibition - 0.9453 94.53%
CYP inhibitory promiscuity - 0.7861 78.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5574 55.74%
Eye corrosion + 0.5385 53.85%
Eye irritation - 0.7389 73.89%
Skin irritation + 0.7704 77.04%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7940 79.40%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.8060 80.60%
skin sensitisation + 0.9348 93.48%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.6858 68.58%
Acute Oral Toxicity (c) III 0.6615 66.15%
Estrogen receptor binding - 0.8523 85.23%
Androgen receptor binding - 0.6871 68.71%
Thyroid receptor binding + 0.5710 57.10%
Glucocorticoid receptor binding - 0.5558 55.58%
Aromatase binding - 0.6215 62.15%
PPAR gamma + 0.6158 61.58%
Honey bee toxicity - 0.9031 90.31%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9892 98.92%

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 94.95% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 92.60% 93.40%
CHEMBL3401 O75469 Pregnane X receptor 90.11% 94.73%
CHEMBL2581 P07339 Cathepsin D 89.71% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.26% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.10% 93.56%
CHEMBL4208 P20618 Proteasome component C5 81.06% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.72% 95.50%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.69% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.50% 91.11%

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.
Chrozophora oblongifolia

Cross-Links

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PubChem 10827094
LOTUS LTS0045149
wikiData Q105258093