Cycloisolongifolene, 8,9-dehydro-9-formyl-

Details

Top
Internal ID 1f2a80ad-891f-485c-a560-1e45e52144d0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 5,5,11,11-tetramethyltetracyclo[6.2.1.01,6.06,10]undec-2-ene-3-carbaldehyde
SMILES (Canonical) CC1(CC(=CC23C14C2CC(C4)C3(C)C)C=O)C
SMILES (Isomeric) CC1(CC(=CC23C14C2CC(C4)C3(C)C)C=O)C
InChI InChI=1S/C16H22O/c1-13(2)6-10(9-17)7-16-12-5-11(14(16,3)4)8-15(12,13)16/h7,9,11-12H,5-6,8H2,1-4H3
InChI Key HXODQHBECCCMFP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H22O
Molecular Weight 230.34 g/mol
Exact Mass 230.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.59
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
HXODQHBECCCMFP-UHFFFAOYSA-N

2D Structure

Top
2D Structure of Cycloisolongifolene, 8,9-dehydro-9-formyl-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8630 86.30%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.5454 54.54%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.8705 87.05%
OATP1B3 inhibitior + 0.9319 93.19%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9449 94.49%
P-glycoprotein inhibitior - 0.9244 92.44%
P-glycoprotein substrate - 0.7787 77.87%
CYP3A4 substrate + 0.5544 55.44%
CYP2C9 substrate - 0.8097 80.97%
CYP2D6 substrate - 0.8123 81.23%
CYP3A4 inhibition - 0.8082 80.82%
CYP2C9 inhibition - 0.6419 64.19%
CYP2C19 inhibition + 0.5368 53.68%
CYP2D6 inhibition - 0.9153 91.53%
CYP1A2 inhibition - 0.7570 75.70%
CYP2C8 inhibition - 0.9189 91.89%
CYP inhibitory promiscuity - 0.5302 53.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.5408 54.08%
Eye corrosion - 0.9524 95.24%
Eye irritation - 0.5882 58.82%
Skin irritation + 0.4939 49.39%
Skin corrosion - 0.9582 95.82%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4243 42.43%
Micronuclear - 0.8926 89.26%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.7557 75.57%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5551 55.51%
Acute Oral Toxicity (c) III 0.7502 75.02%
Estrogen receptor binding - 0.6710 67.10%
Androgen receptor binding + 0.5788 57.88%
Thyroid receptor binding - 0.5689 56.89%
Glucocorticoid receptor binding - 0.7528 75.28%
Aromatase binding - 0.5632 56.32%
PPAR gamma - 0.7467 74.67%
Honey bee toxicity - 0.7386 73.86%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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 93.83% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 91.94% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.35% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.62% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.60% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.18% 82.69%

Plants that contains it

Top
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.
Curcuma longa

Cross-Links

Top
PubChem 615367
NPASS NPC215743