Sandaracopimaradien-1alpha-ol

Details

Top
Internal ID 9a0378a0-6003-41c0-bdbb-c55eee9c1bc5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name (1S,4aR,4bS,7R,10aR)-7-ethenyl-1,4a,4b,7,10a-pentamethyl-3,4,5,6,9,10-hexahydro-2H-phenanthren-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H34O/c1-7-17(2)13-14-18(3)16(15-17)9-12-20(5)19(18,4)10-8-11-21(20,6)22/h7,15,22H,1,8-14H2,2-6H3/t17-,18-,19+,20+,21-/m0/s1
InChI Key SUEJYRZPHFMIGX-AFDCHOCNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H34O
Molecular Weight 302.50 g/mol
Exact Mass 302.260965704 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.65
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
CHEMBL450422

2D Structure

Top
2D Structure of Sandaracopimaradien-1alpha-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.8535 85.35%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5237 52.37%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.8736 87.36%
OATP1B3 inhibitior + 0.9155 91.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.5859 58.59%
P-glycoprotein inhibitior - 0.9150 91.50%
P-glycoprotein substrate - 0.8810 88.10%
CYP3A4 substrate + 0.5413 54.13%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7424 74.24%
CYP3A4 inhibition - 0.7847 78.47%
CYP2C9 inhibition - 0.7275 72.75%
CYP2C19 inhibition - 0.5964 59.64%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.8085 80.85%
CYP2C8 inhibition - 0.7513 75.13%
CYP inhibitory promiscuity - 0.8476 84.76%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5504 55.04%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.7767 77.67%
Skin irritation + 0.6376 63.76%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.6854 68.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7577 75.77%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6981 69.81%
skin sensitisation + 0.5496 54.96%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8335 83.35%
Acute Oral Toxicity (c) III 0.8426 84.26%
Estrogen receptor binding - 0.6328 63.28%
Androgen receptor binding + 0.7022 70.22%
Thyroid receptor binding + 0.6042 60.42%
Glucocorticoid receptor binding + 0.5479 54.79%
Aromatase binding + 0.6204 62.04%
PPAR gamma - 0.5673 56.73%
Honey bee toxicity - 0.9036 90.36%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9917 99.17%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.21% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.89% 95.56%
CHEMBL1977 P11473 Vitamin D receptor 85.88% 99.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.58% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.45% 98.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.47% 91.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.25% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.33% 86.33%

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.
Kaempferia marginata

Cross-Links

Top
PubChem 44566514
LOTUS LTS0189569
wikiData Q105260852