(1R,2R,4aR,4bS,6aS,10aR,10bR,12aS)-1-(3-hydroxypropyl)-4b,6a,9,9,10b,12a-hexamethyl-2-prop-1-en-2-yl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysen-2-ol

Details

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Internal ID f6051f95-aff3-49db-9636-379d8cf98a97
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name (1R,2R,4aR,4bS,6aS,10aR,10bR,12aS)-1-(3-hydroxypropyl)-4b,6a,9,9,10b,12a-hexamethyl-2-prop-1-en-2-yl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysen-2-ol
SMILES (Canonical) CC(=C)C1(CCC2C(C1CCCO)(CCC3(C2(CCC4(C3CC(CC4)(C)C)C)C)C)C)O
SMILES (Isomeric) CC(=C)[C@]1(CC[C@@H]2[C@@]([C@H]1CCCO)(CC[C@]3([C@]2(CC[C@]4([C@H]3CC(CC4)(C)C)C)C)C)C)O
InChI InChI=1S/C30H52O2/c1-21(2)30(32)12-11-22-27(6,23(30)10-9-19-31)16-18-29(8)24-20-25(3,4)13-14-26(24,5)15-17-28(22,29)7/h22-24,31-32H,1,9-20H2,2-8H3/t22-,23-,24-,26+,27+,28+,29-,30+/m1/s1
InChI Key MWXHPTNZHHMATE-MSNPTKHSSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H52O2
Molecular Weight 444.70 g/mol
Exact Mass 444.396730897 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 8.90
Atomic LogP (AlogP) 7.53
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,4aR,4bS,6aS,10aR,10bR,12aS)-1-(3-hydroxypropyl)-4b,6a,9,9,10b,12a-hexamethyl-2-prop-1-en-2-yl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysen-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 - 0.5185 51.85%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5237 52.37%
OATP2B1 inhibitior - 0.7208 72.08%
OATP1B1 inhibitior + 0.9062 90.62%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6385 63.85%
BSEP inhibitior + 0.7285 72.85%
P-glycoprotein inhibitior - 0.7551 75.51%
P-glycoprotein substrate - 0.6535 65.35%
CYP3A4 substrate + 0.6504 65.04%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7775 77.75%
CYP3A4 inhibition - 0.7009 70.09%
CYP2C9 inhibition - 0.8817 88.17%
CYP2C19 inhibition - 0.8214 82.14%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.8602 86.02%
CYP2C8 inhibition - 0.6180 61.80%
CYP inhibitory promiscuity - 0.7038 70.38%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6881 68.81%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.8641 86.41%
Skin irritation - 0.6634 66.34%
Skin corrosion - 0.9650 96.50%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4913 49.13%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7098 70.98%
skin sensitisation - 0.5726 57.26%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.6007 60.07%
Acute Oral Toxicity (c) III 0.8312 83.12%
Estrogen receptor binding + 0.8120 81.20%
Androgen receptor binding + 0.6448 64.48%
Thyroid receptor binding + 0.5371 53.71%
Glucocorticoid receptor binding + 0.7376 73.76%
Aromatase binding + 0.7350 73.50%
PPAR gamma + 0.5381 53.81%
Honey bee toxicity - 0.8411 84.11%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9826 98.26%

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 96.27% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.00% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.63% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.38% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.14% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.92% 92.94%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 87.91% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.88% 100.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.64% 95.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.63% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 86.54% 95.38%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.19% 89.05%
CHEMBL2581 P07339 Cathepsin D 86.00% 98.95%
CHEMBL237 P41145 Kappa opioid receptor 85.60% 98.10%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.56% 91.03%
CHEMBL221 P23219 Cyclooxygenase-1 85.17% 90.17%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.68% 92.88%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.45% 92.86%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.88% 95.89%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.85% 91.24%
CHEMBL1951 P21397 Monoamine oxidase A 81.96% 91.49%
CHEMBL233 P35372 Mu opioid receptor 81.80% 97.93%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.58% 96.38%
CHEMBL1937 Q92769 Histone deacetylase 2 81.35% 94.75%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.06% 93.00%

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.
Dischidia formosana
Euphorbia royleana

Cross-Links

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PubChem 102486662
NPASS NPC151844
LOTUS LTS0148945
wikiData Q105173844