4,4,6a,6b,8a,9,9,14b-Octamethyl-1,2,3,4a,5,7,8,10,11,12,12a,13,14,14a-tetradecahydropicen-3-ol

Details

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Internal ID 1631a2f4-37be-48ea-b563-e987390c4501
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name 4,4,6a,6b,8a,9,9,14b-octamethyl-1,2,3,4a,5,7,8,10,11,12,12a,13,14,14a-tetradecahydropicen-3-ol
SMILES (Canonical) CC1(CCCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C)C)C)C
SMILES (Isomeric) CC1(CCCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C)C)C)C
InChI InChI=1S/C30H50O/c1-25(2)15-9-10-23-29(25,7)19-18-28(6)21-11-12-22-26(3,4)24(31)14-16-27(22,5)20(21)13-17-30(23,28)8/h11,20,22-24,31H,9-10,12-19H2,1-8H3
InChI Key HGKGZBAXPIRVLR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O
Molecular Weight 426.70 g/mol
Exact Mass 426.386166214 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 9.20
Atomic LogP (AlogP) 8.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,4,6a,6b,8a,9,9,14b-Octamethyl-1,2,3,4a,5,7,8,10,11,12,12a,13,14,14a-tetradecahydropicen-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6804 68.04%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5374 53.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9225 92.25%
OATP1B3 inhibitior + 0.9680 96.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8063 80.63%
P-glycoprotein inhibitior - 0.8160 81.60%
P-glycoprotein substrate - 0.8618 86.18%
CYP3A4 substrate + 0.6368 63.68%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.8699 86.99%
CYP2C9 inhibition - 0.7983 79.83%
CYP2C19 inhibition - 0.6636 66.36%
CYP2D6 inhibition - 0.9399 93.99%
CYP1A2 inhibition - 0.8575 85.75%
CYP2C8 inhibition - 0.7451 74.51%
CYP inhibitory promiscuity - 0.7882 78.82%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5745 57.45%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9216 92.16%
Skin irritation + 0.6645 66.45%
Skin corrosion - 0.9471 94.71%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7619 76.19%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation + 0.6420 64.20%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7684 76.84%
Acute Oral Toxicity (c) III 0.8299 82.99%
Estrogen receptor binding + 0.8283 82.83%
Androgen receptor binding + 0.7009 70.09%
Thyroid receptor binding + 0.7211 72.11%
Glucocorticoid receptor binding + 0.8480 84.80%
Aromatase binding + 0.6529 65.29%
PPAR gamma + 0.5957 59.57%
Honey bee toxicity - 0.8827 88.27%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9875 98.75%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.58% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.96% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.12% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.63% 100.00%
CHEMBL2581 P07339 Cathepsin D 87.96% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.51% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.10% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.89% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.72% 96.77%

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.
Picris hieracioides
Swertia chirata

Cross-Links

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PubChem 73825239
LOTUS LTS0176635
wikiData Q105027817