Seiricardine B

Details

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Internal ID 880a11d8-9171-449f-925b-c2d9628ee3f3
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name [(4R,7S,8R,11R)-1,3,7,11-tetramethyl-2-oxatricyclo[5.3.1.04,8]undecan-3-yl]methanol
SMILES (Canonical) CC1C2(CCC3C2CCC1(OC3(C)CO)C)C
SMILES (Isomeric) C[C@@H]1[C@]2(CC[C@@H]3[C@H]2CCC1(OC3(C)CO)C)C
InChI InChI=1S/C15H26O2/c1-10-13(2)7-5-12-11(13)6-8-14(10,3)17-15(12,4)9-16/h10-12,16H,5-9H2,1-4H3/t10-,11-,12-,13-,14?,15?/m1/s1
InChI Key KSWAXHCUYHGSQZ-SNNRFPGISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Seiricardine B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9811 98.11%
Caco-2 + 0.7299 72.99%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5501 55.01%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9138 91.38%
OATP1B3 inhibitior + 0.9372 93.72%
MATE1 inhibitior - 0.8812 88.12%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9337 93.37%
P-glycoprotein inhibitior - 0.9343 93.43%
P-glycoprotein substrate - 0.9382 93.82%
CYP3A4 substrate + 0.5727 57.27%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7293 72.93%
CYP3A4 inhibition - 0.7963 79.63%
CYP2C9 inhibition - 0.6964 69.64%
CYP2C19 inhibition - 0.7831 78.31%
CYP2D6 inhibition - 0.9452 94.52%
CYP1A2 inhibition - 0.7021 70.21%
CYP2C8 inhibition - 0.8541 85.41%
CYP inhibitory promiscuity - 0.8540 85.40%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6431 64.31%
Eye corrosion - 0.9536 95.36%
Eye irritation + 0.6361 63.61%
Skin irritation - 0.6642 66.42%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.7870 78.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5898 58.98%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5191 51.91%
skin sensitisation - 0.6361 63.61%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7491 74.91%
Acute Oral Toxicity (c) III 0.7021 70.21%
Estrogen receptor binding + 0.5590 55.90%
Androgen receptor binding + 0.5524 55.24%
Thyroid receptor binding - 0.5500 55.00%
Glucocorticoid receptor binding - 0.6832 68.32%
Aromatase binding - 0.5477 54.77%
PPAR gamma - 0.7688 76.88%
Honey bee toxicity - 0.8991 89.91%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.4019 40.19%

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 95.75% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.24% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.05% 91.11%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 88.53% 89.05%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.10% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.98% 100.00%
CHEMBL233 P35372 Mu opioid receptor 85.16% 97.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.92% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.46% 82.69%
CHEMBL237 P41145 Kappa opioid receptor 83.36% 98.10%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.24% 95.50%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 81.22% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139586574
LOTUS LTS0232896
wikiData Q77509427