CID 162862341

Details

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Internal ID 9947f16b-b031-4546-8d90-a8ed743bbe04
Taxonomy Alkaloids and derivatives > Harmala alkaloids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H35N3O3/c1-32-13-7-17-14-23(33)26(35-3)25-24(17)22(32)16-28(25)8-10-29(11-9-28)27-19(6-12-30-29)20-15-18(34-2)4-5-21(20)31-27/h4-5,14-15,22,30-31,33H,6-13,16H2,1-3H3
InChI Key BUGROTGOGCYEDH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H35N3O3
Molecular Weight 473.60 g/mol
Exact Mass 473.26784199 g/mol
Topological Polar Surface Area (TPSA) 69.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162862341

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9664 96.64%
Caco-2 - 0.6489 64.89%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Lysosomes 0.5244 52.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8899 88.99%
OATP1B3 inhibitior + 0.9365 93.65%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9221 92.21%
P-glycoprotein inhibitior + 0.7718 77.18%
P-glycoprotein substrate + 0.7071 70.71%
CYP3A4 substrate + 0.6943 69.43%
CYP2C9 substrate + 0.6121 61.21%
CYP2D6 substrate + 0.6590 65.90%
CYP3A4 inhibition - 0.8506 85.06%
CYP2C9 inhibition - 0.8621 86.21%
CYP2C19 inhibition - 0.8745 87.45%
CYP2D6 inhibition - 0.5588 55.88%
CYP1A2 inhibition - 0.8201 82.01%
CYP2C8 inhibition - 0.5718 57.18%
CYP inhibitory promiscuity - 0.9189 91.89%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6752 67.52%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.9574 95.74%
Skin irritation - 0.7512 75.12%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7885 78.85%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.6769 67.69%
skin sensitisation - 0.8633 86.33%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.9329 93.29%
Acute Oral Toxicity (c) III 0.5014 50.14%
Estrogen receptor binding + 0.7360 73.60%
Androgen receptor binding + 0.7278 72.78%
Thyroid receptor binding + 0.7018 70.18%
Glucocorticoid receptor binding + 0.6450 64.50%
Aromatase binding + 0.6394 63.94%
PPAR gamma + 0.6997 69.97%
Honey bee toxicity - 0.8088 80.88%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.7338 73.38%

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 99.57% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.98% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.63% 91.49%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 97.17% 93.40%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.11% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.02% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.69% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 94.98% 91.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.89% 97.09%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 94.40% 91.03%
CHEMBL2535 P11166 Glucose transporter 94.25% 98.75%
CHEMBL2056 P21728 Dopamine D1 receptor 93.78% 91.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.68% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.80% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.54% 96.77%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.51% 92.94%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 88.45% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.44% 94.00%
CHEMBL3438 Q05513 Protein kinase C zeta 88.02% 88.48%
CHEMBL4208 P20618 Proteasome component C5 87.39% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.31% 99.15%
CHEMBL233 P35372 Mu opioid receptor 86.90% 97.93%
CHEMBL1907 P15144 Aminopeptidase N 85.35% 93.31%
CHEMBL2581 P07339 Cathepsin D 85.11% 98.95%
CHEMBL3820 P35557 Hexokinase type IV 84.60% 91.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.65% 92.62%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.38% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 80.87% 95.62%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 80.11% 90.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.02% 91.71%

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.
Phoebe grandis

Cross-Links

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PubChem 162862341
LOTUS LTS0031324
wikiData Q104946085