Horhammerinine

Details

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Internal ID 727e0fc8-58c5-4a25-8422-55e6e26cd90e
Taxonomy Alkaloids and derivatives > Aspidospermatan-type alkaloids
IUPAC Name methyl 12-(1-hydroxyethyl)-5-methoxy-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2(7),3,5,9-tetraene-10-carboxylate
SMILES (Canonical) CC(C12CC(=C3C4(C1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC)C(=O)OC)O
SMILES (Isomeric) CC(C12CC(=C3C4(C1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC)C(=O)OC)O
InChI InChI=1S/C22H26N2O5/c1-11(25)22-9-13(19(26)28-3)17-21(14-5-4-12(27-2)8-15(14)23-17)6-7-24(20(21)22)10-16-18(22)29-16/h4-5,8,11,16,18,20,23,25H,6-7,9-10H2,1-3H3
InChI Key JHLKAIJXPRFWJH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26N2O5
Molecular Weight 398.50 g/mol
Exact Mass 398.18417193 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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NSC109534
NSC-109534

2D Structure

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2D Structure of Horhammerinine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8866 88.66%
Caco-2 + 0.6935 69.35%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6213 62.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9064 90.64%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8427 84.27%
P-glycoprotein inhibitior - 0.6316 63.16%
P-glycoprotein substrate + 0.7207 72.07%
CYP3A4 substrate + 0.7048 70.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8010 80.10%
CYP3A4 inhibition - 0.9515 95.15%
CYP2C9 inhibition - 0.8267 82.67%
CYP2C19 inhibition - 0.8341 83.41%
CYP2D6 inhibition - 0.8155 81.55%
CYP1A2 inhibition - 0.7636 76.36%
CYP2C8 inhibition - 0.6069 60.69%
CYP inhibitory promiscuity - 0.8797 87.97%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4871 48.71%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.9767 97.67%
Skin irritation - 0.7665 76.65%
Skin corrosion - 0.9262 92.62%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6784 67.84%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5342 53.42%
skin sensitisation - 0.8238 82.38%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.6536 65.36%
Acute Oral Toxicity (c) III 0.5204 52.04%
Estrogen receptor binding + 0.6969 69.69%
Androgen receptor binding + 0.7121 71.21%
Thyroid receptor binding + 0.5922 59.22%
Glucocorticoid receptor binding + 0.7241 72.41%
Aromatase binding + 0.7503 75.03%
PPAR gamma + 0.6568 65.68%
Honey bee toxicity - 0.8907 89.07%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9455 94.55%

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 99.45% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.09% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.96% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.66% 94.45%
CHEMBL4208 P20618 Proteasome component C5 96.21% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 94.92% 90.71%
CHEMBL2581 P07339 Cathepsin D 90.62% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 90.42% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.34% 95.89%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.79% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.76% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.28% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 85.04% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.00% 97.09%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.14% 91.03%
CHEMBL2535 P11166 Glucose transporter 83.82% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.39% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.19% 94.00%
CHEMBL240 Q12809 HERG 82.19% 89.76%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.16% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.67% 86.33%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 81.49% 85.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.42% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.19% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.93% 99.15%
CHEMBL4581 P52732 Kinesin-like protein 1 80.85% 93.18%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 80.69% 91.65%
CHEMBL5028 O14672 ADAM10 80.35% 97.50%

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.
Catharanthus roseus

Cross-Links

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PubChem 269014
LOTUS LTS0163785
wikiData Q104253039