Natural Product (NP) Details
| General Information of the NP (ID: NP0310) | |||||
|---|---|---|---|---|---|
| Name |
Succinic acids
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| Species Origin | Pinus ... | Click to Show/Hide | |||
| Pinus | |||||
| Disease | Uterine cancer [ICD-11: 2C76] | Investigative | [1] | ||
| ADMET Property |
Absporption
Caco-2 Permeability
-4.988
MDCK Permeability
-4.785
PAMPA
+++
HIA
- - -
Distribution
VDss
-0.253
PPB
42.5%
BBB
- -
Metabolism
CYP1A2 inhibitor
- - -
CYP1A2 substrate
- - -
CYP2C19 inhibitor
- - -
CYP2C19 substrate
- - -
CYP2C9 inhibitor
- - -
CYP2C9 substrate
+++
CYP2D6 inhibitor
- - -
CYP2D6 substrate
- - -
CYP3A4 inhibitor
- - -
CYP3A4 substrate
- - -
CYP2B6 inhibitor
- - -
CYP2B6 substrate
- - -
CYP2C8 inhibitor
- - -
HLM Stability
- - -
Excretion
CLplasma
3.644
T1/2
1.637
Toxicity
DILI
- -
Rat Oral Acute Toxicity
- -
FDAMDD
- - -
Respiratory
+
Human Hepatotoxicity
-
Ototoxicity
-
Drug-induced Nephrotoxicity
-
Drug-induced Neurotoxicity
- - -
Hematotoxicity
+
Genotoxicity
- -
Tips: 1. For the classification endpoints, the prediction probability values are transformed into six symbols: 0-0.1 (- - -), 0.1-0.3 (- -), 0.3-0.5 (-), 0.5-0.7 (+), 0.7-0.9 (++), and 0.9-1.0 (+++).
2. Additionally, the corresponding relationships of the three labels are as follows: excellent; medium; poor.
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| Herb ID | |||||
| SymMap ID | |||||
| TCMSP ID | |||||
| Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally | ||||||
|---|---|---|---|---|---|---|
| α. A List of Drug(s) Whose Efficacy can be Enhanced by This NP | ||||||
| Trimetazidine | Angina pectoris | Click to Show/Hide the Molecular Data of This Drug | ||||
| Achieving Therapeutic Synergy | Click to Show/Hide | |||||
| Representative Experiment Reporting the Effect of This Combination | [2] | |||||
| Detail(s) |
Combination Info
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| In-vivo Model | The study was carried out on 40 male Wistar rats (230-250 g). | |||||
| Experimental
Result(s) |
A mixture of mitochondrial substrates of succinic and malic acids more effectively than antihypoxant trimetazidine prevented functional and metabolic disorders in rat myocardium during acute ischemia. | |||||