Kalmanol
Kalmanol is a kalmane-type diterpenoid found in Rhododendri Mollis Flos and the leaves of Schinus terebinthifolius. Kalmanol is a state-dependent inhibitor of NaV1.4 channels, and upon binding to inactivated channels, it shifts the fast inactivation curve toward hyperpolarized potentials. Kalmanol exhibits analgesic activity and is used in pain-related research.
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- CAS No.: 118997-92-5
- 화학식: C20H34O6
- 분자량:370.48
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
제품 설명
IC50 & Target
[1]|
hNav1.4 |
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| CHO | IC50 |
199.3 μM
|
Inhibitory effect on human voltage-gated sodium channel NaV1.4 in resting state expressed in CHO cells measured by electrophysiological recordings.
Inhibitory effect on human voltage-gated sodium channel NaV1.4 in resting state expressed in CHO cells measured by electrophysiological recordings.
|
39082673 |
| CHO | IC50 |
19.6 μM
|
Inhibitory effect on human voltage-gated sodium channel NaV1.4 in half-inactivated state expressed in CHO cells measured by electrophysiological recordings.
Inhibitory effect on human voltage-gated sodium channel NaV1.4 in half-inactivated state expressed in CHO cells measured by electrophysiological recordings.
|
39082673 |
In Vitro
Kalmanol (compound 5) (0.025 mmol; 10 h) undergoes chemical transformation under acid-promoted conditions using PPTS in t-BuOH to yield Seco-rhodomollone, Rhodomollein XXIV, and Rhodomollein XXIII[2].
Kalmanol is a state-dependent inhibitor of human NaV1.4 channels expressed in CHO cells, with IC50 values of 199.3 μM and 19.6 μM for the resting and half-inactivated states, respectively; it shifts the voltage dependence of fast inactivation of NaV1.4 by approximately 17 mV toward hyperpolarized potentials[4].
Kalmanol exhibits strong binding affinity with Saccharomyces cerevisiae α-glucosidase (MAL32), inducible nitric oxide synthase (iNOS), and antioxidant pathway-related proteins 2CDU and 3RP8 in molecular docking simulations[5].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 118997-92-5
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분자량 370.48
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화학식 C20H34O6
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SMILES
O[C@@]12[C@@]3([H])[C@](CC[C@@]3([H])[C@](O)(C2)C)([H])[C@@](O)([C@@]4([H])[C@]([C@@H](C1)O)(C(C)([C@H](C4)O)C)O)C
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Structure Classification
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Initial Source
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)