The terpenoids are a large and diverse class of naturally occurring organic chemicals, derived from five-carbon isoprene units assembled and modified in thousands of ways. Most are multicyclic structures that differ from one another not only in functional groups but also in their basic carbon skeletons. They can be classified according to the number of isoprene units used: Hemiterpenoids, Monoterpenoids, Sesquiterpenoids, Diterpenoids, Sesterterpenoids, Triterpenoids, Tetraterpenoids. These lipids can be found in all classes of living things, and are the largest group of natural products. Plant terpenoids are used extensively for their aromatic qualities and play a role in traditional herbal remedies. Terpenoids contribute to the scent of eucalyptus, the flavors of cinnamon, cloves, and ginger, the yellow color in sunflowers, and the red color in tomatoes.


Anti-infection >
Arenavirus Bacterial CMV Enterovirus Filovirus Fungal HBV HCV HIV HSV Influenza Virus Parasite Reverse Transcriptase RSV SARS-CoV
Antibody-drug Conjugate >
ADC Cytotoxin ADC Linker Drug-Linker Conjugates for ADC PROTAC-linker Conjugate for PAC
Apoptosis >
Apoptosis Bcl-2 Family c-Myc Caspase DAPK Ferroptosis IAP MDM-2/p53 PKD RIP kinase Survivin Thymidylate Synthase TNF Receptor
Autophagy >
Autophagy LRRK2 ULK Mitophagy
Cell Cycle/DNA Damage >
Antifolate APC ATM/ATR Aurora Kinase Casein Kinase CDK Checkpoint Kinase (Chk) CRISPR/Cas9 Deubiquitinase DNA Alkylator/Crosslinker DNA-PK DNA/RNA Synthesis Eukaryotic Initiation Factor (eIF) G-quadruplex Haspin Kinase HDAC HSP IRE1 Kinesin LIM Kinase (LIMK) Microtubule/Tubulin Mps1 Nucleoside Antimetabolite/Analog p97 PAK PARP PERK Polo-like Kinase (PLK) PPAR RAD51 ROCK Sirtuin SRPK Telomerase TOPK Topoisomerase Wee1
Cytoskeleton >
Arp2/3 Complex Dynamin Gap Junction Protein Integrin Kinesin Microtubule/Tubulin Mps1 Myosin PAK
Epigenetics >
AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain HDAC Histone Acetyltransferase Histone Demethylase Histone Methyltransferase JAK MicroRNA PARP PKC Sirtuin Protein Arginine Deiminase
GPCR/G Protein >
5-HT Receptor Adenosine Receptor Adenylate Cyclase Adiponectin Receptor Adrenergic Receptor Angiotensin Receptor Bombesin Receptor Bradykinin Receptor Cannabinoid Receptor CaSR CCR CGRP Receptor Cholecystokinin Receptor CRFR CXCR Dopamine Receptor EBI2/GPR183 Endothelin Receptor GHSR Glucagon Receptor Glucocorticoid Receptor GNRH Receptor GPCR19 GPR109A GPR119 GPR120 GPR139 GPR40 GPR55 GPR84 Guanylate Cyclase Histamine Receptor Imidazoline Receptor Leukotriene Receptor LPL Receptor mAChR MCHR1 (GPR24) Melatonin Receptor mGluR Motilin Receptor Neurokinin Receptor Neuropeptide Y Receptor Neurotensin Receptor Opioid Receptor Orexin Receptor (OX Receptor) Oxytocin Receptor P2Y Receptor Prostaglandin Receptor Protease-Activated Receptor (PAR) Ras RGS Protein Sigma Receptor Somatostatin Receptor TSH Receptor Urotensin Receptor Vasopressin Receptor Melanocortin Receptor
Immunology/Inflammation >
Aryl Hydrocarbon Receptor CCR Complement System COX CXCR FLAP Histamine Receptor IFNAR Interleukin Related IRAK MyD88 NO Synthase NOD-like Receptor (NLR) PD-1/PD-L1 PGE synthase Salt-inducible Kinase (SIK) SPHK STING Thrombopoietin Receptor Toll-like Receptor (TLR) Arginase
JAK/STAT Signaling >
EGFR JAK Pim STAT
MAPK/ERK Pathway >
ERK JNK KLF MAP3K MAP4K MAPKAPK2 (MK2) MEK Mixed Lineage Kinase MNK p38 MAPK Raf Ribosomal S6 Kinase (RSK)
Membrane Transporter/Ion Channel >
ATP Synthase BCRP Calcium Channel CFTR Chloride Channel CRAC Channel CRM1 EAAT2 GABA Receptor GlyT HCN Channel iGluR Monoamine Transporter Monocarboxylate Transporter Na+/Ca2+ Exchanger Na+/HCO3- Cotransporter Na+/K+ ATPase nAChR NKCC P-glycoprotein P2X Receptor Potassium Channel Proton Pump SGLT Sodium Channel TRP Channel URAT1
Metabolic Enzyme/Protease >
15-PGDH 5 alpha Reductase 5-Lipoxygenase Acetyl-CoA Carboxylase Acyltransferase Adenosine Deaminase Adenosine Kinase Aldehyde Dehydrogenase (ALDH) Aldose Reductase Aminopeptidase Angiotensin-converting Enzyme (ACE) ATGL ATP Citrate Lyase Carbonic Anhydrase Carboxypeptidase Cathepsin CETP COMT Cytochrome P450 Dipeptidyl Peptidase Dopamine β-hydroxylase E1/E2/E3 Enzyme Elastase Enolase FAAH FABP Factor Xa Farnesyl Transferase Fatty Acid Synthase (FAS) FXR Glucokinase GSNOR Gutathione S-transferase HCV Protease Hexokinase HIF/HIF Prolyl-Hydroxylase HIV Integrase HIV Protease HMG-CoA Reductase (HMGCR) HSP Indoleamine 2,3-Dioxygenase (IDO) Isocitrate Dehydrogenase (IDH) Lactate Dehydrogenase LXR MAGL Mineralocorticoid Receptor Mitochondrial Metabolism MMP Nampt NEDD8-activating Enzyme Neprilysin PAI-1 PDHK PGC-1α Phosphatase Phosphodiesterase (PDE) Phospholipase Procollagen C Proteinase Proteasome Pyruvate Kinase RAR/RXR Renin ROR Ser/Thr Protease SGK Stearoyl-CoA Desaturase (SCD) Thrombin Tryptophan Hydroxylase Tyrosinase Xanthine Oxidase
Neuronal Signaling >
5-HT Receptor AChE Adenosine Kinase Amyloid-β Beta-secretase CaMK CGRP Receptor COMT Dopamine Receptor Dopamine Transporter FAAH GABA Receptor GlyT iGluR Imidazoline Receptor mAChR Melatonin Receptor Monoamine Oxidase nAChR Neurokinin Receptor Opioid Receptor Serotonin Transporter γ-secretase
NF-κB >
NF-κB IKK Keap1-Nrf2 MALT1
PI3K/Akt/mTOR >
Akt AMPK ATM/ATR DNA-PK GSK-3 MELK mTOR PDK-1 PI3K PI4K PIKfyve PTEN
PROTAC >
PROTAC E3 Ligase Ligand-Linker Conjugate Ligand for E3 Ligase PROTAC Linker PROTAC-linker Conjugate for PAC
Protein Tyrosine Kinase/RTK >
Ack1 ALK Bcr-Abl BMX Kinase Btk c-Fms c-Kit c-Met/HGFR Discoidin Domain Receptor DYRK EGFR Ephrin Receptor FAK FGFR FLT3 IGF-1R Insulin Receptor IRAK Itk PDGFR PKA Pyk2 ROS Src Syk TAM Receptor Trk Receptor VEGFR
Stem Cell/Wnt >
Casein Kinase ERK Gli GSK-3 Hedgehog Hippo (MST) JAK Notch Oct3/4 PKA Porcupine ROCK sFRP-1 Smo STAT TGF-beta/Smad Wnt YAP β-catenin γ-secretase
TGF-beta/Smad >
TGF-beta/Smad PKC ROCK TGF-β Receptor
Vitamin D Related >
VD/VDR
Others >
Androgen Receptor Aromatase Estrogen Receptor/ERR Progesterone Receptor Thyroid Hormone Receptor Others

Glycyrrhetinic acid

18β-Glycyrrhetinic acid is the major bioactive component of Glycyrrhizae Radix and possesses anti-ulcerative, anti-inflammatory and antiproliferative properties.

  • CAS Number: 471-53-4
  • MF: C30H46O4
  • MW: 470.684
  • Catalog: Cancer
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 588.3±50.0 °C at 760 mmHg
  • Melting Point: 292 - 295ºC
  • Flash Point: 323.7±26.6 °C

Triptophenolide

Triptophenolide is a colorless crystalline plate isolated from ethyl acetate extracts of Tripterygium wilfordii. IC50 value:Target:In vitro: Triptophenolide can remarkably inhibit the delayed type hypersensitivity (DTH) reaction induced by DNCB and BSA; and diminished the peripheral blood ANAE+lymphocytes in rats and micc. Moreover, triptophenolide can dramatically increase the amount of total serum complement and significautly decrcase the serum antibody products (1gG ) of rats and mice. The phagocytosis of perioneal exudate macrophages in mice present double effects in vitro [1].In vivo:

  • CAS Number: 74285-86-2
  • MF: C20H24O3
  • MW: 312.403
  • Catalog: Others
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 490.0±45.0 °C at 760 mmHg
  • Melting Point: 232-233ºC
  • Flash Point: 202.4±21.5 °C

Paclitaxel

Paclitaxel is a potent anticancer medication which can promote microtubule (MT) assembly, inhibit MT depolymerization, and change MT dynamics required for mitosis and cell proliferation.

  • CAS Number: 33069-62-4
  • MF: C47H51NO14
  • MW: 853.906
  • Catalog: ADC Cytotoxin
  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 957.1±65.0 °C at 760 mmHg
  • Melting Point: 213 °C (dec.)(lit.)
  • Flash Point: 532.6±34.3 °C

Cynaropicrin

Cynaropicrin is a sesquiterpene lactone which can inhibit tumor necrosis factor (TNF-α) release with IC50s of 8.24 and 3.18 μM for murine and human macrophage cells, respectively. Cynaropicrin also inhibits the increase of cartilage degradation factor (MMP13) and suppresses NF-κB signaling.

  • CAS Number: 35730-78-0
  • MF: C19H22O6
  • MW: 346.37400
  • Catalog: TNF Receptor
  • Density: 1.28g/cm3
  • Boiling Point: 566.2ºC at 760mmHg
  • Melting Point: N/A
  • Flash Point: 203.8ºC

alpha-Boswellic acid

alpha-Boswellic acid is a natural product.

  • CAS Number: 471-66-9
  • MF: C30H48O3
  • MW: 456.700
  • Catalog: Others
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 552.7±50.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 302.1±26.6 °C

Ursolic Acid

Ursolic acid(Bungeolic acid) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy. IC50 value:Target:in vitro: UA induced phosphorylation of AMP-activated protein kinase alpha (AMPKα) and suppressed the protein expression of DNA methyltransferase 1 (DNMT1) in the dose-dependent manner [1]. The combination of ursolic acid (0.5 μM) and leucine (10 μM) proved to be the most effective in promoting myogenic differentiation. The combination of ursolic acid and leucine significantly increased CK activity than treatment with either agent alone. The level of myosin heavy chain, a myogenic differentiation marker protein, was also enhanced by the combination of ursolic acid and leucine [2]. Ursolic acid efficiently induced apoptosis, possibly via the downregulation of B-cell lymphoma 2 (Bcl-2), the upregulation of Bcl-2-associated X protein and the proteolytic activation of caspase-3. Furthermore, the activation of p38 mitogen-activated protein kinase and c-Jun N-terminal kinase was increased by the administration of ursolic acid. In addition, ursolic acid significantly suppressed the invasive phenotype of the SNU-484 cells and significantly decreased the expression of matrix metalloproteinase (MMP)-2 [3]. ursolic acid (UA) potently induces the apoptosis of gastric cancer SGC-7901 cells. Further mechanistic studies revealed that the ROCK1/PTEN signaling pathway plays a critical role in UA-mediated mitochondrial translocation of cofilin-1 and apoptosis [4].in vivo: UA treatment markedly improved the survival of septic rats, and attenuated CLP-induced lung injury, including reduction of lung wet/dry weight ratio, infiltration of leukocytes and proteins, myeloperoxidase activity, and malondialdehyde content. In addition, UA significantly decreased the serum levels of tumor necrosis factor-α, interleukin-6, and interleukin-1β, inhibited the expression of inducible nitric oxide synthase and cyclooxygenase-2 in the lung, which are involved in the productions of nitric oxide and prostaglandin E2 [5].

  • CAS Number: 77-52-1
  • MF: C30H48O3
  • MW: 456.700
  • Catalog: Apoptosis
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 556.9±50.0 °C at 760 mmHg
  • Melting Point: 292 °C (dec.)(lit.)
  • Flash Point: 304.7±26.6 °C

20-Deoxyingenol

20-Deoxyingenol is a natural compound.

  • CAS Number: 54706-99-9
  • MF: C20H28O4
  • MW: 332.434
  • Catalog: Others
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 470.5±45.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 252.4±25.2 °C

Ginsenoside Rg3

Ginsenoside Rg3 is the main component of Red ginseng. Ginsenoside Rg3 inhibits Na+ and hKv1.4 channel with IC50s of 32.2±4.5 and 32.6±2.2 μM, respectively. Ginsenoside Rg3 also inhibits Aβ levels, NF-κB activity, and COX-2 expression.

  • CAS Number: 14197-60-5
  • MF: C42H72O13
  • MW: 785.013
  • Catalog: COX
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 885.0±65.0 °C at 760 mmHg
  • Melting Point: 315-318°C
  • Flash Point: 489.0±34.3 °C

Parthenolide

Parthenolide is an NF-κB inhibitor, reduces histone deacetylase 1 (HDAC-1) and DNA methyltransferase 1 independent of NF-κB inhibition.

  • CAS Number: 20554-84-1
  • MF: C15H20O3
  • MW: 248.318
  • Catalog: Autophagy
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 394.1±42.0 °C at 760 mmHg
  • Melting Point: 115-116ºC(lit.)
  • Flash Point: 166.3±22.5 °C

Picrotoxin

Picrotoxin is a noncompetitive antagonist of GABAA receptor.

  • CAS Number: 124-87-8
  • MF: C15H18O7.C15H16O6
  • MW: 301.29
  • Catalog: GABA Receptor
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: 203 ℃(lit.)
  • Flash Point: N/A

Curdione

Curdione, one of the major sesquiterpene compounds from Rhizoma Curcumae, has been shown to exhibit multiple bioactive properties.IC50 value: 60–80 μMTarget:In vitro: The study of the influence of curdione on the hemorheological changes in blood stasis model rats and thrombolysis in vitro showed that curdione only possessed thrombolytic effect in dose of 0.235 g·L-1 and 2.35 g·L-1, but has not the notable activity of thrombolysis [1]. The effects of curdione on human platelet aggregation induced by thrombin (0.3 U/ml) were tested in vitro. Curdione preferentially inhibited PAF- and thrombin- induced platelet aggregation in a concentration-dependent manner (IC50: 60–80 μM), whereas much higher concentrations of curdione were required to inhibit platelet aggregation induced by ADP and AA. Curdione also inhibited P-selectin expression in PAF-activated platelets. Moreover, curdione caused an increase in cAMP levels and attenuated intracellular Ca2+ mobilization in PAF-activated platelets. In vivo: Curdione showed significant antithrombotic activity [2].

  • CAS Number: 13657-68-6
  • MF: C15H24O2
  • MW: 236.350
  • Catalog: Others
  • Density: 0.9±0.1 g/cm3
  • Boiling Point: 347.6±42.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 130.4±24.9 °C

Cineole

Eucalyptol is an inhibitor of 5-HT3 receptor ,potassium channel, TNF-α and IL-1β.

  • CAS Number: 470-82-6
  • MF: C10H18O
  • MW: 154.249
  • Catalog: TNF Receptor
  • Density: 0.9±0.1 g/cm3
  • Boiling Point: 174.0±8.0 °C at 760 mmHg
  • Melting Point: 1.5ºC
  • Flash Point: 50.9±15.3 °C

farnesol

Farnesol is a sesquiterpene alcohol that modulates cell-to-cell communication in Candida albicans, and has the activity in inhibiting bacteria.

  • CAS Number: 4602-84-0
  • MF: C15H26O
  • MW: 222.366
  • Catalog: Bacterial
  • Density: 0.9±0.1 g/cm3
  • Boiling Point: 283.4±0.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 96.1±0.0 °C

Ingenol

Ingenol is a PKC activator, with a Ki of 30 μM, with antitumor activity.

  • CAS Number: 30220-46-3
  • MF: C20H28O5
  • MW: 348.433
  • Catalog: Cancer
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 523.8±50.0 °C at 760 mmHg
  • Melting Point: 153 °C
  • Flash Point: 284.7±26.6 °C

Alisol C monoacetate

Alisol C 23-acetate, a natural product extracted from Alisma orientale, can significantly and strongly inhibit DTH response after oral administration.

  • CAS Number: 26575-93-9
  • MF: C32H48O6
  • MW: 528.720
  • Catalog: Cardiovascular Disease
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 624.9±55.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 192.9±25.0 °C

Dodecanoic acid ingenol ester

Dodecanoic acid ingenol ester is a natural compound.

  • CAS Number: 54706-70-6
  • MF: C32H50O7
  • MW: 546.735
  • Catalog: Others
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 655.2±55.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 201.6±25.0 °C

Alismoxide

Alismoxide is a natural product.

  • CAS Number: 87701-68-6
  • MF: C15H26O2
  • MW: 238.366
  • Catalog: Others
  • Density: 1.0±0.1 g/cm3
  • Boiling Point: 343.2±42.0 °C at 760 mmHg
  • Melting Point: 140-142ºC
  • Flash Point: 153.9±22.5 °C

Pristimerin

Pristimerin is a potent and reversible monoacylglycerol lipase (MGL) inhibitor with an IC50 of 93 nM.

  • CAS Number: 1258-84-0
  • MF: C30H40O4
  • MW: 464.636
  • Catalog: Bacterial
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 607.7±55.0 °C at 760 mmHg
  • Melting Point: 219.5°C
  • Flash Point: 195.1±25.0 °C

3-oxo-Olean-12-en-28-oic acid

Oleanolic acid is a triterpenoid, inhibits infection by HIV-1 in in vitro infected PBMC, naturally infected PBMC and monocyte/macrophages with EC50 of 22.7 mM, 24.6 mM and 57.4 mM, respectively. Besides,it has IC50 of 17μM for the production of leukotriene B4 from rat peritoneal leukocytes.IC50:17μM(The production of leukotriene B4 from rat peritoneal leukocytes)[1]IC50:22.7 mM, 24.6 mM and 57.4 mM(in vitro infected PBMC, naturally infected PBMC and monocyte/macrophages by HIV-1, respectively.[2]In vitro: The highest of the four tested doses (100 μM), showed only a slight inhibition approximately, 30%. In contrast, the more powerful effect of oleanonic acid in this system, suggests that it acts through a mechanism related to the inhibition of 5-lipoxygenase, either directly or interfering with some of the mechanisms that participate in the complex activation of this enzyme. Oleanonic acid also acts by reducing prostaglandin synthesis.[1]Oleanolic acid inhibits the HIV-1 replication in all the cellular systems used (EC50 values: 22.7 microM, 24.6 microM and 57.4 microM for in vitro infected PBMC, naturally infected PBMC and M/M, respectively). As regards the mechanism of action, oleanolic acid inhibits in vitro the HIV-1 protease activity.[2]In vivo: Oleanonic acid exerted no activity on the oedema induced by application of ethyl phenylpropiolate after a pre-treatment of 16 h. In the TPA ear oedema test, it showed a non-significant 28% inhibition. However, when assayed on the ear oedema induced by DPP, oleanonic acid reduced the swelling by 40%, an effect similar to that of the standard carbamazepine. In the mouse model of delayed hypersensitivity induced by dinitrofluorobenzene, oleanonic acid was ineffective at both 24 and 96 h, while oleanolic acid reduced non-significantly the oedema at 96 h by 32%.In the TPA model of chronic inflammation induced by multiple applications, oleanonic acid showed a significant effect, with 45% inhibition. In contrast, oleanolic acid was inactive. Both inhibited the neutrophil infiltration measured as myeloperoxidase activity by 84% and 67%, respectively. The inhibition observed for dexamethasone on the swelling and myeloperoxidase activity was around 90%. The histological study of ears treated only with repeated doses of TPA showed an extensive diffusive inflammatory lesion with microabscesses affecting dermis and epidermis. The main infiltrating cells in the skin were neutrophils and epithelial thickness was 6.6±1.0 cells. In the tissues treated only with the solvent acetone, epithelial thickness was 2.1±0.5 and no signs of lesion or leukocyte infiltration were detectable. The multidose treatment with oleanonic acid reduced both the intensity and extension of the damage produced by TPA, as this was localized in the dermis, where the main infiltrating cells were lymphocytes, and where fibrosis was observed. In this case, epithelium thickness was 4.4±0.7 cells. The ears treated with dexamethasone showed minimal inflammatory lesions and sometimes none at all, and the epithelium thickness was 4.3±0.7 cells.The paw oedema induced by bradykinin was significantly reduced (61%) by oleanonic acid, whereas isoprenaline had a slightly lower effect (52%). Both oleanolic and oleanonic acid also reduced the paw oedema induced by phospholipase A2; the latter showing its strongest effect at 60 min, with an 84% inhibition, and maintaining activity at 90 min. Oleanolic acid also had its maximum effect at 60 min, vanishing at 90 min, while the activity of cyproheptadine was uniform along the experiment, ranging 80–90% inhibition .[1]

  • CAS Number: 17990-42-0
  • MF: C30H46O3
  • MW: 454.684
  • Catalog: HIV
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 551.7±50.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 301.5±26.6 °C

Dipsacoside B

Dipsacoside B is a major bioactive saponin, which can be used as a marker.

  • CAS Number: 33289-85-9
  • MF: C53H86O22
  • MW: 1075.237
  • Catalog: Inflammation/Immunology
  • Density: 1.5±0.1 g/cm3
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Betulinaldehyde

Betulinaldehyde(Betunal) belongs to pentacyclic triterpenoids and was reported to exhibit antimicrobial activities against bacteria and fungi, including S. aureus.IC50 value:Target: Betulinaldehyde(Betunal) belongs to pentacyclic triterpenoids that are based on a 30-carbon skeleton comprising four six-membered rings and one five-membered ring. Betulinaldehyde regulates multiple desirable targets which could be further explored in the development of therapeutic agents for the treatment of S. aureus infections [1]. Study compounds α-amyrin [3β-hydroxy-urs-12-en-3-ol (AM)], betulinic acid [3β-hydroxy-20(29)-lupaene-28-oic acid (BA)] and betulinaldehyde [3β-hydroxy-20(29)-lupen-28-al (BE)] belong to pentacyclic triterpenoids and were reported to exhibit antimicrobial activities against bacteria and fungi, including S. aureus. The MIC values of these compounds against a reference strain of methicillin-resistant S. aureus (MRSA) (ATCC 43300) ranged from 64 μg/ml to 512 μg/ml. However, the response mechanisms of S. aureus to these compounds are still poorly understood [2].

  • CAS Number: 13159-28-9
  • MF: C30H48O2
  • MW: 440.701
  • Catalog: Bacterial
  • Density: 1.0±0.1 g/cm3
  • Boiling Point: 513.9±33.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 217.4±18.0 °C

Alisol B 23-acetate

Alisol B 23-acetate, a natural triterpenoid, produces protective effects against EE-induced cholestasis, due to FXR-mediated gene regulation.IC50 Value:Target: Anti-hepatotoxic natural product. In vitro: Alisol-B 23-acetate has an effect on FXR activation in a dose-dependent manner using luciferase reporter assay in HepG2 cells [3].In vivo: In alisol B 23-acetate-treated mice, the changes in transporters and enzymes, as well as ameliorative liver histology were abrogated by FXR antagonist guggulsterone [1]. Alisol B 23-acetate treatment in a dose-dependent manner resulted in protection against hepatotoxicity induced by CCl4via FXR activation. Through FXR activation, alisol B 23-acetate promoted hepatocyte proliferation via an induction in hepatic levels of FoxM1b, Cyclin D1 and Cyclin B1. Alisol B 23-acetate also reduced hepatic bile acids through a decrease in hepatic uptake transporter Ntcp, bile acid synthetic enzymes Cyp7a1, Cyp8b1, and an increase in efflux transporter Bsep, Mrp2 expression. In addition, alisol B 23-acetate induced the expression of STAT3 phosphorylation, and STAT3 target genes Bcl-xl and SOCS3, resulting in decreased hepatocyte apoptosis [2].

  • CAS Number: 26575-95-1
  • MF: C32H50O5
  • MW: 514.736
  • Catalog: Others
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 590.7±50.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 179.9±23.6 °C

Hederacoside C

Hederacoside C is a principal bioactive pharmaceutical ingredient of Hedera helix leaf that can treat respiratory disorders, because of its expectorant, bronchodilator, antibacterial, and bronchospasmolytic effects.

  • CAS Number: 14216-03-6
  • MF: C59H96O26
  • MW: 1221.378
  • Catalog: Infection
  • Density: 1.5±0.1 g/cm3
  • Boiling Point: N/A
  • Melting Point: 222ºC (dec.)(lit.)
  • Flash Point: N/A

Alantolactone

Alantolactone is a selective STAT3 inhibitor, with potent anticancer activity.

  • CAS Number: 546-43-0
  • MF: C15H20O2
  • MW: 232.318
  • Catalog: Cancer
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 275.0±0.0 °C at 760 mmHg
  • Melting Point: 78-79ºC
  • Flash Point: 111.5±18.2 °C

Astragaloside II

Astragaloside II is a natural isolated from Astragalus.IC50 value:Target:In vitro:In vivo: The developed and validated method has been successfully applied to the quantification and pharmacokinetic study of AST II in rats after intravenous and oral administration of AST II. The oral absolute bioavailability (F) of AST II was calculated to be 0.79 ± 0.16% with an elimination half-life (t1/2) value of 1.92 ± 0.30 h, suggesting its poor absorption and/or strong metabolism in vivo [1].

  • CAS Number: 84676-89-1
  • MF: C43H70O15
  • MW: 827.01
  • Catalog: Others
  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 896.9±65.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 265.3±27.8 °C

Betulinic acid

Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties.

  • CAS Number: 472-15-1
  • MF: C30H48O3
  • MW: 456.700
  • Catalog: HIV
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 550.0±33.0 °C at 760 mmHg
  • Melting Point: 295-298 °C (dec.)(lit.)
  • Flash Point: 300.5±21.9 °C

8-O-Acetylshanzhiside methyl ester

8-O-Acetyl shanzhiside methyl ester (ND01) is an iridoid glucoside isolated from the leaves of Lamiophlomis rotata Kudo, a Chinese folk medicinal plant in Xi-zang. 8-O-Acetyl shanzhiside methyl ester could inhibt NF-κB.

  • CAS Number: 57420-46-9
  • MF: C19H28O12
  • MW: 448.418
  • Catalog: Inflammation/Immunology
  • Density: 1.52 g/cm3
  • Boiling Point: 634.2±55.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 220.0±25.0 °C

Atractyloside A

Atractyloside A(126054-77-1) is a natural TCM reference compound.

  • CAS Number: 126054-77-1
  • MF: C21H36O10
  • MW: 448.504
  • Catalog: Others
  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 684.8±55.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 234.1±25.0 °C

Astragaloside I

Astragaloside I is a natural product isolated from Astragalus.

  • CAS Number: 84680-75-1
  • MF: C45H72O16
  • MW: 869.04
  • Catalog: Others
  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 910.6±65.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 265.5±27.8 °C

alpha-Cyperone

Alpha-cyperone is associated with the down-regulation of COX-2,IL-6,Nck-2,Cdc42 and Rac1, resulting in reduction of inflammation. which would be highly beneficial for treatment of inflammatory diseases such as AD.In vitro: The anti-inflammatory activity of alpha-cyperone is associated with the down-regulation of COX-2 and IL-6 via the negative regulation of the NFκB pathway in LPS-stimulated RAW 264.7 cells.[1]Alpha-Cyperone binds and interacts with tubulin and is capable of distinctly destabilizing microtubule polymerization. The effect of this interaction could result in reduction of inflammation which would be highly beneficial for treatment of inflammatory diseases such as AD. One microliter of alpha-Cyperone was dissolved in DMSO (1:1 v/v) and it was further diluted in double distilled water (ddH2O) to a final volume of 20 microliter. [2]

  • CAS Number: 473-08-5
  • MF: C15H22O
  • MW: 218.335
  • Catalog: Monoamine Oxidase
  • Density: 1.0±0.1 g/cm3
  • Boiling Point: 320.4±22.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 142.8±13.2 °C