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Sclareol glycol, a diterpene diol, is utilized as a precursor in the synthesis of ambroxide. It is characterized by a specific stereochemistry at its (3S,6R,8aS)-configurations, with two hydroxyl groups attached at the [2R,3aR,6S,8aR]-octahydro-3a,6,6,8a-tetramethyl-2-(1-methylethyl) perhydrophenanthrene framework.

1. Octyl Gallate is an antioxidant approved by the US Food and Drug Administration (FDA) as a food additive. 2. Octyl Gallate has antimetastatic activity. 3. Octyl Gallate shows antimicrobial activity against H. pylori, with a minimum inhibitory concentration (MIC) value of 125 ug/mL. 4. Combination therapy with octyl gallate and ferulic acid improves cognition and neurodegeneration in a transgenic mouse model of Alzheimer's disease.5. Octyl Gallate is a potential anticancer agent, it exhibited decreased MCF-7 & MDA-MB-231 survival and induced apoptosis, with IC50 value of 40 uM. 6. Octyl gallate (Octyl 3,4,5-trihydroxybenzoate) has antiviral activity, it shows an inhibitory effect on the growth of herpes simplex virus type 1 (HSV-1) in HEp-2 or Vero cells. 7. Octyl gallate shows antifungal activity against Saccharomyces cerevisiae ATCC7754 and Zygosaccharomyces bailii ATCC 60483.

Undecanal exhibits inhibitory activity against Saccharomyces cerevisiae ATCC, Candida albicans, and fungi, and is widely used in biochemical experiments and drug synthesis research.

Spirolaxine, a natural product isolated from Sporotrichum laxum ATCC 15155, has shown a variety of biological activities including promising anti-Helicobacter pylori property.

Herboxidiene (GEX1A) is a plant-toxic polyketide compound isolated from Streptomyces ATCC 49982, with herbicidal, cholesterol-lowering, and anticancer activities. It exhibits anti-angiogenic activity by downregulating vascular endothelial growth factor receptor-2 (VEGFR-2) and hypoxia-inducible factor-1α (HIF-1α).

N-acetyltyramine is a metabolite of the biogenic amine tyramine . It enhances cytotoxicity of doxorubicin in resistant P388 murine leukemia cells with an IC50 value of 0.13 μg ml compared with an IC50 value of 0.48 μg ml for doxorubicin alone.

Obafluorin is a β-lactone antibiotic produced by Pseudomonas fluorescens ATCC 39502, with broad-spectrum antibacterial activity, inhibiting tRNA transglycosylase, used in metabolic disease research.

4(1H)-Quinolinone, 1-methyl-2-(5Z)-5-undecen-1-yl- (compound 2), a quinolone alkaloid extracted from Cnidium, demonstrates activity against methicillin-resistant Staphylococcus aureus (MRSA), with minimum inhibitory concentration (MIC) values of 32 μg mL (ATCC 33591) and 16 μM mL (ATCC 25923) respectively [1].

3-O-Methylellagic acid, a natural product isolated from Myrciaria cauliflora, exhibits anti-inflammatory and antibacterial activities. This compound not only inhibits glucose transport but also demonstrates a minimum inhibitory concentration (MIC) of 32 μg mL against Staphylococcus aureus ATCC 25923 [1] [2] [3].

Majoranaquinone demonstrates potent antibacterial activity against four Staphylococcus strains, one Moraxella strain, and one Enterococcus strain. It also acts as an effective efflux pump inhibitor in Escherichia coli ATCC 25922 and inhibits biofilm formation on both E. coli ATCC 25922 and E. coli K-12 AG100 [1].

Maximin H1, an antimicrobial peptide sourced from the skin secretions of the Chinese red belly toad (Bombina maxima), exhibits efficacy against several pathogens, including Escherichia coli (ATCC25922), Staphylococcus aureus (ATCC2592), Bacillus pyocyaneus (CMCCB1010), and Candida albicans (ATCC2002). Corresponding minimum inhibitory concentration (MIC) values are 9, 4.5, 9, and 4.5 μg ml, respectively [1].

Maximin H3, an antimicrobial peptide from Chinese red belly toad Bombina maxima skin secretions, exhibits antimicrobial properties against Escherichia coli ATCC25922, Staphylococcus aureus ATCC2592, Bacillus pyocyaneus CMCCB1010, and Candida albicans ATCC2002, with respective MIC (Minimum Inhibitory Concentration) values of 20, 10, 20, and 5 μg ml [1].

FLGFVGQALNALLGKL-NH2, an antimicrobial peptide derived from frogs, exhibits activity against Staphylococcus aureus ATCC 29213 with a minimum inhibitory concentration (MIC) of 32 μM [1].

Mycestericin C, isolated from Mycelia sterilia ATCC 20349 culture broth, inhibits lymphocyte proliferation in the mouse allogeneic mixed lymphocyte reaction [1].

Eupenifeldin, a pentacyclic bistropolone isolated from Eupenicillium brefeldianum ATCC 74184, exhibits cytotoxic activity against the HCT-116 cell line and holds potential for leukemia research [1].

Glucoallosamidin A is a glycoside antibiotic that inhibits chitinase activity. It effectively suppresses the chitinase enzyme in Candida albicans [ATCC 10231], exhibiting an IC50 of 3.4 μg/mL.

Clavariopsin B is a cyclic peptide antibiotic exhibiting antifungal activity. It is effective against Candida albicans [IFO 0583], Candida albicans [ATCC 10231], Aspergillus niger [AJ117374], Aspergillus fumigatus [AJ117190], and Aspergillus fumigatus [JCM1739], with minimum inhibitory concentrations (MICs) of 8, 8, 16, 4, and 4 μg/mL respectively.

Glucoallosamidin B is a glycoside antibiotic identifiable in the Streptomyces species strain (Streptomycessp. SA-684). It functions as an inhibitor of chitinase activity. Experiments demonstrate that Glucoallosamidin B significantly inhibits the chitinase of Candida albicans (ATCC 10231), with an IC50 value of 0.8 μg/mL.

Cuevaene A can be isolated from the Streptomyces genus gdmAI-disrupted LZ35 strain. It exhibits moderate activity against Gram-positive bacteria, such as Bacillus subtilis (strain ATCC 11060), and demonstrates moderate activity against fungi, including Fusarium verticillioides (strain S68) and Rhizoctonia solani (strain GXE4).

Cuevaene B can be isolated from the Streptomyces genus gdmAI-disrupted LZ35 strain. This compound exhibits moderate activity against Gram-positive bacteria, such as Bacillus subtilis (strain ATCC 11060), and shows moderate activity against fungi, including Fusarium verticillioides (strain S68) and Rhizoctonia solani (strain GXE4).

Istamycin Y0 is an aminoglycoside antibiotic found in *Streptomyces tenjimariensis* [ATCC 31603]. This compound exhibits weak antibacterial activity against only a limited range of bacteria.

Clavariopsin A is a cyclic peptide antibiotic with antifungal properties. It exhibits activity against Candida albicans (IFO 0583 and ATCC 10231), Aspergillus niger (AJ117374), Aspergillus fumigatus (AJ117190), and Aspergillus fumigatus (JCM1739) with minimum inhibitory concentrations (MIC) of 8, 8, 16, 2, and 4 μg/mL, respectively.

Neihumicin exhibits resistance against the yeast Saccharomyces cerevisiae (ATCC 9763) and the mold Penicillium italicum (Wehmer), but it does not show resistance to bacteria.

Ala0-Actagardine is a woolly antibiotic (antibiotic) that can be found in the culture of the actinomycete [ATCC 31048].