Table 5.

Cluster comparisons.

Compound	LoVo							2008					MCF7								Reported Cytotoxic Activity
	I1	L1	L2	L3	L4	T1	S	I1a	L1a	L2a	L3a	T2	I1b	L1b	L2b	L3b	L4a	T3	V1	S
spathulenol																					[42]
endoborneol
p-cymene																					[15]
bornyl acetate
δ-carene
α-pinene
β-pinene
α-terpineol																					[17]
1-4 terpineol																					[15,46]
cterpinene
γ-terpinene																					[15,17]
β-phellandrene
γ-eudesmol
sabinene
2-nonanone
α-phellandrene
2-undecanone
β-eudesmol
α-copaene																					[17]
α-cadinol
T-cadinol
cadina-1,4-diene
β-elemene																					[8]
α-amorphene
germacrene A
α-muurolene
α-elemene
alloaromandrene
Octanoid acid
germacrene D
α-cubebene
β-cubebene
α-ylangene
1-phellandrene
BHT 1
α-cadinene
tricyclene
α-humulene																					[18]
trans β-ocimene
cis ocimene
d-limonene																					[8,15]
β-caryophyllene																					[8]
BMTTHU 2
HMHMOH 3
CPA 4
camphene

I (integerrima); L (lentiscus); T (terebinthus); V (vera); S = single, unclustered bioactivity-correlated compounds. ¹ Butylated hydroxy toluene; ² Benzene-methoxy-trimethyl-tetrahydro-halenedica-urs-12-en-28-al; ³ 4,12-bis(hydroxymethyl)-2,2-metac-4,14-bis(hydroxymethyl)-2,2-metac-1-oxo-2,3,5,6,7,8-hexahydrothienol; ⁴ 4-chloro-2-phenylaniline.