Table 8.

¹³C-NMR data of pentacyclic triterpenoids classified as others isolated from Celastraceae species (2001–2021).

C	OT3	OT4	OT5	OT6	OT7	OT8	OT9 a	OT10 a	OT11 a	OT12
1	39.6	38.9	104.6	18.2	37.8	37.2	104.5	106.2	121.3	36.6
2	34.2	27.5	144.7	27.8	27.1	194.7	147.5	146.9	182.0	34.8
3	218.2	78.4	144.2	76.3	79.0	200.1	144.2	144.4	182.2	217.1
4	47.4	39.0	118.0	40.8	38.7	123.8	118.1	128.7	131.4	47.6
5	54.9	55.3	129.8	141.6	55.5	154.8	129.8	117.6	142.1	53.2
6	19.7	18.5	122.5	122.0	18.8	75.0	122.6	121.6	121.3	26.3
7	33.7	33.4	127.9	23.5	41.3	122.9	127.9	130.0	153.2	22.6
8	41.6	41.7	131.3	47.8	38.9	154.0	131.3	141.7	47.6	41.0
9	49.6	50.4	135.6	34.8	49.2	51.6	135.3	132.2	144.8	147.4
10	36.8	37.2	129.5	49.6	38.0	71.6	129.5	131.8	158.2	39.3
11	21.6	21.1	25.5	34.6	17.5	28.2	29.3	129.0	128.3	115.6
12	23.9	24.0	32.8	30.5	37.7	29.5	35.9	138.1	38.9	36.1
13	49.6	49.5	102.5	37.7	36.0	38.2	54.5	44.1	41.6	36.7
14	42.1	42.1	43.6	39.5	158.0	40.3	156.8	49.0	43.2	38.2
15	32.6	33.7	38.8	32.5	116.9	28.5	34.1	31.3	24.8	29.6
16	21.6	21.7	40.2	35.7	33.6	35.6	41.4	38.8	38.6	35.8
17	54.9	54.9	42.6	30.5	37.6	30.7	41.6	32.4	33.2	42.8
18	44.7	44.8	46.0	41.9	48.0	43.4	50.4	43.2	48.2	52.0
19	41.9	41.9	32.8	39.3	31.1	30.6	36.8	32.7	32.6	20.1
20	27.3	27.4	40.2	33.1	33.8	41.7	41.9	41.9	41.7	28.2
21	46.4	46.5	36.8	29.5	28.1	29.9	30.8	31.0	31.1	59.6
22	148.6	148.6	36.9	27.9	35.3	35.9	35.5	36.2	34.5	30.7
23	26.6	28.2	11.6	28.9	28.0	9.5	11.6	11.6	11.2	22.0
24	21.1	15.7		25.4	15.5					25.5
25	15.7	16.7	20.5	16.1	15.4	27.0	20.7	19.5	27.7	21.6
26	16.4	15.9	23.2	18.1	25.9	21.5	28.0	20.1	20.5	16.9
27	16.6	16.7	23.2	20.4	21.1	28.7	108.3	23.4	20.5	15.3
28	16.1	16.1	25.1	32.0	29.9	31.7	31.3	31.7	31.8	13.9
29	110.1	110.2	180.5	74.4	73.9	178.8	184.7	183.6	183.2	22.1
30	25.0	25.0	26.3	26.0	24.6	32.5	25.9	32.5	34.0	23.0
Ref	[94]	[94]	[139]	[213]	[213]	[250]	[139]	[139]	[139]	[251]
C	OT13	OT14	OT15	OT17	OT18	OT19	OT20	OT21
1	110.7	110.6	98.9	38.5	18.2	23.6	36.1	38.1
2	163.7	163.7	143.2	27.4	27.8	18.1	27.8	27.3
3			178.1	79.0	76.3	76.2	79.0	79.2
4	24.7	28.2	40.1	39.0	40.8	39.2	39.6	39.1
5	103.7	105.6	43.3	55.7	141.7	141.6	52.3	55.7
6	126.4	125.8	28.2	18.3	122.0	121.9	21.4	19.0
7	115.9	115.9	17.3	34.7	23.8	27.7	26.7	35.3
8	161.1	160.4	47.7	40.8	45.7	43.0	41.0	38.9
9	39.6	39.5	38.8	51.3	34.8	34.8	148.9	48.9
10	165.2	166.1	47.8	37.3	49.7	46.6	39.1	37.9
11	33.4	33.3	33.9	21.2	29.9	34.6	114.3	17.7
12	29.7	29.7	28.7	26.2	29.7	30.3	36.0	35.9
13	40.5	40.3	38.9	39.0	38.4	37.7	36.8	37.9
14	44.1	44.1	37.6	43.4	38.6	40.7	38.2	158.1
15	28.4	28.4	28.8	27.6	34.3	32.0	29.7	117.0
16	35.5	35.5	35.9	37.7	36.3	35.9	35.9	36.9
17	38.2	38.2	30.1	34.4	32.9	30.0	43.0	38.1
18	43.4	43.4	44.2	142.8	44.7	47.4	52.1	49.4
19	32.0	32.1	30.2	129.8	35.8	35.1	20.2	41.4
20	41.9	41.9	40.3	32.3	34.5	28.2	28.2	29.0
21	213.8	213.7	29.9	33.4	74.7	33.0	59.6	33.9
22	52.5	52.5	36.2	37.4	46.3	38.9	30.8	33.2
23			7.9	28.0	25.4	28.9	28.2	28.1
24			99.4	15.4	28.9	25.4	15.6	15.6
25	36.8	36.5	17.5	16.1	16.6	16.2	22.1	15.6
26	22.5	22.5	15.9	16.7	17.0	18.4	17.0	30.1
27	19.7	19.8	17.2	14.6	19.1	19.6	15.3	26.0
28	32.5	32.6	31.6	25.3	33.1	32.4	14.0	30.1
29			179.0	31.3	32.3	34.6	23.0	33.5
30	15.1	15.1	31.8	29.2	24.6	32.0	22.2	21.5
OCH3	50.5	51.0	51.3
Ref	[252]	[252]	[196]	[220]	[196]	[157]	[253]	[254]

Ref: References; NR: Not reported; Solvent CDCl₃; ^a CD₃OD; ¹³C-NMR data of some compounds were not found. In these cases, the reported identification was performed by comparison of other physical data: OT1 (m.p., [α]_D, IR, ¹H-NMR) [255], OT2 e OT16 (m.p., [α]_D, IR, ¹H-NMR, MS) [256].